ebook img

Molecular and Cellular Endocrinology 1996: Vol 116-125 Index PDF

21 Pages·1996·4.6 MB·English
by  
Save to my drive
Quick download
Download
Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.

Preview Molecular and Cellular Endocrinology 1996: Vol 116-125 Index

Molecular and Cettuiar : “Ga4 Endocrinology ELSEVIER Molecular and Cellular Endocrinology 126 (1997) 225-231 Cumulative keyword index Volumes 116—125 (1997) A10 cells 122, 93 Apoptosis 119, 61 Acetyl-CoA 120, 115 Arachidonic acid 118, 193 ACTH 121, 65; 124, 97 Aromatase 118, 217 ACTH receptor 121, 57 ATP-citrate lyase 120, 115 Activin 116, 105; 121, 1; 122, 21 Atrial natriuretic peptide phosphopeptide mapping 122, 159 Activin receptor 116, 105 Atrial natriuretic receptors 117, 189 Acyl-CoA-binding protein 118, 65 AtT20 120, 1 Ad4BP 124, 97 AtT-20 120, 161 Adenohypophysis 123, | Autocrine 124, 63 Adenosine 117, 17; 118, 47 Autocrine regulation 119, 95 Adenosine receptor 117, 17 Avidin-biotin 119, 69 Adenylate cyclase 124, 141 AVP gene promoter 123, 179 Adipokinetic hormone 116, 199; 122, 141; 123, 97 AVP mRNA 123, 179 Adipose 118, 217 AVP release 123, 179 ADP ribosylation 123, 139 Azide 121, 165 Adrenal 121, 87; 122, 151 Adrenal cells 121, 65 Baculovirus expression 117, 95 Adrenal gland 117, 189 Basal transcription machinery 120, 85 B-Adrenoceptor 117, 7 bel-2 119, 61 Adrenocorticotropin 116, 89 Benign breast disease 121, 11 Adult 120, 51 Bioassay of gonadotropins 118, 145 Age 116, 233; 124, 110 Biologic activity 125, 71 Aging 118, 181; 123, 127 Blattella germanic 121, 191 All 124, 97 Boar 123, 61 Aldose reductase 124, 79 Bone marrow 117, 183 Aldosterone 119, 105 Bovine 120, 25 Aldosterone synthase 121, 87 Bovine adrenal fasciculata cells 124, 97 Allatostatin 122, 183, 191 Bovine adrenocortical cells 121, 57 Allatostatins 121, 191 Brain-derived neurotrophic factor 116, 149 Alpha-fetoprotein 118, 15 Breast 118, 15 Alternate splicing 120, 25 Breast cancer 118, 217; 121, 11 Alternative splicing 125, 169 Breast cancer (human) 117, 211 Amidation 123, 113 Brown adipocytes 117, 7; 121, 37 Amiloride 116, 73 Brown adipose tissue 116, 59; 121, 37 Amnion 117, 141 Anaplastic carcinoma 121, 143 Ca2+ 120, 1 Androgen 117, 53; 121, 11, 75 [Ca2 + ]i oscillations 123, 163 Androgen insensitivity syndrome 120, 15 Calcitriol 116, 149 Androgen receptor 116, 137, 233; 120, 15, 51; 121, 75; 123, 89; 124, Calcium 116, 199; 117, 1; 121, 87; 124, 185 110 Calcium channels 119, 129 Androgen receptor mRNA 116, 233; 124, 110 Calcium-dependent protease 122, 81 Androgen regulation 124, 79 calmodulin kinase 120, | Androgen-responsive element 120, 15 Calpain 122, 81 Androgens 118, 65; 121, 197 Calpain inhibitors 122, 81 Androsterone 118, 95 Calpastatin 122, 81 Angll 121, 65 cAMP 116, 39, 165, 173; 118, 193; 120, 1, 99, 125; 121, 1; 124, 71, 141 Angiotensin II 119, 105; 121, 87; 122, 93 cAMP-dependent transcription 117, 167 Angiotensin receptors 122, 59 cAMP signalling pathway 119, 129 Anterior pituitary 119, 195; 122, 159; 124, 121 Carbohydrate response 123, 37 Anti-GBM antibody 123, 205 Carbohydrates 125, 101 Anti-peptide antibodies 125, 79 Carboxypeptidases E 117, 219 Anti-RXR antibody 121, 179 Cardiomyocytes 120, 107 Antisense 116, 89; 118, 113 B-Casein activation 123, 17 AP-1 119, 25; 122, 151; 123, 71; 124, 51 Castration 119, 123; 121, 153 226 Cumulative keyword index vols. 116—125 (1997) (Cattle) 116, 191 Differential hybridization 123, 199 CCCP 121, 165 Differentiation 117, 17; 120, 169; 122, 59 cDNA 122, 191; 124, 185 25-Dihydroxyvitamin D3 116, 149 cDNA isoform 116, 207 Disulfide bridge 117, 59 cDNA libraries 123, 199 DNAase I sensitivity 118, 155 cDNA sequence 123, 45 DNA binding 120, 85 B-Cell 117, 1; 119, 185 DNA-binding domain 120, 15 Cell cycle 116, 115, 227 DNA binding domain mutant 120, 85 Cell-free transcription 122, 15 DNA damage 118, 71 B-Cells 118, 71 DNA polymorphisms 117, 253 Cell surface 119, 69 DNA response element 116, 213 Cellular heterogeneity 118, 181; 123, 127 DNA sequencing 118, 173 c-erbA 116, 59 Dolichol 122, 223 c-fos 116, 233; 117, 233; 119, 25, 75; 120, 1; 123, 71; 124, 33, 110 Domain structure 116, | c-fos mRNA 116, 233; 124, 110 Dopamine 124, 121 cGMP-dependent protein kinase 122, 159 Double stranded RNA 118, 37 Chimpanzee 118, 85 Down regulation 118, 103 Chloramphenicol acetyl transferase (CAT) 118, 25 (Drosophila melanogaster) 116, 73 Cholinergic 