-
2
-
-
0023849563
-
Steroid receptor-mediated inhibition of rat prolactin gene expression does require the receptor DNA-binding domain
-
ADLER S, WATERMAN ML, HE X, ROSENFELD MG. Steroid receptor-mediated inhibition of rat prolactin gene expression does require the receptor DNA-binding domain Cell 1988 ; 52 : 685-95
-
(1988)
Cell
, vol.52
, pp. 685-695
-
-
Adler, S.1
Waterman, M.L.2
He, X.3
Rosenfeld, M.G.4
-
3
-
-
0018384017
-
Multiple pituitary hormone deficiences in eight siblings of one Jewish moroccan family
-
ADLER-BIER M, PERTZELAN A, LARON Z, LIEBERMAN E, MOSES S. Multiple pituitary hormone deficiences in eight siblings of one Jewish moroccan family. Acta Paediatr Scand 1979 ; 68 : 401-4.
-
(1979)
Acta Paediatr Scand
, vol.68
, pp. 401-404
-
-
Adler-Bier, M.1
Pertzelan, A.2
Laron, Z.3
Lieberman, E.4
Moses, S.5
-
5
-
-
0029608970
-
The Ames dwarf gene is required for Pit-I gene activation
-
ANDERSEN B, PEARSE RV, JENNE K et al. The Ames dwarf gene is required for Pit-I gene activation. Dev Biol 1995 ; 172 : 495-503.
-
(1995)
Dev Biol
, vol.172
, pp. 495-503
-
-
Andersen, B.1
Pearse, R.V.2
Jenne, K.3
-
6
-
-
0028126819
-
Pit-I determines cell types during development of the anterior pituitary gland. A model for transcriptional regulation of cell phenotypes in mammalian organogenesis
-
ANDERSEN B, ROSENFELD MG. Pit-I determines cell types during development of the anterior pituitary gland. A model for transcriptional regulation of cell phenotypes in mammalian organogenesis. J Biol Chem 1994 ; 269 29335-8.
-
(1994)
J Biol Chem
, vol.269
, pp. 29335-29338
-
-
Andersen, B.1
Rosenfeld, M.G.2
-
7
-
-
0026519203
-
Magnetic resonance imaging in the diagnosis of growth hormone deficiency
-
ARGYROPOLLOL M, PERIGNON F, BRAUNER R, BRUNELLE F Magnetic resonance imaging in the diagnosis of growth hormone deficiency. J Pediatr 1992 ; 120 : 886-91
-
(1992)
J Pediatr
, vol.120
, pp. 886-891
-
-
Argyropollol, M.1
Perignon, F.2
Brauner, R.3
Brunelle, F.4
-
9
-
-
0003075917
-
The hypothalamic-pituitary axis
-
Melmed S Black-well Science
-
ASA SL, KOVACS K, MELMED S. The hypothalamic-pituitary axis. In : The Pituitary Melmed S Black-well Science 1995 ; 3-44
-
(1995)
The Pituitary
, pp. 3-44
-
-
Asa, S.L.1
Kovacs, K.2
Melmed, S.3
-
10
-
-
0025302088
-
Growth hormone treatment in the United States : Demographic and diagnostic features of 2331 children
-
AUGUST GP, LIPPE BM, BLETHEN SL et al. Growth hormone treatment in the United States : demographic and diagnostic features of 2331 children. J Pediatr 1990 ; 116 : 899-903.
-
(1990)
J Pediatr
, vol.116
, pp. 899-903
-
-
August, G.P.1
Lippe, B.M.2
Blethen, S.L.3
-
11
-
-
0028965157
-
P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell committment and synergizes with Pit-1
-
BACH I, RHODES SJ, PEARSE RV et al. P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell committment and synergizes with Pit-1. Proc Natl Acad Sci USA 1995 ; 92 : 2720-4
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 2720-2724
-
-
Bach, I.1
Rhodes, S.J.2
Pearse, R.V.3
-
12
-
-
0024277966
-
The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein
-
BODNER M, CASTRILLO J-L, THEILL LE et al. The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein. Cell 1988 ; 55 : 505-18.
-
(1988)
Cell
, vol.55
, pp. 505-518
-
-
Bodner, M.1
Castrillo, J.-L.2
Theill, L.E.3
-
13
-
-
0000360419
-
An evaluation of seventy-five patients with hypopituitarism beginning in childhood
-
BRASEL JA, WRIGHT JC, WILKINS L, BLIZZARD RM. An evaluation of seventy-five patients with hypopituitarism beginning in childhood. Am J Med 1965 , 38 : 484-98
-
(1965)
Am J Med
, vol.38
, pp. 484-498
-
-
Brasel, J.A.1
Wright, J.C.2
Wilkins, L.3
Blizzard, R.M.4
-
15
-
-
0345342684
-
Genetic polymorphism in combined pituitary hormone deficiency
-
Stockholm
-
BRUE T, JORGENSEN JOL, SANDAHI J et al Genetic polymorphism in combined pituitary hormone deficiency. ESPE meeting. Stockholm, 1997.
-
(1997)
ESPE Meeting
-
-
Brue, T.1
Jorgensen, J.O.L.2
Sandahi, J.3
-
16
-
-
0029694433
-
The gene responsible tor adrenal hypoplasia congenita, DAX-I, encodes a nuclear hormone receptor that defines a new class within the superfamily
-
BURRIS TP, GUO W. E.R. M. The gene responsible tor adrenal hypoplasia congenita, DAX-I, encodes a nuclear hormone receptor that defines a new class within the superfamily. Rec Prog Horm Res 1996 ; 51 . 241-59.
-
(1996)
Rec Prog Horm Res
, vol.51
, pp. 241-259
-
-
Burris, T.P.1
Guo, W.E.R.M.2
-
17
-
-
0028825415
-
Isolated growth hormone deficiency . testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor
-
CAO Y, WAGNER JK, HINDMARSH PC, EBLE A, MULLIS PE. Isolated growth hormone deficiency . testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor. Ped Res 1995 , 38 . 962-6.
-
(1995)
Ped Res
, vol.38
, pp. 962-966
-
-
Cao, Y.1
Wagner, J.K.2
Hindmarsh, P.C.3
Eble, A.4
Mullis, P.E.5
-
18
-
-
0025277540
-
Autoregulation of Pit-I gene expression mediated by two cis-active promoter elements
-
CHEN R, INGRAHAM HA, TREACY MN et al. Autoregulation of Pit-I gene expression mediated by two cis-active promoter elements. Nature 1990; 346 : 583-6.
-
(1990)
Nature
, vol.346
, pp. 583-586
-
-
Chen, R.1
Ingraham, H.A.2
Treacy, M.N.3
-
19
-
-
0028827048
-
Imperforate anus, bilateral hydronephrosis. bilateral undescended testes and pituitary hypoplasia : A variant of Hall-Pallister syndrome or a new syndrome ?
-
CIANTARANI S, VITALE S, STANHOPE R, BOSCHERINI B. Imperforate anus, bilateral hydronephrosis. bilateral undescended testes and pituitary hypoplasia : a variant of Hall-Pallister syndrome or a new syndrome ? Acta Paediatr 1995 ; 84 . 1322-4.