119, 185 3-D structure 125, 21 Chondrocytes 123, 27 Dual opposing effects 123, 149 Choriocarcinoma 124, 63 Choriogonadotropin 122, 173; 125, 107 Ecdysteroidogenesis 120, 99 Chorionic gonadotrophin 122, 51 Ectodomain 125, 79 Chorionic somatomammotropin 119, 1 EGF 123, 61, 89 Chromaffin cells 119, 175 EGF receptor 123, 61 Chromatin 118, 155 Egr-1 117, 167 Chromogranin A 124, 51 Electrophysiology 123, 163 c-jun 117, 233; 119, 25, 75 Embryonic development 118, 113 Cloning 121, 153 Endocrine regulation 123, 113 Cloprostenol 123, 45 Endodomain 125, 79 c-myc 119, 61 Endometrial carcinoma 118, 173 Cockroach 116, 199; 123, 97 Endometrium 117, 233; 118, 173; 120, 193 Collagen 123, 27 B-Endorphin 116, 89 Comet assay 118, 71 Endozepine 122, 69 Competitive RT-PCR (fetal sheep) 117, 101 Enhancer 119, | Concanavalin A 118, 37 Enterocytes 119, 129 Constitutive activity 119, 161 Enzyme turnover 117, 211 Cornifin 123, 7 Epidermal growth factor 118, 125; 124, 63 Corpora allata 122, 183 Epidermal growth factor receptor 117, 53 Corpus luteum 120, 25; 122, 213; 123, 45 Corticotroph 119, 25 Epithelium 117, 247 Epitope 122, 51 CpG island 120, 193 CRF 119, 25 Epitopes 125, 33 C-terminus 125, 93 Equine 125, 3 Culture 117, 141 Erythropoietin 117, 101 Culture model 120, 169 Estradiol-178 119, 37 Cyclic adenosine-3’ 119, 207 Estradiol 116, 191; 117, 211; 124, 71, 87 Cyclic AMP 117, 17; 119, 161 178-Estradiol 119, 129 Cycloheximide 116, 233; 121, 57; 124, 110 Estrogen 117, 219; 118, 15; 120, 41; 121, 11, 29; 122, 213; 123, 7; 124, CYP2C2 120, 77 173 Cystatin-related protein 121, 197 Estrogen receptor 118, 173; 119, 37, 47; 120, 177; 121, 153; 123, 149; Cytochrome P450 cholesterol side-chain cleavage mRNA 117, 203 124, 173 Cytokine 121, 11 Estrogen regulation 117, 241 Cytokines 118, 217 Eukaryotic cell 116, 1 Cytosolic free calcium 119, 105 Evolution 124, 163 Exoloops 125, 93 Dehydrogenase/isomerase 116, 157 Expression 117, 59; 124, 43 Delayed hormone response 123, 187 Extracellular domain 125, 65 Desensitization 116, 39; 117, 75 Extragenomic action 117, 83 Determinant loop 124, 151 Extra-pituitary (rat placenta) 118, 9 Development 116, 157 Developmental expression 120, 147 Fat body 116, 199; 121, 191; 122, 15 Dexamethasone 120, 153 Fatty acids 119, 219 Diabetes mellitus 116, 67 Fetal 120, 51 Diamide 121, 165 Fetal sheep 119, 113 Diazepam-binding inhibitor 118, 65 Fetal tissue response 116, 49 Diethylstilbestrol 118, 1, 207 FGF 18, 113 Cumulative keyword index vols. 116—125 (1997) Fibroblast 117, 141 Gonadotropin structure/function 124, 151 Fibrosis 124, 7 G-protein-coupled receptors 125, 65 Fischer 344 rats 118, 207 G-protein-linked seven transmembrane domain receptor 120, 147 Fish 124, 131 G proteins 122, 207; 123, 139 Flow cytometry 118, 163 Gaq/Gall mRNA and protein 121, 65 Fluo-3 118, 163 Granulosa cell 120, 25 Fluvastatin 121, 191 Granulosa cells (pig) 117, 203 Follicle-stimulating hormone 125, 151 Graves’ IgG 118, 47 Follicle stimulating hormone 122, 21 GRE 123, 187 Follicle-stimulating hormone receptor 125, 177 Gross cystic disease fluid protein 121, 11 Follicular carcinoma 116, 115 Growth 121, 143; 122, 59 Follistatin 116, 105; 121, 1 Growth factor 117, 111; 124, 131 Forskolin 118, 193 Growth hormone 118, 95, 181; 120, 77; 123, 127 Fragment 125, 107 Growth hormone and chorionic somatomammotropin gene family Free radicals 121, 101 118, 155 FSH 116, 39; 118, 37; 124, 151; 125, 133 Growth hormone family 119, | (FSH) 125, 151 Growth hormone receptor 116, 223 FSH-receptor 120, 25 Growth hormone (somatotropin 117, 75 FSH receptor 124, 151; 125, 151, 161, 169 Growth promotion 116, 223 FSH receptors 122, 199 GTP 123, 139 FSH-responsive granulosa cell line 116, 39 GTP binding proteins 119, 195 FSH responsive granulosa cell line 118, 145 B-Hairpin loops 122, 173 GC-rich promoter 117, 167 Haploid gene expression 122, Gelatinase 118, 37 Harderian gland 124, 87 hCG 125, 79, 107 Gel mobility shift assay 121, 47 Gel shift assay 120, 85 hCG-receptor complexes 125, 79 hCG secretion 118, 125 Gene expression 116, 31, 81; 117, 121, 175, 241; 118, 113; 119, 147; 120, 67, 133; 121, 153; 123, 71; 124, 51, 71 Hematopoiesis 120, 59 Hemolymph protein 122, 15 Gene mapping 117, 253 Hemorrhage 117, 101 Gene organization 125, 177 Hepatocytes 119, 219; 123, 37 Gene promoter 120, 203 Hepatoma 121, 179 Gene regulation 117, 27; 119, 1 Heterodimerization 125, 45 Gene sequence 120, 