-
(1995)
Acta Paediatr
, vol.84
, pp. 1322-1324
-
-
Ciantarani, S.1
Vitale, S.2
Stanhope, R.3
Boscherini, B.4
-
20
-
-
0028129676
-
Molecular insights into inherited ACTH resistance syndromes
-
CLARK AJL, WEBER A. Molecular insights into inherited ACTH resistance syndromes. Trends Endocrinol Metab 1994 ; 5 : 209-14.
-
(1994)
Trends Endocrinol Metab
, vol.5
, pp. 209-214
-
-
Clark, A.J.L.1
Weber, A.2
-
21
-
-
0344480069
-
A novel mutation in the phosphorylation consensus sequence if the Pit-1 gene in a patient with dysregulation of prolactin and thyrotropin secretion
-
COHEN LE, WONDISFORD FE, RADOVICK S A novel mutation in the phosphorylation consensus sequence if the Pit-1 gene in a patient with dysregulation of prolactin and thyrotropin secretion. Prog 76th Meeting of the Endocrine Soc 1994 ; 6 : 202.
-
(1994)
Prog 76th Meeting of the Endocrine Soc
, vol.6
, pp. 202
-
-
Cohen, L.E.1
Wondisford, F.E.2
Radovick, S.3
-
22
-
-
0029835520
-
Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin
-
COHEN LE, WONDISFORD FE, RADOVICK S. Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin. Endocrinol Metab Clin North Am 1996 ; 25 : 523-40.
-
(1996)
Endocrinol Metab Clin North Am
, vol.25
, pp. 523-540
-
-
Cohen, L.E.1
Wondisford, F.E.2
Radovick, S.3
-
23
-
-
0028980503
-
A « hot spot »in the Pit-1 gene responsable for combined pituitary hormone deficiency . clinical and molecular correlates
-
COHEN LE, WONDISFORD FE, SALVATONI A et al. A « hot spot »in the Pit-1 gene responsable for combined pituitary hormone deficiency . clinical and molecular correlates. J Clin Endocrinol Metab 1995 , 80 : 679-84.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 679-684
-
-
Cohen, L.E.1
Wondisford, F.E.2
Salvatoni, A.3
-
24
-
-
0022391052
-
Mapping of the early neural primordium in quail-chick chimeras. I-Developmental relationships between placodes, facial ectoderm, and prosencephalon
-
COULY GF, LE DOUARIN NM. Mapping of the early neural primordium in quail-chick chimeras. I-Developmental relationships between placodes, facial ectoderm, and prosencephalon. Dev Biol 1985 ; 110 : 422-39.
-
(1985)
Dev Biol
, vol.110
, pp. 422-439
-
-
Couly, G.F.1
Le Douarin, N.M.2
-
25
-
-
0024515809
-
Induction of human growth hormone promoter activity by the adenosine 3′, 5′ - Monophosphate pathway involves a novel responsive element
-
DANA S, KARIN M. Induction of human growth hormone promoter activity by the adenosine 3′, 5′ - monophosphate pathway involves a novel responsive element. Mol Endocrinol 1989 ; 3 : 815-21.
-
(1989)
Mol Endocrinol
, vol.3
, pp. 815-821
-
-
Dana, S.1
Karin, M.2
-
26
-
-
0028865778
-
A prismatic case. The prenatal role of thyroid hormone evidenced by fetomaternal Pit-I deficiency
-
DE ZEGHER F, PERNASETTI F, VANHOLE C et al. A prismatic case. The prenatal role of thyroid hormone evidenced by fetomaternal Pit-I deficiency. J Clin Endocrinol Metab 1995 ; 80 : 3127-30.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 3127-3130
-
-
De Zegher, F.1
Pernasetti, F.2
Vanhole, C.3
-
27
-
-
0026091281
-
TEF, a transcription factor expressed specifically in the anterior pituitary during embryogenesis, defines a new class of leucine zipper proteins
-
DROLET DW, SCULLY KM, SIMMONS DM et al TEF, a transcription factor expressed specifically in the anterior pituitary during embryogenesis, defines a new class of leucine zipper proteins. Genes Dev 1991 ; 5 : 1739-53.
-
(1991)
Genes Dev
, vol.5
, pp. 1739-1753
-
-
Drolet, D.W.1
Scully, K.M.2
Simmons, D.M.3
-
28
-
-
0026340910
-
Inhibitory control of prolactin and Pit-I gene promoters by dopamine
-
ELSHOLTZ HP, LEW AM, ALBERT PR, SUNDMARK VC. Inhibitory control of prolactin and Pit-I gene promoters by dopamine. J Biol Chem 1991 ; 266 : 22919-25.
-
(1991)
J Biol Chem
, vol.266
, pp. 22919-22925
-
-
Elsholtz, H.P.1
Lew, A.M.2
Albert, P.R.3
Sundmark, V.C.4
-
29
-
-
0025938481
-
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
-
FRANCO B, GUIOLI S, PRAGLIOLA A. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature 1991 ; 353 : 529-36.
-
(1991)
Nature
, vol.353
, pp. 529-536
-
-
Franco, B.1
Guioli, S.2
Pragliola, A.3
-
30
-
-
0029908916
-
The Armes dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation
-
GAGE PJ, BRINKMEIER ML, SCARLETT LM et al. The Armes dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation Mol Endocrinol 1996 , 10 : 1570-81.
-
(1996)
Mol Endocrinol
, vol.10
, pp. 1570-1581
-
-
Gage, P.J.1
Brinkmeier, M.L.2
Scarlett, L.M.3
-
31
-
-
0020614294
-
Prolactin and thyrotropin responses to thyroliberin (TRH) in patients with growth hormone deficiency : Study in 167 patients
-
GARNIER PE, ROGER M, CHAUSSAIN JL, CANLORBE P, JOB JC. Prolactin and thyrotropin responses to thyroliberin (TRH) in patients with growth hormone deficiency : study in 167 patients. Acta Endocrinol (Copenh) 1983 , 103 : 433-40.
-
(1983)
Acta Endocrinol (Copenh)
, vol.103
, pp. 433-440
-
-
Garnier, P.E.1
Roger, M.2
Chaussain, J.L.3
Canlorbe, P.4
Job, J.C.5
-
32
-
-
0027265595
-
GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor function
-
GODFREY P, RAHAL JO, BEAMER WG et al. GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor function. Nature Genet 1993 ; 4 : 227-32
-
(1993)
Nature Genet
, vol.4
, pp. 227-232
-
-
Godfrey, P.1
Rahal, J.O.2
Beamer, W.G.3
-
33
-
-
0014410431
-
Growth and growth hormone. II - A comparison of isolated growth-hormone deficiency and multiple pituitary hormone deficiency in 35 patients with idiopathic hypopituitary dwarfism
-
GOODMAN HG, GRUMBACH MM, KAPLAN SL, Growth and growth hormone. II - A comparison of isolated growth-hormone deficiency and multiple pituitary hormone deficiency in 35 patients with idiopathic hypopituitary dwarfism. N Engl J Med 1968 ; 278 : 57-68.
-
(1968)
N Engl J Med
, vol.278
, pp. 57-68
-
-
Goodman, H.G.1
Grumbach, M.M.2
Kaplan, S.L.3
-
34
-
-
0029809471
-
Adrenal hypoplasia congenita with hypogonadotropic hypogonadism. Evidence that Dax-1 mutations lead to combined hypothalamic and hypopituitary defects in gonadotropin production
-
HABIBY RL, BOEPPLE P, NACHTIGALL L et al. Adrenal hypoplasia congenita with hypogonadotropic hypogonadism. Evidence that Dax-1 mutations lead to combined hypothalamic and hypopituitary defects in gonadotropin production. J Clin Invest 1996 ; 98 : 1055-62.