177 Hexamethylenebisacetamide 117, 111 Gene structure 118, 85 HGF 117, 247 Gene structure (mouse) 124, 25 HL-60 cells 120, 147 Genomic sequencing 117, 253 Homodimer 119, 11 Germ cells 122, 69 Hormone action 119, 147 Gestation 116, 49 hpg mice 125, 169 efg 118, 113 H295R cell (human) 118, 137 GH3 120, 161 11B-HSD2 gene 119, 113 GH 116, 181 Human 118, 47, 85; 120, 51; 121, 87 (GH binding protein) 116, 181 Human breast epithelial cell line 119, 47 (GH receptor) 116, 181 Human choriogonadotropin (hCG) 125, 55 GIP 116, 81 Human chorionic gonadotropin 125, 33, 121 Glomerulonephritis 123, 205 Human chorionic gonadotropin (hCG) 125, 21 Glucocorticoid 121, 11 Human corpus luteum 124, 141 Glucocorticoid receptor 116, 137; 120, 139; 121, 75 Human estrogen receptor gene 116, 207 Glucocorticoids 117, 141; 121, 197; 122, 151 Human follitropin 125, 45 Glucokinase 117, 175 Human GnRH 117, 241 Glucose (rat islets of Langerhans) 117, 195 (Human granulosa cell) 121, | Glucose sensitivity 116, 81 Human granulosa lutein cells 120, 169 Glucose-stimulated 123, 199 Human luteinizing hormone 125, 121 Glycogen phosphorylase 116, 199 Human melanocytes 116, 131 Glycoprotein 125, 101 Human spermatozoa 117, 83 Glycoprotein hormone 122, 173 Human trophoblastic cells 118, 125 Glycoprotein hormones 125, 33 Hybrid hormone 125, 3 GnRH 117, 27 20-Hydroxyecdysone 116, 73 GnRH receptor 122, 33 11B-Hydroxysteroid dehydrogenase 120, 67 Goitre 121, 101 Hydroxysteroid dehydrogenases 121, 93 Gonadotrope cell line 122, 33 Hyperglycemic hormone 123, 97 Gonadotropin 122, 21 Hypertrehalosemic hormone 116, 199; 123, 97 Gonadotropin action 119, 207 Hypogonadism 125, 143 Gonadotropin bioassays 125, 151 Hypophosphatemia 124, 17 Gonadotropin-releasing hormone 119, 75 Hypothalamus 121, 153 Gonadotropin-releasing hormone (Gonadotropes) 118, 103 Gonadotropins 123, 163; 125, 3 IGFBP-2 120, 193 228 Cumulative keyword index vols. 116-125 (1997) IGFBPs 120, 193 Leydig cell 118, 57; 119, 135 IGF II 118, 201 (Leydig cells) 118, 193 (IGF-I Receptor) 116, 181 Leydig insulin-like peptide (Ley I-L) 121, 171 IGF-1 receptor 124, 131 LF-amide 117, 157 Immediate early gene 123, 205 LH 124, 141, 151; 125, 133, 143 Immortalized granulosa cells 123, 171 (LH) 125, 151 Immunoassay 125, 107 LH action 119, 135 Immunolocalization 125, 161 LH/CG receptor 117, 95; 125, 101 Imnunochemical mapping 125, 79 LH receptor 124, 151; 125, 79, 151, 161 Imperfect ERE 120, 177 Ligand binding assay 121, 47 Imperfect EREs 123, 149 Lipid peroxidation 121, 101 Infertility 125, 143 Lipopolysaccharide 118, 37 Inherited 125, 143 LIV-1 121, 29 ‘ Inhibin « 119, 135 Liver 116, 97, 157, 207; 119, 37 Inhibin 121, 1; 122, 21 Locust 122, 15 Inhibitory guanine-nucleotide-binding regulatory protein 120, 9 (Locust fat body) 122, 141 Inositol-1 116, 199 LPL 116, 97 Inositol phosphates 122, 141 LPL-extinction 116, 97 Insect 116, 199; 117, 157; 122, 141; 123, 97 LPS 117, 183 Insect neuropeptide 120, 115 Luciferase 119, 207; 121, 93 In situ hybridization 119, 147 Luteinization 120, 25 Insulin 116, 67, 81; 117, 1, 211; 120, 107, 139; 121, 29; 122, 93; 123, Luteinizing hormone 119, 207; 122, 213; 125, 151 37 Luteinizing hormone (LH) 125, 55 Insulin growth factor-I 118, 95 Luteinizing hormone secretion 123, 163 Insulin-like growth factor-1 117, 211; 123, 27 Lysosomal enzymes (human hepatoma cells) 118, 201 Insulin-like growth factor binding proteins 120, 59 Insulin-like growth factors 120, 59 Macrophages 124, 7 Insulin receptor 122, 131 Maldi-TOF 122, 183 Insulin receptor substrate-1 (IRS-1) 122, 131 Male reproductive tract 123, 89 Insulin release 118, 71 Male-specific 120, 77 Insulin resistance 119, 219 Mannose 6-phosphate/IGF II receptor 118, 201 Insulin secretion 117, 195; 119, 185; 121, 133 Maps 125, 33 Interaction 125, 65 MCF-7 121, 29 Interferon-y activation sequence 121, 19 Melanocortin receptor 116, 131 Interferon regulatory factor-1 121, 19 Melanogenesis 116, 131 Interleukin-6 124, 33 Melatonin 117, 183; 123, 53, 71, 139 Interleukin-2 124, 33 Mercaptoethanol 121, 165 Interleukin-! 118, 37 Met 117, 247 Interleukin 121, 11 Methoprene 122, 15 Intermolecular regulation 116, 1 Metyrapone 122, 151 Intestinal estrogen receptors 121, 47 Mevalonate 121, 191 Intestine 119, 129 Micronuclei 117, 183 Intracellular calcium 118, 47; 124, 121 Microsatellites 117, 253 Intramolecular regulation 116, 1 Milk 117, 41 IRS-1 122, 81 Modelization 116, 137 Islets of Langerhans 121, 133 Molecular activation 116, | 3-Isobutyl-1-methylxanthine 117, 203 Moleculai cloning 124, 25 Isoforms 120, 51 Monkey GnRH 117, 121 Monoclonal antibodies (mAb) 125, 79 Jak2 123, 17 Monoclonal antibody 116, 223; 122, 51 Janus kinase 117, 131 5'-monophosphate 119, 207 Japanese eel 119, 37 Morphology 116, 131 JunB 122, 151 Morphometrics 119, 123 Juvenile hormone 120, 115; 122, 183 Mosquito USP isoforms 121, 119 Mouse embryo 124, 185 Ketosteroid reductase 116, 157 (Mouse 3BHSD genes) 116, 157 Kidney 120, 67 Mouse kidney 119, 147 mRNA 116, 181; 117, 101; 118, 37, 85, 181; 121, 171; 124, 131; 125, Labor 117, 141 169 Lacrimal gland 120, 133; 121, 197 mRNA distribution 119, 113 Lactate 121, 165 y-MSH 116, 89 Lactating rat 124, 121 MSH 116, 131 Lactoglobulin 118, 25 Multiple transcripts 120, 177 Lactotroph cell 124, 121 Multiple urinary forms 125, 121 Large T antigen 117, 167 Muscle 124, 131 Larval-pupal transformation 120, 99 Mutagenesis 117, 59 Leiomyoma 117, 233 Mutation 125, 143, 177 Cumulative keyword index vols. 116-125 (1997) Mutations 124, 43 P450arom 119, 69 Myoblasts 122, 207 Pars tuberalis 123, 71 Myometrium 117, 233; 120, 125, 193 Parturition 120, 125 Myotropin 117, 157; 122, 183, 191 PCR 387, 175 Myristoylated pseudosubstrate peptides 121, 133 PC12W cells 122, 59 PD123177 Losartan 122, 59 NAD(P)H autofluorescence 118, 163 Peptide biosynthesis 116, 89 NADPHP450 reductase 119, 69 Peptide hormones 123, 113 Na+/H+ exchange 116, 73 Peptide mapping 125, 79 Natriuretic peptide 118, 137 Peptides 118, 15 Nb2 T cells 121, 19 Peripheral blood 117, 183 Negative regulation 120, 139 Peroxisome proliferator 120, 31 Neobellieria 117, 157 Pertussis toxin 118, 193 Neonatal 116, 97 PGE2 122, 101 Neonatal Immunity 117, 41 PGHS2 122, 101 Neonatal ovary 122, 21 Phage display 125, 21 Neonate 117, 75 Phenobarbital 120, 77 Nephrogenic diabetes insipidus 124, 43 Phorbol ester 117, 75, 203; 119, 185 Nerve growth factor 116, 149 Phosphatidylinositol 3-kinase 122, 131 Nerve growth factor receptors 116, 149 Phosphoinositide 122, 141 Neuroendocrine 124, 51 Phospholipase-A2 122, 33 Neuropeptide 117, 157; 122, 183, 191 Phospholipase-C 122, 33 Neuropeptide Y 120, 161 Phospholipase C 122, 141, 207 Neurotrophin 116, 149 Phospholipase-D 122, 33 NF-«B 121, 75 Phospholipase D 122, 207 NGFI-B 123, 205; 124, 97 Phosphoprotein substrates 122, 159 Nitric oxide 118, 71 Phosphorylation 119, 185 NMR 125, 21 Phospho-serine/threonine phosphatase 117, 195 NOR-1 123, 205 Photolabeling 125, 93 NPY 120, 161 Photoperiod 123, 53 Nuclear IGF-I receptor 118, | Photoperiodism 121, 153 Nuclear receptor 119, 37; 123, 53 Physical parameters 125, 133 Nucleotide sequence 120, 147 Pig thyroid cells 119, 95 Nucleus 120, 107 pl6 (INK4a/MTS1) 116, 115 Nude mouse 121, 143 Pit-1 gene expression 118, 9 Pituitary 117, 219; 118, 155; 119, 61; 121, 153; 123, 53, 71 Ob1771 preadipocytes 117, 17 Pituitary adenomas 124, 33 25(OH)2-Vitamin D3 122, 207 Pituitary adenylate cyclase-activating polypeptide (PACAP) 117, 227 Oligomycin B 121, 165 Pituitary cell 123, 1 Oligosaccharide 125, 3 Pituitary gonadotropins 125, 133 Oligosaccharyltransferase 122, 223 PKC 124, 79 Oncogenic osteomalacia 124, 17 Placenta 118, 155; 119, 1; 121, 93 Ontogeny 117, 75 Placental lactogen-I variant 116, 49 Oreochromis aureus 120, 177; 123, 149 Placental lactogens 118, 9 Ornithine decarboxylase 117, 211 Polarized expression 125, 161 Orphan receptor 120, 31; 124, 97 POMC 119, 25; 120, 161 Osmotic and non-osmotic stimulation 123, 179 Porcine 120, 193 Qsteosarcoma 116, 149 Porcine anterior pituitary 119, 75 Ovarian follicle 116, 191 Porcine thyroid cells 122, 223 Ovary 117, 227; 121, 171; 124, 141; 125, 169 Post-source decay 122, 183 (Ovary) 116, 191 Post-translational processing 116, 89 Oviduct 122, 183 Potassium 119, 105; 121, 87 B-Oxidation 116, 213 Precursor 122, 191 Oxytocin 116, 191 Pregnancy 117, 189; 120, 125 Oxytocin receptor 124, 25 Primary cultures 121, 197 Progesterone 116, 191; 117, 27, 83; 123, 171 p53 119, 61 Progesterone receptor 119, 169 P45017x 119, 69 Prohormone convertases 116, 89 PACAP 117, 227 Prolactin 117, 41, 59, 131; 118, 25; 121, 19; 122, 101; 123, 53 PACAP receptor, type I isoforms 117, 227 Prolactin-inducible protein 121, 11 Pancreatic Bcells 117, 175 Prolactin receptor 117, 41, 131; 123, 17 Pancreatic islet B-cells 118, 163 Prolactin receptors 122, 199 Pancreatic