-
(1996)
J Clin Invest
, vol.98
, pp. 1055-1062
-
-
Habiby, R.L.1
Boepple, P.2
Nachtigall, L.3
-
36
-
-
0028938891
-
Transcription factor Pit-1 and its clinical implications : From bench to bedside
-
HAUGEN BR, RIDGWAY EC. Transcription factor Pit-1 and its clinical implications : from bench to bedside. Endocrinologist 1995 ; 5 : 132-9
-
(1995)
Endocrinologist
, vol.5
, pp. 132-139
-
-
Haugen, B.R.1
Ridgway, E.C.2
-
37
-
-
0027385347
-
A thyrotrope-specific variant of Pit-1 transactivates the thyrotropin beta promoter
-
HAUGEN BR, WOOD WM, GORDON DF. A thyrotrope-specific variant of Pit-1 transactivates the thyrotropin beta promoter. J Biol Chem 1993 ; 268 : 20818-24.
-
(1993)
J Biol Chem
, vol.268
, pp. 20818-20824
-
-
Haugen, B.R.1
Wood, W.M.2
Gordon, D.F.3
-
38
-
-
0025861903
-
Mechanisms of complex transcriptional regulation : Implications for brain development
-
HE X, ROSENDELD MG. Mechanisms of complex transcriptional regulation : implications for brain development. Neuron 1991 , 7 : 183-6.
-
(1991)
Neuron
, vol.7
, pp. 183-186
-
-
He, X.1
Rosendeld, M.G.2
-
39
-
-
0030068242
-
Rpx : A novel anterior-restricted homeobox gene progressively activated in the prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo
-
HERMESZ E, MACKEM S, MAHON KA. Rpx : a novel anterior-restricted homeobox gene progressively activated in the prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo. Development 1996 ; 122 : 41-52.
-
(1996)
Development
, vol.122
, pp. 41-52
-
-
Hermesz, E.1
Mackem, S.2
Mahon, K.A.3
-
40
-
-
0025272043
-
A family of POU-domain and Pit-1 tissue-specific transcription factors in pituitary and neuroendocrine development
-
INGRAHAM HA, ALBERT VR, CHEN R et al. A family of POU-domain and Pit-1 tissue-specific transcription factors in pituitary and neuroendocrine development. Ann Rev Physiol 1990 ; 52 : 773-91.
-
(1990)
Ann Rev Physiol
, vol.52
, pp. 773-791
-
-
Ingraham, H.A.1
Albert, V.R.2
Chen, R.3
-
41
-
-
0024277940
-
A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype
-
INGRAHAM HA, CHEN R, MANGALAM HJ et al. A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype. Cell 1988 ; 55 : 519-29.
-
(1988)
Cell
, vol.55
, pp. 519-529
-
-
Ingraham, H.A.1
Chen, R.2
Mangalam, H.J.3
-
42
-
-
0025339078
-
The POU-specific domain of Pit-1 is essential for sequence-specific, high affinity DNA binding and DNA-dependent Pit-1-Pit-1 interactions
-
INGRAHAM HA, FLYNN SE, Voss JW et al. The POU-specific domain of Pit-1 is essential for sequence-specific, high affinity DNA binding and DNA-dependent Pit-1-Pit-1 interactions. Cell 1990 , 61 : 1021-33.
-
(1990)
Cell
, vol.61
, pp. 1021-1033
-
-
Ingraham, H.A.1
Flynn, S.E.2
Voss, J.W.3
-
43
-
-
0029014128
-
Screening for Pit-1 abnormality by PCR direct sequencing method
-
IRIE Y, TATSUMI KI, KUSUDA S et al. Screening for Pit-1 abnormality by PCR direct sequencing method Thyroid 1995 ; 5 : 207-11.
-
(1995)
Thyroid
, vol.5
, pp. 207-211
-
-
Irie, Y.1
Tatsumi, K.I.2
Kusuda, S.3
-
44
-
-
0029121819
-
A novel E250X mutation of the Pit-I gene is a patient with combined pituitary hormone deficiency
-
IRIE Y, TATSUMI KI, OGAWA M et al. A novel E250X mutation of the Pit-I gene is a patient with combined pituitary hormone deficiency. Endocrine J 1995 ; 42 : 351-4
-
(1995)
Endocrine J
, vol.42
, pp. 351-354
-
-
Irie, Y.1
Tatsumi, K.I.2
Ogawa, M.3
-
45
-
-
0031020234
-
DAX-1 inhibits SF-1 mediated transactivation via a carboxy-terminal domain that is deleted in adrenal hypoplasia congenita
-
ITO M, Yu R, JAMESON JL. DAX-1 inhibits SF-1 mediated transactivation via a carboxy-terminal domain that is deleted in adrenal hypoplasia congenita. Mol Cell Biol 1997 ; 17 : 1476-783.
-
(1997)
Mol Cell Biol
, vol.17
, pp. 1476-1783
-
-
Ito, M.1
Yu, R.2
Jameson, J.L.3
-
46
-
-
0031057121
-
Structure of Pit-1 POU domain bound to DNA as a dimer . unexpected arrangement and flexibility
-
JACOBSON EM, LI P, LEON-DEL-RIO A, ROSENFELD MG, AGGARWAL AK. Structure of Pit-1 POU domain bound to DNA as a dimer . unexpected arrangement and flexibility. Dev Biol 1997 ; 11 : 198-212.
-
(1997)
Dev Biol
, vol.11
, pp. 198-212
-
-
Jacobson, E.M.1
Li, P.2
Leon-Del-Rio, A.3
Rosenfeld, M.G.4
Aggarwal, A.K.5
-
47
-
-
0029868645
-
Crystallization and preliminary X-ray analysis of Pit-1 POU domain complexed to a 28 base pair DNA element
-
JACOBSON EM, Li P, ROSENFELD, AGGARWAL AK. Crystallization and preliminary X-ray analysis of Pit-1 POU domain complexed to a 28 base pair DNA element. Proteins 1996 , 24 : 263-5
-
(1996)
Proteins
, vol.24
, pp. 263-265
-
-
Jacobson, E.M.1
Li, P.2
Rosenfeld3
Aggarwal, A.K.4
-
48
-
-
0030057596
-
The T/ebp null mouse : Thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid. lung. ventral forebrain, and pituitary
-
KIMURA S, HARA Y, PINEAU T et al. The T/ebp null mouse : thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid. lung. ventral forebrain, and pituitary. Genes Dev 1996 ; 10 60-9.
-
(1996)
Genes Dev
, vol.10
, pp. 60-69
-
-
Kimura, S.1
Hara, Y.2
Pineau, T.3
-
49
-
-
0019725944
-
Primary empty sella and Rieger's anomaly of the anterior chamber of the eye : A familial syndrome
-
KLEINMANN KE, KAZARIAN EL, RAPTOPOULOS V, BRANERMAN LE. Primary empty sella and Rieger's anomaly of the anterior chamber of the eye : a familial syndrome. N Engl J Med 1981 ; 304 : 90-3.