islets 118, 71 Prolactin receptor signaling pathway 116, 49 Papillary carcinoma 116, 115 Proliferation 124, 7 Paracrine/autocrine regulation 118, 57 Proopiomelanocortin 120, 161 Paracrine function 119, 175 Prostaglandin E2 123, 27 Parathyroid hormone-like 124, 17 Prostaglandin F2« receptor (rat) 123, 45 230 Cumulative keyword index vols. 116—125 (1997) Prostaglandin H synthase 117, 141 (Salivary glands) 116, 73 Prostate cancer 117, 53 (Schistocerca gregaria) 122, 191 Prostatic binding protein 121, 197 Seasonality 123, 53 Protein kinase A 120, | Secondary steroid response 120, 153 Protein kinase-C 122, 33 Secretion 117, 59 Protein kinase C 116, 1; 119, 105, 185; 121, 133; 122, 213 Selenium deficiency 124, 7 Protein kinase C isoenzymes 118, 103 Sertoli cell 120, 41 Protein phosphatase 120, 107 Sertoli cells 122, 199 Protein-protein interaction 122, 131 (Sertoli cells) 117, 167 Protein substrate 116, | Serum 116, 173 Proteoglycans 118, 57 Sex steroids 121, 11 Proteolysis 121, 179 Sexual differentiation 123, 89 Prothoracicotropic hormone 120, 99 Sexual dimorphism 124, 87 pS2 121, 29 Sheep 121, 153, 171 Purine metabolism 119, 123 Signaling receptor for LH and hCG 125, 55 Pyruvate 121, 165 Signal transduction 116, 199, 227; 117, 131; 120, 99; 122, 141 Signal transduction pathways 120, 9 Rab proteins 119, 195 Silkworms 120, 99 Rat 116, 31, 181; 117, 189; 120, 125 Simian virus 40 120, 169 (Rat) 116, 67, 97 Single amino acid substitution 120, 15 Rat liver 119, 123 Site directed mutagenesis 122, 173 Rat pancreatic islets 123, 199 Slp 121, 75 rat pituitary) 117, 75 Small angle laser light scattering analysis 118, 145 Rat placenta 116, 49 Small intestine 116, 31 (Rats) 124, 7 Smooth muscle 116, 67; 120, 125 Rat SMGGP 120, 133 Sodium-dependent phosphate uptake 124, 17 Rat StAR 123, 171 Somatotropes (rat) 118, 181; 123, 127 Rat testis 120, 9 Somatotropin-releasing hormone 117, 75 (Rat testis) 118, 37 Southern blot analysis 121, 47 Rat theca-interstitial cells 118, 95 Spermatogenesis 122, 69; 123, 61 Rat ventral prostate 116, 233; 124, 110 sPLA2I 122, 101 Receptor 116, 227; 118, 137; 120, 147; 124, 43; 125, 3 Splenocytes 117, 41 Receptor binding 125, 45 Spliced variants 118, 173 Receptor crosstalk 116, 213 Sprague-Dawley rats 118, 207 Receptor interaction 125, 93 Squamous differentiation 123, 7 Receptor phosphorylation 116, 39 Stanniocalcin 124, 185 Receptor-positive type 120, 15 Stat 121, 19 Receptors 117, 227 STAT transcription factor 117, 131 Reconstitution 125, 79 Staurosporine 116, 39; 118, 25 Red deer 123, 17 Steroid hormones 119, 129 Regulation 121, 65; 122, 223 Steroidogenesis 118, 57, 193; 120, 169; 122, 21 Relative K + conductance 116, 73 Steroid receptor 117, 27 Relaxin 118, 85; 121, 171 Steroids 124, 87 Releasing activity 123, 127 Steroid/thyroid hormone receptors 119, 147 Reproductive tissue 117, 121 Streptozotocin 116, 67 Response element 119, 11; 120, 31, 203 Stromal cells 120, 59 Ret 117, 247 Structure 125, 33 Retinoic acid 118, 125; 120, 203; 123, 7; 124, 163 Structure-function 125, 71 Retinoic acid receptor 118, 125 Structure-function relationship 116, 137 Retinoid receptors 121, 179 Subcellular distribution 119, 195 Rev-erbA 116, 59 a-Subunit 125, 21 Reverse hemolytic plaque assay 123, 163 o Subunit 125, 93 Reverse transcription-polymerase chain reaction 119, 75 Subunit 125, 107 Rho proteins 119, 195 B-Subunit seat-belt 124, 151 Riboflavin carrier protein 120, 41 Suckling 116, 97 RIN 1046-38 cells 116, 81 SV40 T-antigen 119, 135 RNA 118, 113 Synergism 123, 149 RNR-1 123, 205 Synthetic peptides 125, 79 Ro 20-1724 117, 203 Syrian hamster 124, 87 Rodents 118, 15 tRNA 118, 207 Tammar wallaby 119, 169 RT-PCR 118, 173; 121, 47; 123, 171 a“T3-1 cells 118, 103; 122, 33 RU486 resistance 119, 169 Testicular feminization 116, 137 RXR 119, 11 Testis 119, 135; 122, 69, 199; 123, 17, 61 Testis (rat testis) 118, 57 $14 123, 37 Testosterone 118, 37; 119, 123; 120, 9, 77 Saccharomyces cerevisiae 120, 31 Tethered gonadotropins 125, 71 Cumulative keyword index vols. 116—125 (1997) TGF 123, 61 Tri-iodothyronine 119, 219 TGF-B 117, 1; 124, 7 5-Trisphosphate 116, 199 Thermogenesis 117, 7 Trophoblast 120, 147 Thermogenin 117, 7 Trophoblast cell 116, 49 Thymocytes 117, 41 Truncated derivative 119, 69 Thyroglobulin 116, 165, 173; 122, 223 TRva2 120, 85 Thyroid 116, 115; 117, 111, 247; 119, 95; 121, 143; 124, Trypsin activation 119, 161 Thyroid cell 116, 165; 117, 111; 118, 47 TSH 118, 47 Thyroid cells 116, 173 TSH receptor 119, 161 Thyroid hormone nuclear receptor 119, 95 Tumorigenesis 118, 207 Thyroid hormone receptor 116, 59; 120, 85 Tumors 117, 219 Thyroid hormones 119, 95 Tumour suppressor genes 116, Thyroid receptor auxiliary protein 120, 85 Tyrosine kinase 117, 53; 124, | Thyroid response element 120, 85 Tyrosine kinase inhibitor 117, 53 Thyroperoxidase 121, 101 Tyrosine phosphorylation 117, 83; 118, 25 Thyrotropin 122, 223 Thyrotropin receptor 117, 253; 121, 143 Itrastructure 118, 181 Thyrotropin-releasing hormone 124, 121 ncoupling protein 116, 59; 117, 7 Tissue distribution 120, 51 rokinase 117, 167 Tissue renin 119, 175 terine stromal cells 122, 101 Tissue specificity 120, 133 Jteroglobin 124, 87 Tissue transglutaminase 120, 203 terus 118, 15, 173; 120, TPA 121, | Trans-activation 120, 85 Vagina 123, 7 Transcription 116, 213; 119, 207; 120, 153; 124, 163 Vascular smooth muscle 122, 93 Transcriptional regulation 119, 9 > 123, 187 Vasoactive intestinal peptide 116, 31 Transcription and rainbow trout 124, 173 Vasopressin 124, 43 Transcription factor 119, 75 Vitamin A 123, 7 Transcription signals 120, 177 Vitamin D3 124, 163 Transcription start site 116, 207; 117, 121 Vitamin D 116, 149 Transcytosis 125, 161 Vitellogenesis 121, 119 Transfection 117, 59; 119, 47; 124, 43, 51 Vitellogenin 121, 191; 124, 173 Transforming growth factor-f 116, 227 Voltage and DHP sensitive calcium channel 122, 3: Transgenic mice 120, 77 Transgenic Ren-2 rat 119, 175 Western blot analysis 121, 47 Transient transfection 123, 149 Western blotting 122, 51 Translocation 118, 103 White adipose tissue 116, 59 T3 receptors 121, 37 Wortmannin 118, 201 TR expression 121, 37 WTI 117, 167 . Molecular and )) GCettutar Endocrinology Molecular and Cellular Endocrinology 126 (1997) 233~—244 Cumulative author index Volumes 116 125 (1997) Abbaszade, I.G., see J. Park, C.-H. 116 157 Aydin, S., Oztiirk, Y., Melih Altan, V., Yildizoglu-An, N.. Ozcelikay. Adachi, S., see Todo, T. 119 37 A.T., Effect of insulin treatment on smooth muscle calmodulin Adams, L., see Wang, Y. 116 81 levels in rats with long-term streptozotocin-diabetes 116 67 Adiga, P.R., see Subramanian, S. 120 41 Azuma, C., see Kubota, Y. 124 25 Agarwal, A.K., White, P.C., Analysis of the promoter of the NAD + dependent 11/-hydroxysteroid dehydrogenase (HSDI1K) gene in Baes, M., see Castelein, H. 119 11 JEG-3 human choriocarcinoma cells 121 93 Bahl, O.P., see Shao, K. 122 173 Aharoni, D., see Schiffer, Z. 118 145 Baker, V.L., see Bousfield, G.R. 125 3 Ailhaud, G., see Borglum, J.D. 117 17 Baker, V.V., see Hu, C. 118 173 Aitken, R.J., Buckingham, D.W., Harkiss,, D., Paterson, M., Fisher, Balvers, M., see Pusch, W. 122 69 H., Irvine, D.S., The extragenomic action of progesterone on Bamberger, A.-M., Bamberger, C.M., Wald, M., Kratzmeier, M.., human spermatozoa is influenced by redox regulated changes in Schulte, H.M., Protein kinase C (PKC) isoenzyme expression pat- tyrosine phosphorylation during capacitation 117 83 tern as an indicator of proliferative activity in uterine tumor cells Albanesi, C., see Grimaldi, P. 117 167 123 81 Alcorn, D., see Berka, J.L. 119 175 Bamberger, C.M., see Bamberger, A.-M. 123 81 Alfthan, H., Stenman, U.-H., Pathophysiological importance of vari- Barrett, P., see Hazlerigg, D.G. 123 53 < ous molecular forms of human choriogonadotropin 125 107 Barrett, P., see Ross, A.W. 123 71 Allgeier, A., see Van Sande, J. 119 161 Bartsch, G., see Neuschmid-Kaspar, F. 117 149 Almadén, Y., see Dobado-Berrios, P.M. 118 181 Bauer, C.K., see Reid, G. 124 121 Alsat, E., see Roulier, S. 118 125 Beau, I., see Misrahi, M. 125 161 Alvarez, J., see Varriale, B. 124 87 Bech, K., see Krogh Rasmussen, A. 116 173 Amarneh, B.A., Simpson, E.R., Detection of aromatase cytochrome Bech, K., see Rasmussen, A.K. 116 165 P450, 17x-hydroxylase cytochrome P450 and NADPH:P450 reduc- Becker, M., Newman, S., Ismail-Beigi, F., Stimulation of GLUT] tase on the surface of cells in which they are expressed 119 69 glucose transporter expression in response to inhibition of oxida- Amphoux-Fazekas, T., see Fayet, G. 117 111 tive phosphorylation: role of reduced sulfhydryl groups 121 165 Amsterdam, A., see Keren-Tal, I. 116 39 Begeot, M., see Penhoat, A. 121 57 Amsterdam, A., see Schiffer, Z. 118 145 Behre, H.M., see Gromoll, J.o. 125 177 Amsterdam, A., see Selvaraj, N. 123 171 Bellés, X., see Martin, D. 121 191 Andersson, A.