-
(1981)
N Engl J Med
, vol.304
, pp. 90-93
-
-
Kleinmann, K.E.1
Kazarian, E.L.2
Raptopoulos, V.3
Branerman, L.E.4
-
50
-
-
0028200262
-
Crystal structure of the Oct-1 POU domain bound to an octamer site : DNA recognition with tethered DNA-binding modules
-
KLEMM JD, ROULD MA, AURORA R, HERR W, PABO Co. Crystal structure of the Oct-1 POU domain bound to an octamer site : DNA recognition with tethered DNA-binding modules. Cell 1994 ; 77 : 21-32.
-
(1994)
Cell
, vol.77
, pp. 21-32
-
-
Klemm, J.D.1
Rould, M.A.2
Aurora, R.3
Herr, W.4
Pabo, Co.5
-
51
-
-
0004473106
-
Transcription factors and endocrine diseases
-
KULIG E. R.V.L. Transcription factors and endocrine diseases. Endocr Pathol 1996 ; 7 : 245-50.
-
(1996)
Endocr Pathol
, vol.7
, pp. 245-250
-
-
Kulig, E.R.V.L.1
-
52
-
-
0030568155
-
Transcription-factors mutations and disease
-
LAICHMAN DS. Transcription-factors mutations and disease. N Engl J Med 1996 ; 334 : 28-33
-
(1996)
N Engl J Med
, vol.334
, pp. 28-33
-
-
Laichman, D.S.1
-
53
-
-
0029812609
-
Luteinizing hormone deficiency and female infertility in mice lacking the transcription factor NGFI-A (Egr-1)
-
LEE SL, SADOVSKY Y, SWIRNOFF AH et al. Luteinizing hormone deficiency and female infertility in mice lacking the transcription factor NGFI-A (Egr-1) Science 1996, 27 : 1219-21.
-
(1996)
Science
, vol.27
, pp. 1219-1221
-
-
Lee, S.L.1
Sadovsky, Y.2
Swirnoff, A.H.3
-
54
-
-
0025940669
-
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
-
LEGOUIS L, HARDELIN JP, LEVILLIERS J The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules. Cell 1991 ; 67 : 423-35
-
(1991)
Cell
, vol.67
, pp. 423-435
-
-
Legouis, L.1
Hardelin, J.P.2
Levilliers, J.3
-
55
-
-
0025014024
-
Dwarf locus mutants lacking three pituitary cell types from mutations in the POU-domain gene pit-I
-
Li S, CRENSHAW EB, RAWSON EJ et al. Dwarf locus mutants lacking three pituitary cell types from mutations in the POU-domain gene pit-I. Nature 1990 ; 347 . 528-32.
-
(1990)
Nature
, vol.347
, pp. 528-532
-
-
Li, S.1
Crenshaw, E.B.2
Rawson, E.J.3
-
56
-
-
0028793120
-
In vivo mutational analysis of the DNA binding domain of the tissue-specific transcription factor Pit-1
-
LIAXG J, MOYE-ROWLEY S, MAURER RA. In vivo mutational analysis of the DNA binding domain of the tissue-specific transcription factor Pit-1. J Biol Chem 1995 ; 270 : 25520-5.
-
(1995)
J Biol Chem
, vol.270
, pp. 25520-25525
-
-
Liaxg, J.1
Moye-Rowley, S.2
Maurer, R.A.3
-
57
-
-
0027076516
-
Pit-dependent expression of the receptor for growth hormone releasing factor mediates pituitary cell growth
-
LIN C, LIN S-C, CHANG C-P, ROSENFELD MG. Pit-dependent expression of the receptor for growth hormone releasing factor mediates pituitary cell growth. Nature 1992 ; 360 : 765-8
-
(1992)
Nature
, vol.360
, pp. 765-768
-
-
Lin, C.1
Lin, S.-C.2
Chang, C.-P.3
Rosenfeld, M.G.4
-
58
-
-
0028345604
-
Pituitary ontogeny of the Snell dwarf mouse reveals Pit-1-independent and Pit-1-dependent origins of the thyrotrope
-
LIN S-C, LI S, DROLET DW, ROSENFELD MG Pituitary ontogeny of the Snell dwarf mouse reveals Pit-1-independent and Pit-1-dependent origins of the thyrotrope. Development 1994 ; 120 : 515-22
-
(1994)
Development
, vol.120
, pp. 515-522
-
-
Lin, S.-C.1
Li, S.2
Drolet, D.W.3
Rosenfeld, M.G.4
-
59
-
-
0027236844
-
Molecular basis of the little mouse phenotype and implications for cell-type specific growth
-
LIN SC, LIN CR, GUKOVSKY I et al. Molecular basis of the little mouse phenotype and implications for cell-type specific growth. Nature 1993 ; 364 : 208-13.
-
(1993)
Nature
, vol.364
, pp. 208-213
-
-
Lin, S.C.1
Lin, C.R.2
Gukovsky, I.3
-
60
-
-
0028319104
-
Utah growth study : Growth standards and the prevalence of growth hormone deficiency
-
LINDSAY R, FELDKAMP M, HARRIS D. Utah growth study : growth standards and the prevalence of growth hormone deficiency. J Pediatr 1994 ; 125 : 29-35.
-
(1994)
J Pediatr
, vol.125
, pp. 29-35
-
-
Lindsay, R.1
Feldkamp, M.2
Harris, D.3
-
61
-
-
0027257302
-
Identification of a novel zinc finger protein binding a conserved element critical for Pit-1 dependent growth hormone gene expression
-
LIPKIN SM, NAAR AM, KALLA KA Identification of a novel zinc finger protein binding a conserved element critical for Pit-1 dependent growth hormone gene expression. Genes Dev 1993 ; 7 : 1674-87.
-
(1993)
Genes Dev
, vol.7
, pp. 1674-1687
-
-
Lipkin, S.M.1
Naar, A.M.2
Kalla, K.A.3
-
62
-
-
0031567823
-
Targeted mutation in beta1.4-Galactosyltransferase leads to pituitary insufficiency and neonatal lethality
-
LU Q, HASTY P, SHUR BD. Targeted mutation in beta1.4-Galactosyltransferase leads to pituitary insufficiency and neonatal lethality. Dev Biol 1997 ; 181 . 257-67.
-
(1997)
Dev Biol
, vol.181
, pp. 257-267
-
-
Lu, Q.1
Hasty, P.2
Shur, B.D.3
-
63
-
-
0025879961
-
Hypothalamic-pituitary dysfunction in growth-hormone deficient patients with pituitary abnormalities
-
MAGHNIE M, TRIULZI F, LARIZZA D et al. Hypothalamic-pituitary dysfunction in growth-hormone deficient patients with pituitary abnormalities. J Clin Endocrinol Metab 1991 ; 73 : 79-83.
-
(1991)
J Clin Endocrinol Metab
, vol.73
, pp. 79-83
-
-
Maghnie, M.1
Triulzi, F.2
Larizza, D.3
-
65
-
-
0023023132
-
A deletion truncating the gonadotropin-releasing hormone gene is responsible for hypogonadism in the hpg mouse
-
MASON AJ, HAYFLICK JS, ZOELLER T. A deletion truncating the gonadotropin-releasing hormone gene is responsible for hypogonadism in the hpg mouse. Science 1986 ; 234 : 1366-71.
-
(1986)
Science
, vol.234
, pp. 1366-1371
-
-
Mason, A.J.1
Hayflick, J.S.2
Zoeller, T.3
-
66
-
-
0026803163
-
Molecular cloning and expression of a pituitary-specific receptor for growth hormone-releasing hormone
-
MAYO KE. Molecular cloning and expression of a pituitary-specific receptor for growth hormone-releasing hormone. Mol Endocrinol 1992 ; 6 : 1734-44.
-
(1992)
Mol Endocrinol
, vol.6
, pp. 1734-1744
-
-
Mayo, K.E.1
-
67
-
-
0022354210
-
The natural history of familtal hypopituitarism
-
MCARTHUR RG, MORGAN K, PHILLIPS JA, BALA M, KLASSEN J. The natural history of familtal hypopituitarism. Am J med Genest 1985 ; 2 : 553-66.
-
(1985)
Am J Med Genest
, vol.2
, pp. 553-566
-
-
Mcarthur, R.G.1
Morgan, K.2
Phillips, J.A.3
Bala, M.4
Klassen, J.5
-
68
-
-
0025322841
-
Regulation of pituitary-specific homeobox gene GHF-1 by cell-autonomous and environmental cues
-
McCORMICK A, BRADY H, THEIL LE, KARIN M. Regulation of pituitary-specific homeobox gene GHF-1 by cell-autonomous and environmental cues. Nature 1990 ; 345 : 829-32.
-
(1990)
Nature
, vol.345
, pp. 829-832
-
-
McCormick, A.1
Brady, H.2
Theil, L.E.3
Karin, M.4
-
69
-
-
6844248083
-
Familial panhypopituitarism in a consa guineous family from Brazil : A novel type of genetic defect
-
San Francisco
-
MEDEIROS-NETO G, NOGUEIRA C, LEITE CK, CHEDID E, LIBERMAN B. Familial panhypopituitarism in a consa guineous family from Brazil : a novel type of genetic defect. International Congress of Endocrinology, San Francisco, 1996, PI-436 : 243.
-
(1996)
International Congress of Endocrinology
, vol.PI-436
, pp. 243
-
-
Medeiros-Neto, G.1
Nogueira, C.2
Leite, C.K.3
Chedid, E.4
Liberman, B.5
-
70
-
-
0026578988
-
An alternatively spliced Pit-1 isoform altered in its ability to trans-activate
-
MORRIS AE, KLOSS B, McCHESNEY RE, BANCROFT C, CHASIN LA. An alternatively spliced Pit-1 isoform altered in its ability to trans-activate. Nucl Acids Res 1992 ; 20 : 1355-61.
-
(1992)
Nucl Acids Res
, vol.20
, pp. 1355-1361
-
-
Morris, A.E.1
Kloss, B.2
McChesney, R.E.3
Bancroft, C.4
Chasin, L.A.5
-
71
-
-
0030266375
-
Otlx2, an Otx-related homeobox gene expressed in the pituitary gland and in a restricted pattern in the forebrain
-
MUCCHIELLI ML, MARTINEZ S, PATTYN A, GORIDIS C, BRUNET JF. Otlx2, an Otx-related homeobox gene expressed in the pituitary gland and in a restricted pattern in the forebrain. Mol Cell Neurosci 1996 ; 8 : 258-71.
-
(1996)
Mol Cell Neurosci
, vol.8
, pp. 258-271
-
-
Mucchielli, M.L.1
Martinez, S.2
Pattyn, A.3
Goridis, C.4
Brunet, J.F.5
-
72
-
-
0028802965
-
Genetics and molecular biology in short stature
-
MULLIS PE, ARGENTE J, AMSFLEM S, PFAFFLE R, VAN DER BURGT I. Genetics and molecular biology in short stature. Acta Paediatr 1995 ; 411 : 75-80.
-
(1995)
Acta Paediatr
, vol.411
, pp. 75-80
-
-
Mullis, P.E.1
Argente, J.2
Amsflem, S.3
Pfaffle, R.4
Van Der Burgt, I.5
-
73
-
-
0028598360
-
Mutations in the Dax-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
-
MUSCATELLI F, STROM TM, WALKER AP et al. Mutations in the Dax-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature 1994 ; 372 : 672-6.
-
(1994)
Nature
, vol.372
, pp. 672-676
-
-
Muscatelli, F.1
Strom, T.M.2
Walker, A.P.3
-
74
-
-
0023900566
-
Activation of cell-specific expression of rat growth hormone and prolaction genes by a common transcription factor
-
NELSON C, ALBERT VR, ELSHOTZ HP, LU LI-W, ROSENFELD MG. Activation of cell-specific expression of rat growth hormone and prolaction genes by a common transcription factor. Science 1988 ; 239 : 1400-5.
-
(1988)
Science
, vol.239
, pp. 1400-1405
-
-
Nelson, C.1
Albert, V.R.2
Elshotz, H.P.3
Li-W, L.U.4
Rosenfeld, M.G.5
-
75
-
-
0028580550
-
Multiple Pit-1 binding sites facilitate estrogen responsiveness of the prolactin gene
-
NOWAKOWSKI BE, MAURER RA. Multiple Pit-1 binding sites facilitate estrogen responsiveness of the prolactin gene. Mol Endocrinol 1994 ; 8 : 1742-9.
-
(1994)
Mol Endocrinol
, vol.8
, pp. 1742-1749
-
-
Nowakowski, B.E.1
Maurer, R.A.2
-
76
-
-
0027080611
-
Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency
-
OHTA K, NOBUKUNI Y, MITSUBUCHI H et al. Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency. Biochem Biophys Res Comm 1992 ; 189 : 851-5.
-
(1992)
Biochem Biophys Res Comm
, vol.189
, pp. 851-855
-
-
Ohta, K.1
Nobukuni, Y.2
Mitsubuchi, H.3
-
77
-
-
0027980595
-
Monoallelic expression of normal mRNA in the Pit-1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype
-
OKAMOTO N, WADA Y, IDA S et al. Monoallelic expression of normal mRNA in the Pit-1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype. Hum Mol Gen 1994 ; 3 : 1565-8.
-
(1994)
Hum Mol Gen
, vol.3
, pp. 1565-1568
-
-
Okamoto, N.1
Wada, Y.2
Ida, S.3
-
78
-
-
8544242334
-
Null mutation of the prolactin receptor gene produces multiple reproductive defects in the mouse
-
ORMANDY CJ, CAMUS A, BARRA J et al. Null mutation of the prolactin receptor gene produces multiple reproductive defects in the mouse. Genes Dev 1997 ; 11 : 167-78.
-
(1997)
Genes Dev
, vol.11
, pp. 167-178
-
-
Ormandy, C.J.1
Camus, A.2
Barra, J.3
-
79
-
-
0029994991
-
The roles of steroidogenic factor-1 in reproductive function
-
PARKER KL, IKEDA Y, Luo X The roles of steroidogenic factor-1 in reproductive function. Steroids 1996 ; 61 : 161-5.
-
(1996)
Steroids
, vol.61
, pp. 161-165
-
-
Parker, K.L.1
Ikeda, Y.2
Luo, X.3
-
81
-
-
0026919273
-
New genetic findings in old syndromes
-
PARKS JS, PFAFFLE RW, BROWN MR. New genetic findings in old syndromes Acta Paediatr 1992 ; Suppl. 383 : 73-7.
-
(1992)
Acta Paediatr
, vol.383
, Issue.SUPPL.