-C., see Gustavsson, B. 121 143 Ben-Menahem, D., see Sugahara, T. 125 71 Andrada, J., see Pereda, M.P. 124 33 Benahmed, M., see Caussanel, V. 123 61 Andreani, C.L., see Apa, R. 118 95 Benahmed, M., see Guillaumot, P. 122 199 Anis, Y., see Bubis, M. 123 139 Bendena, W.G., see Vanden Broeck, J. 122 191 Antoine, M., Gaiddon, C., Loeffler, J.P., Ca** /calmodulin kinase Berger, P., Bidart, J.-M., Delves, P.S., Dirnhofer, S., Hoermann, R.., types II and IV regulate c-fos transcription in the AtT20 corti- Isaacs, N., Jackson, A., Klonisch, T., Lapthorn, A., Lund, T.., cotroph cell line 120 | Mann, K., Roitt, I., Schwarz, S., Wick, G., Immunochemical Aouani, A., see Fayet, G. 117 111 mapping of gonadotropins 125 33 Aoyama, A., see Scheier, B. 123 187 Bergh, J., see Gustavsson, B. 121 143 Apa, R., Caruso, A., Andreani, C.L., Miceli, F., Lazzarin, N., Berka, J.L., Kelly, D.J., Robinson, D.B., Alcorn, D., Marley, P.D., Mastrandrea, M., Ronsisvalle, E., Mancuso, S., Lanzone, A., Fernley, R.T., Skinner, S.L., Adrenaline cells of the rat adrenal Growth hormone stimulates androsterone synthesis by rat theca-in- cortex and medulla contain renin and prorenin 119 175 terstitial cells 118 95 Bernard, M.P., see Han, Y. 124 151 Appel, D.A., see Stadelmann, A.M. 116 31 Berndtson, A.K., Weaver, C.J., Fortune, J.E., Differential effects of Aptel, H., Johnson, E.I.M., Vallotton, M.B., Rossier, M.F., Capponi, oxytocin on steroid production by bovine granulosa cells 116 191 A.M., Demonstration of an angiotensin II-induced negative feed- Bernhardt, R., see Denner, K. 121 87 back effect on aldosterone synthesis in isolated rat adrenal zona Bertoglio, J., see Cussac, D. 119 195 glomerulosa cells 119 105 Bhowmick, N., see Puett, D. 125 55 Arnold, S.F., Klotz, D.M., Vonier, P.M., Collins, B.M., McLachlan, Bidart, J.-M., see Berger, P. 125 33 J.A., Synergism in estrogen-regulated gene expression 123 119 Bidart, J.-M., see Remy, J.-J. 125 79 Arora, K., see Scaldaferri, L. 117 227 Bignon, C., see Daniel, N. 118 25 Arzt, E., see Pereda, M.P. 124 33 Billiard, J., Functional heterogeneity of pituitary gonadotropes in Ashcroft, S.J.H., see Tian, Y.-M. 119 185 response to a variety of neuromodulators 123 163 Auersperg, N., see Lie, B.-L. 120 169 Bird, I.M., see Denner, K. 121 87 Autelitano, D.J., Cohen, D.R., CRF stimulates expression of multiple Birken, S., Kovalevskaya, G., O'Connor, J., Metabolism of hCG and fos and jun related genes in the AtT-20 corticotroph cell 119 25 hLH to multiple urinary forms 125 121 234 Cumulative author index vols. 116—125 (1997) Bjurulf, E., see Olofsson, J.1. 123 45 Canfield, R.E., see Lustbader, J.W. 125 21 Blais, Y.. Gingras, S., Haagensen, D.E., Labrie, F., Simard, J., Capone, J.P., see Hunter, J. 116 213 Interleukin-4 and interleukin-13 inhibit estrogen-induced breast Capone, J.P., see Marcus, S.L. 120 31 cancer cell proliferation and stimulate GCDFP-1I5 expression in Capponi, A.M., see Aptel, H. 119 105 human breast cancer cells 121 11 Carrizo, G., see Pereda, M.P. 124 33 Bodart, V., Rainey, W.E., Fournier, A., Ong, H., De Léan, A., The Carter, D., see Smith, M. 122 151 H295R human adrenocortical cell line contains functional atrial Carter, D.A., Murphy, D., Circadian rhythms and autoregulatory natriuretic peptide receptors that inhibit aldosterone biosynthesis transcription loops going round in circles? 124 | 118 137 Caruso, A., see Apa, R. 118 95 Boddy, S., see Jabbour, H.N. 123 17 Casteilla, L., see Reyne, Y. 116 59 Boen, E.A., see Kepa, J.K. 117 27 Castelein, H., Janssen, A., Declercq, P.E., Baes, M., Sequence re- Boeuf, G., see Elies, G. 124 131 quirements for high affinity retinoid X receptor-x homodimer Boime, I., see Sugahara, T. 125 71 binding 119 11 Boland, R., see Morelli, S. 122 207 Cato, A.C.B., see Neuschmid-Kaspar, F. 117 149 Boland, R., see Picotto, G. 119 129 Catt, K.J., see Scaldaferri, L. 117 227 Bona, C.A., see Shang Wang, B. 116 223 Cattini, P.A., see Lytras, A. 119 1 Borboni, P., Porzio, O., Magnaterra, R., Fusco, A., Sesti, G., Lauro, Cattini, P.A., see Nickel, B.E. 118 155 R., Marlier, L.N.J.L., Quantitative analysis of pancreatic glucoki- Caussanel, V., Tabone, E., Mauduit, C., Dacheux, F., Benahmed, M.., nase gene expression in cultured /cells by competitive polymerase Cellular distribution of EGF, TGF and their receptor during chain reaction 117 175 postnatal development and spermatogenesis of the boar testis 123 Bottari, S.P., see Meffert, S. 122 59 61 Bouchard, P., see Christin-Maitre, S. 125 151 Cetani, F., see Van Sande, J. 119 161 Boujard, D., see Elies, G. 124 131 Chabaud, O., see Desruisseau, S. 122 223 Bousfield, G.R., Butnev, V.Y., Gotschall, R.R., Baker, V.L., Moore, Chandorkar, A., see Gupta, C. 123 89 W.T., Structural features of mammalian gonadotropins 125 3 Chang, A.C.