, pp. 73-77
-
-
Parks, J.S.1
Pfaffle, R.W.2
Brown, M.R.3
-
82
-
-
84995857122
-
Pit-1 gene expression in the human pituitary adenomas
-
PELLEGRINI I, BARLIER A, GUNZ G et al. Pit-1 gene expression in the human pituitary adenomas. J Clin Endocrinol Metab 1994 ; 79 : 189-96.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 189-196
-
-
Pellegrini, I.1
Barlier, A.2
Gunz, G.3
-
83
-
-
0029794734
-
Pit-1 gene expression in human lactotroph and somatotroph pituitary adenomas is correlated to D2 receptor gene expression
-
PELLEGRINI I, MORANGE-RAMOS I, BARLIER A et al. Pit-1 gene expression in human lactotroph and somatotroph pituitary adenomas is correlated to D2 receptor gene expression. J Clin Endocrinol Metab 1996 ; 81 : 3390-6.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3390-3396
-
-
Pellegrini, I.1
Morange-Ramos, I.2
Barlier, A.3
-
84
-
-
0029787845
-
A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency
-
PELLEGRINI-BOUILLER I, BÉLICAR P, BARLIER A et al. A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency. J Clin Endocrinol Metab 1996 ; 81 : 2790-6.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 2790-2796
-
-
Pellegrini-Bouiller, I.1
Bélicar, P.2
Barlier, A.3
-
86
-
-
0028080819
-
Molecular basis of familial growth hormone deficiency
-
PEREZ JURADO LA, ARGENTE J. Molecular basis of familial growth hormone deficiency. Horm Res 1994 ; 42 : 189-97
-
(1994)
Horm Res
, vol.42
, pp. 189-197
-
-
Perez Jurado, L.A.1
Argente, J.2
-
87
-
-
6844243109
-
Combined pituitary hormone deficiency caused by a new Pit-1 mutation
-
San Francisco
-
PERNASETTI F, MILNER RDG, ASHWAL AA, LECOQ P, MARTIAL JA. Combined pituitary hormone deficiency caused by a new Pit-1 mutation. Tenth international congress of endocrinology, San Francisco, 1996 ; 955.
-
(1996)
Tenth International Congress of Endocrinology
, pp. 955
-
-
Pernasetti, F.1
Milner, R.D.G.2
Ashwal, A.A.3
Lecoq, P.4
Martial, J.A.5
-
88
-
-
0026667857
-
Mutation of the POU-Specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia
-
PFAFFLE RW, DIMATTIA GE, PARKS JS et al. Mutation of the POU-Specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia, Science 1992 ; 257 : 1118-21.
-
(1992)
Science
, vol.257
, pp. 1118-1121
-
-
Pfaffle, R.W.1
Dimattia, G.E.2
Parks, J.S.3
-
89
-
-
0027742950
-
Pit-1 and pituitary function
-
PFAFFLE RW, PARKS JS, BROWN MR, HEIMANN G, Pit-1 and pituitary function. J Pediatr Endocrinol 1993 , 6 : 229-33.
-
(1993)
J Pediatr Endocrinol
, vol.6
, pp. 229-233
-
-
Pfaffle, R.W.1
Parks, J.S.2
Brown, M.R.3
Heimann, G.4
-
90
-
-
0028246292
-
Pituitary hormones as neurotrophic signals : Anomalous hypophysiotropic neuron differentiation in hypopituitary dwarf mice
-
PHELPS CJ. Pituitary hormones as neurotrophic signals : anomalous hypophysiotropic neuron differentiation in hypopituitary dwarf mice. Proc Soc Exp Biol Med 1994 ; 206 : 6-23.
-
(1994)
Proc Soc Exp Biol Med
, vol.206
, pp. 6-23
-
-
Phelps, C.J.1
-
91
-
-
0027982794
-
Molecular basis of familial human growth hormone deficiency
-
PHILIPPS JA, COGAN JD. Molecular basis of familial human growth hormone deficiency. J Clin Endocrinol Metab 1994 ; 78 . 11-6
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 11-16
-
-
Philipps, J.A.1
Cogan, J.D.2
-
93
-
-
85060770827
-
Congenital complete absence of GH, TSH, ans PRL in infant : A consequence of Pit-1 gene deletion
-
PREEYASOMBAT C, SUPRASONSIN C, CHITANUPHAB A et al. Congenital complete absence of GH, TSH, ans PRL in infant : a consequence of Pit-1 gene deletion J Med Assoc Thai 1993 ; 76 Suppl 2 : 73-5.
-
(1993)
J Med Assoc Thai
, vol.76
, Issue.2 SUPPL.
, pp. 73-75
-
-
Preeyasombat, C.1
Suprasonsin, C.2
Chitanuphab, A.3
-
94
-
-
0029869857
-
The ontogeny of Pit-1 gene expression in the human fetal pituitary gland
-
PUY LA, ASA SL. The ontogeny of Pit-1 gene expression in the human fetal pituitary gland. Neuroendocrinol 1996 ; 63 349-55.
-
(1996)
Neuroendocrinol
, vol.63
, pp. 349-355
-
-
Puy, L.A.1
Asa, S.L.2
-
95
-
-
0026767630
-
A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency
-
RADOVICK S, NATIONS M, Du Y et al. A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency. Science 1992 ; 257 : 1115-8.
-
(1992)
Science
, vol.257
, pp. 1115-1118
-
-
Radovick, S.1
Nations, M.2
Du, Y.3
-
96
-
-
4243340117
-
Disorders of growth hormone and prolactin secretion
-
BERTRAND J, RAPPAPORT R, SIZONENKO PC Williams & Wilkins
-
RAPPAPORT R, CZERNICHOW P. Disorders of growth hormone and prolactin secretion. In : Pedriatric Endocrinology BERTRAND J, RAPPAPORT R, SIZONENKO PC Williams & Wilkins 1993 : 220-41.
-
(1993)
Pedriatric Endocrinology
, pp. 220-241
-
-
Rappaport, R.1
Czernichow, P.2
-
97
-
-
0029964808
-
Genetic mapping of the pituitary specific transcriptional factor gedne and its analysis in familial panhypopituitary warfism
-
RASKIN S, COGAN JD, SUMMAR ML et al Genetic mapping of the pituitary specific transcriptional factor gedne and its analysis in familial panhypopituitary warfism. Hum Genet 1996 ; 98 : 703-5.
-
(1996)
Hum Genet
, vol.98
, pp. 703-705
-
-
Raskin, S.1
Cogan, J.D.2
Summar, M.L.3
-
98
-
-
0027174997
-
A tissue-specific enhancer confers Pit-1 dependent morphogen inducibility and autoregulation on the Pit-1 gene
-
RHODES SJ, CHEN R, DIMATTIA GE A tissue-specific enhancer confers Pit-1 dependent morphogen inducibility and autoregulation on the Pit-1 gene. Genes Dev 1993 ; 7 : 913-32.
-
(1993)
Genes Dev
, vol.7
, pp. 913-932
-
-
Rhodes, S.J.1
Chen, R.2
Dimattia, G.E.3
-
99
-
-
0028138679
-
Transcriptional mechanisms in anterior pituitary cell differentiation
-
RHODES SJ, DIMATTIA GE, ROSENFELD MG. Transcriptional mechanisms in anterior pituitary cell differentiation. Curr Opinion Gen Dev 1994 ; 4 : 709-17.
-
(1994)
Curr Opinion Gen Dev
, vol.4
, pp. 709-717
-
-
Rhodes, S.J.1
Dimattia, G.E.2
Rosenfeld, M.G.3
-
100
-
-
0017125041
-
Congenital hypopthyroidisme in a young man with growth hormone, thyrotropin, and prolactin deficiencies
-
ROGOL AD, KAHN CR. Congenital hypopthyroidisme in a young man with growth hormone, thyrotropin, and prolactin deficiencies. J Pediair 1976 ; 88 : 953-8.
-
(1976)
J Pediair
, vol.88
, pp. 953-958
-
-
Rogol, A.D.1
Kahn, C.R.2
-
102
-
-
0027278607
-
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targering
-
RUGARLI EI, LUTZ B, KURATINI SC et al. Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targering. Nature Genet 1993 ; 4 : 19-26.
-
(1993)
Nature Genet
, vol.4
, pp. 19-26
-
-
Rugarli, E.I.1
Lutz, B.2
Kuratini, S.C.3
-
103
-
-
0015971263
-
A familial syndrome of isolated « aplasia » of the anterior pituitary
-
SADEGHI-NEJAD A, SENIOR B. A familial syndrome of isolated « aplasia » of the anterior pituitary. J Pediatr 1974 ; 84 : 79-84.
-
(1974)
J Pediatr
, vol.84
, pp. 79-84
-
-
Sadeghi-Nejad, A.1
Senior, B.2
-
104
-
-
0346206633
-
A hormonally controlled serum factor which stimulates sulfate incorporation by cartilage in vitro
-
SALMON WD, DAUGHADAY WH. A hormonally controlled serum factor which stimulates sulfate incorporation by cartilage in vitro. J Lab Clin Med 1957 ; 49 : 825-36
-
(1957)
J Lab Clin Med
, vol.49
, pp. 825-836
-
-
Salmon, W.D.1
Daughaday, W.H.2
-
105
-
-
0344480066
-
Analysis of the Pit-1 gene locus in a jamaican family with combined pituitary hormone deficiency
-
San Francisco
-
SANCHEZ JC, SCHIAVI A, PERERA E et al. Analysis of the Pit-1 gene locus in a jamaican family with combined pituitary hormone deficiency. International Congress of Endocrinology, San Francisco, 1996. P2-490.
-
(1996)
International Congress of Endocrinology
-
-
Sanchez, J.C.1
Schiavi, A.2
Perera, E.3
-
106
-
-
0028060189
-
The LIM domain : A new structural motif found in zinc-flinger-like proteins
-
SANCHEZ-GARCIA I, RABBITTS TH. The LIM domain : a new structural motif found in zinc-flinger-like proteins. Trends Genet 1994 ; 10 : 315-20.
-
(1994)
Trends Genet
, vol.10
, pp. 315-320
-
-
Sanchez-Garcia, I.1
Rabbitts, T.H.2
-
107
-
-
0002415079
-
Regulation of expression of the growth hormone and prolactin genes
-
IMURA H Raven Press
-
SCHAUFELE F. Regulation of expression of the growth hormone and prolactin genes. In : The Pituitary Gland, 2nd edition. IMURA H Raven Press 1994 ; 91-116.
-
(1994)
The Pituitary Gland, 2nd Edition
, pp. 91-116
-
-
Schaufele, F.1
-
108
-
-
0026639142
-
Synergistic activation of the rat growth hormone promoter by Pit-1 and the thyroid hormone receptor
-
SCHAUFELE F, WEST BL, BAXTER JD. Synergistic activation of the rat growth hormone promoter by Pit-1 and the thyroid hormone receptor. Mol Endocrinol 1992 ; 6 : 656-65.
-
(1992)
Mol Endocrinol
, vol.6
, pp. 656-665
-
-
Schaufele, F.1
West, B.L.2
Baxter, J.D.3
-
109
-
-
0028558774
-
The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuropithelium and persists in adult pituitary
-
SEIDAH NG, BARALE JC, MARCINKIEWICZ et al. The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuropithelium and persists in adult pituitary. DNA Cell Biol 1994 ; 13 : 1163-80.
-
(1994)
DNA Cell Biol
, vol.13
, pp. 1163-1180
-
-
Seidah, N.G.1
Barale, J.C.2
Marcinkiewicz3
-
110
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
SEMINA EV, REITER R, LEYSENS NJ et al. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nature Genet 1996 , 14 : 392-9.
-
(1996)
Nature Genet
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
-
111
-
-
9344229266
-
Specification of pituitary cell lineages by the LlM homeobox gene Lhx3
-
SHENZ HZ, ZHADANOV AB, MOSINGER B et al. Specification of pituitary cell lineages by the LlM homeobox gene Lhx3. Science 1996 ; 272 : 1004-7
-
(1996)
Science
, vol.272
, pp. 1004-1007
-
-
Shenz, H.Z.1
Zhadanov, A.B.2
Mosinger, B.3
-
112
-
-
10544256602
-
Pituitary lineage determination by the Porphet of Pit-1 homeodomain factor defective in Ames dwarfism
-
SORNSON MW, Wu W, DASEN JS et al. Pituitary lineage determination by the Porphet of Pit-1 homeodomain factor defective in Ames dwarfism. Nature 1996 ; 384 : 327-33.
-
(1996)
Nature
, vol.384
, pp. 327-333
-
-
Sornson, M.W.1
Wu, W.2
Dasen, J.S.3
-
113
-
-
0026345421
-
Thyrotropin-releasing hormone regulation of human TSHβ expression role of a pituitary-specific transcription factor (pit-1/GHF-1) and potential interaction with a thyroid hormone-inhibitory element
-
STEINFELDER HJ, HAUSER P, NAKAYMA Y et al. Thyrotropin-releasing hormone regulation of human TSHβ expression role of a pituitary-specific transcription factor (pit-1/GHF-1) and potential interaction with a thyroid hormone-inhibitory element. Proc Natl Acad Sci USA 1991 ; 88 : 3130-4.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 3130-3134
-
-
Steinfelder, H.J.1
Hauser, P.2
Nakayma, Y.3
-
114
-
-
0026754225
-
Hormonal regulation of the thyrotropin β-subunit gene by phosphorylation of the pituitary-specific transcription factor Pit-1
-
STEINFELDER HJ, RADOVICK S, WONDISFORD FE. Hormonal regulation of the thyrotropin β-subunit gene by phosphorylation of the pituitary-specific transcription factor Pit-1. Proc Natl Acad Sci USA 1992 ; 89 : 5942-5.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 5942-5945
-
-
Steinfelder, H.J.1
Radovick, S.2
Wondisford, F.E.3
-
115
-
-
0025853062
-
Somatotroph hypoplasia and dwarfism in transgenic mice expressing a nonphosphorylatable CREB mutant
-
STRUTHERS RS, VALE WW, ARIAS C, SAWCHENKO PE, MONTMINY MR. Somatotroph hypoplasia and dwarfism in transgenic mice expressing a nonphosphorylatable CREB mutant. Nature 1991 ; 350 : 622-4.
-
(1991)
Nature
, vol.350
, pp. 622-624
-
-
Struthers, R.S.1
Vale, W.W.2
Arias, C.3
Sawchenko, P.E.4
Montminy, M.R.5
-
116
-
-
0029780726
-
Isolated aplasia of the anterior pituitary gland with unusual associations
-
SULTAN Z, GNANARATNAM J, SHARIEF N. Isolated aplasia of the anterior pituitary gland with unusual associations. Clin Dysmorphol 1996 ; 5 : 347-50.