-M., see Nelson, A.E. 124 17 Boyd, R.T., see Enyeart, J.J. 124 97 Chang, A.C.-M., Dunham, M.A., Jeffrey, K.J., Reddel, R.R., Molec- Bozon, V., see Remy, J.-J. 125 79 ular cloning and characterization of mouse stanniocalcin cDNA Brachet, P., see Jehan, F. 116 149 124 185 Brandt, M., see Krogh Rasmussen, A. 116 173 Chang, E.Y., see Paquet, L. 120 161 Brandt, M., see Rasmussen, A.K. 116 165 Chang, L., see Ryu, K.-S. 125 93 Braulke, T., see K6rner, C. 118 201 Chatelain, N., see de Roux, N. 117 253 Breier, B.H., see Butler, A.A. 116 181 Chen, C.-W., Roy, D., Up-regulation of nuclear IGF-I receptor by Briand, P., see Lundholt, B.K. 119 47 short term exposure of stilbene estrogen, diethylstilbestrol 118 | Broadway, D.E., see Wilden, P.A. 122 131 Chen, Z.-G., see Dong, K.-W. 117 241 Brochu, M., see Forcier, I]. 117 189 Cheng, K.-W., see Dong, K.-W. 117 241 Brown, J.M., see Lustbader, J.W. 125 21 Chervin, A.. see Pereda, M.P. 124 33 Brown, T.R., see Mare Lobaccaro, J. 116 137 Cheung, T.C., see Nolan, E.M. 124 51 Bubis, M., Anis, Y., Zisapel, N., Enhancement by melatonin of GTP Chiche, L., see Mare Lobaccaro, J. 116 137 exchange and ADP ribosylation reactions 123 139 Choi, W.S., see Lee, B.J. 118 9 Buckingham, D.W., see Aitken, R.J. 117 83 Chow, Y.-S., see Gu, S.-H. 120 99 Budnik, L.T., Mukhopadhyay, A.K., Modulatory action of epider- Christin-Maitre, S., Bouchard, P., Bioassays of gonadotropins based mal growth factor on differentiated human granulosa lutein cells: on cloned receptors 125 151 cross-talk between ligand activated receptors for EGF and go- Chung, C.S., see Song, S. 120 193 nadotropin 124 141 Chung, H.-O., Kato, T., Kato, Y., Molecular cloning of c-jun and Bulun, S.E., see Crichton, M.B. 118 217 c-fos cDNAs from porcine anterior pituitary and their involvement Bunting, R., see Reid, G. 124 121 in gonadotropin-releasing hormone stimulation 119 75 Burgon, P.G., see Stanton, P.G. 125 133 Claessens, F., see Vanaken, H. 121 197 Burke, Z., see Smith, M. 122 151 Clarke, L.A., see Jabbour, H.N. 123 17 Burlingame, S., see Jetten, A.M. 123 7 Clawson, T.F., Lee, W.-H., Yoder, M.C., Differential expression of Burton, D.W., see Nolan, E.M. 124 51 insulin-like growth factor binding proteins in murine hematopoietic Butkus, A., see Roche, P.J. 121 171 stromal cell lines 120 59 Butler, A.A., Funk, B., Breier, B.H., LeRoith, D., Roberts Jr., C.T., Cohen, D.R., see Autelitano, D.J. 119 25 Gluckman, P.D., Growth hormone (GH) status regulates GH Cohen, H., see Prigent-Tessier, A. 122 101 receptor and GH binding protein mRNA in a tissue- and tran- Cobick,C:B., Daa. G., Xu; \L.,, Deb;'S:,. Kamei. T,. Levan. ‘G:, script-specific manner but has no effect on insulin-like growth Szpirer, C., Szpirer, J.. Kwok, S.C.M., Soares, M.J., Placental factor-I receptor mRNA in the rat 116 181 lactogen-I variant utilizes the prolactin receptor signaling pathway Butnev, V.Y., see Bousfield, G.R. 125 3 116 49 Borglum, J.D., Vassaux, G., Richelsen, B., Gaillard, D., Darimont, Colas, B., see Marinero, M.J. 118 193 C., Ailhaud, G., Négrel, R., Changes in adenosine A,- and A,-re- Collins, B.J., Szabo, M., Cuttler, L., Differential desensitization ceptor expression during adipose cell differentiation 117 17 response of the neonatal and adult rat somatotroph to growth hormone-releasing hormone and phorbol ester 117 75 Calvo, R., see Solé, E. 119 147 Collins, B.M., see Arnold, S.F. 123 119 Cambon, B., see Reyne, Y. 116 59 Contempre, B., Le Moine, O., Dumont, J.E., Denef, J.-F.. Many, Campbell, L.E., Yu, M., Yang, K., Ovine 11/-hydroxysteroid dehy- M.C., Selenium deficiency and thyroid fibrosis. A key role for drogenase type 2 gene predicts a protein distinct from that deduced macrophages and transforming growth factor #/(TGF-f) 124 7 by the cloned kidney cDNA at the C-terminus 119 113 Cool, D.R., see Friedman, T.C. 116 89

See more

The list of books you might like

Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.