-
(1996)
Clin Dysmorphol
, vol.5
, pp. 347-350
-
-
Sultan, Z.1
Gnanaratnam, J.2
Sharief, N.3
-
117
-
-
0026849691
-
Cretinism with combined hormone deficiency caused by a mutation in the Pit1 gene
-
TATSUMI K, MIYAI K, NOTOMI T et al. Cretinism with combined hormone deficiency caused by a mutation in the Pit1 gene. Nature Genet 1992 ; 1 : 56-8.
-
(1992)
Nature Genet
, vol.1
, pp. 56-58
-
-
Tatsumi, K.1
Miyai, K.2
Notomi, T.3
-
118
-
-
0027733628
-
Transcriptional control of GH expression and anterior pituitary development
-
THEILL LE, KARIN M. Transcriptional control of GH expression and anterior pituitary development. Endocrine Rev 1993 ; 14 : 670-89.
-
(1993)
Endocrine Rev
, vol.14
, pp. 670-689
-
-
Theill, L.E.1
Karin, M.2
-
119
-
-
0030560899
-
The hypothalamic-pituitary axis : Co-development of two organs
-
TREIER M, ROSENFELD MG. The hypothalamic-pituitary axis : co-development of two organs. Curr Opinion Cell Biol 1996 ; 8 : 833-43.
-
(1996)
Curr Opinion Cell Biol
, vol.8
, pp. 833-843
-
-
Treier, M.1
Rosenfeld, M.G.2
-
121
-
-
0017727861
-
Prevalence of severe growth hormone deficiency
-
VIMPANI GI, ViMPANI AF, LIDGARD GP, CAMERON EHD, FARQUHAR JW. Prevalence of severe growth hormone deficiency. Br Med J 1977 ; 2 : 427-30.
-
(1977)
Br Med J
, vol.2
, pp. 427-430
-
-
Vimpani, G.I.1
Vimpani, A.F.2
Lidgard, G.P.3
Cameron, E.H.D.4
Farquhar, J.W.5
-
122
-
-
0026657816
-
Anterior pituitary development : Short tales from dwarf mice
-
Voss JW, ROSENFELD MG. Anterior pituitary development : short tales from dwarf mice Cell 1992 ; 70 : 527-30.
-
(1992)
Cell
, vol.70
, pp. 527-530
-
-
Voss, J.W.1
Rosenfeld, M.G.2
-
123
-
-
85003066076
-
An alternative Pit-1 RNA splicing product reveals modular binding and nonmodular transcriptional activities of the POU-specific domain
-
Voss JW, WILSON L, RHODES SJ. An alternative Pit-1 RNA splicing product reveals modular binding and nonmodular transcriptional activities of the POU-specific domain. Mol Endocrinol 1993 ; 7 : 1551-60.
-
(1993)
Mol Endocrinol
, vol.7
, pp. 1551-1560
-
-
Voss, J.W.1
Wilson, L.2
Rhodes, S.J.3
-
124
-
-
0030033150
-
Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse
-
WAJNRAJCH MP, GERTNER JM, HARBISON MD, CHUA SCJ, LEIBEL RL. Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse. Nature Genet 1996 ; 12 : 88-90.
-
(1996)
Nature Genet
, vol.12
, pp. 88-90
-
-
Wajnrajch, M.P.1
Gertner, J.M.2
Harbison, M.D.3
Chua, S.C.J.4
Leibel, R.L.5
-
125
-
-
0029819642
-
The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human
-
WALDSTREICHER J, SEMINARA SB, JAMESON JL et al. The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human. J Clin Endocrinol Metab 1996 ; 81 : 4388-95.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4388-4395
-
-
Waldstreicher, J.1
Seminara, S.B.2
Jameson, J.L.3
-
126
-
-
0029827345
-
Linkage of the gene for the triple. A syndrome to chromosome 12q13 near the type II keratin gene cluster
-
WEBER A, WIENKER TF, JUNG M et al. Linkage of the gene for the triple. A syndrome to chromosome 12q13 near the type II keratin gene cluster. Hum Mol Gen 1996 ; 5 : 2061-6.
-
(1996)
Hum Mol Gen
, vol.5
, pp. 2061-2066
-
-
Weber, A.1
Wienker, T.F.2
Jung, M.3
-
127
-
-
0027616283
-
POU-domain proteins : Structure and function of development regulators
-
WEGNER M, DROLET DW, ROSENFELD MG. POU-domain proteins : structure and function of development regulators. Curr Opinion Celle Biol 1993 ; 5 : 488-98.
-
(1993)
Curr Opinion Celle Biol
, vol.5
, pp. 488-498
-
-
Wegner, M.1
Drolet, D.W.2
Rosenfeld, M.G.3
-
128
-
-
6844226968
-
Isolated growth hormone deficiency and multiple pituitary deficiencies : Patient characteristics and 12-months treatment results. KIGS (Pharmacia & Upjohn International Growth Database)
-
WILTON P, LINDBERG A. Isolated growth hormone deficiency and multiple pituitary deficiencies : patient characteristics and 12-months treatment results. KIGS (Pharmacia & Upjohn International Growth Database) . Biannual report 1996 1996 ; 14 : 15-24.
-
(1996)
Biannual Report 1996
, vol.14
, pp. 15-24
-
-
Wilton, P.1
Lindberg, A.2
-
129
-
-
0016160118
-
Idiopathic sexual precocity in a boy with growth hormone, prolactin and thyrotropin deficiencies
-
WINTER JSD, DE GROOT GW, FAIMAN C. Idiopathic sexual precocity in a boy with growth hormone, prolactin and thyrotropin deficiencies. J Clin Endocrinol Metab 1974 ; 39 : 356-63.
-
(1974)
J Clin Endocrinol Metab
, vol.39
, pp. 356-363
-
-
Winter, J.S.D.1
De Groot, G.W.2
Faiman, C.3
-
130
-
-
0024953696
-
Total deficiency of growth hormone and prolactin. and partial deficiency of thyroid stimulating hormone in two dutch families : A new variant of hereditary pituitary deficiency
-
WIT JM, DRAYER NM, JANSEN M et al. Total deficiency of growth hormone and prolactin. and partial deficiency of thyroid stimulating hormone in two dutch families : a new variant of hereditary pituitary deficiency. Horm Res 1989 ; 32 : 170-7.
-
(1989)
Horm Res
, vol.32
, pp. 170-177
-
-
Wit, J.M.1
Drayer, N.M.2
Jansen, M.3
-
131
-
-
0029910994
-
Cloning and sequence analysis of the human gene encoding steroidogenic factor 1
-
WONG M, RAMAYYA MS, CHROUSOS GP, DRIGGERS PH, PARKER KL. Cloning and sequence analysis of the human gene encoding steroidogenic factor 1. J Mol Endocrinol 1996 ; 17 : 139-47.
-
(1996)
J Mol Endocrinol
, vol.17
, pp. 139-147
-
-
Wong, M.1
Ramayya, M.S.2
Chrousos, G.P.3
Driggers, P.H.4
Parker, K.L.5
-
132
-
-
6844228046
-
-
The Endocrine Society, San Francisco
-
WOODS KA, CAMACHO-HUBNER C, SAVAGE MO, CLARK AJL. Intrauterine growth retardation and postnatal growth failure in a patient homozygous for a partial IGF-1 gene deletion. The Endocrine Society, San Francisco, 1996 ; 2 : 709.
-
(1996)
Intrauterine Growth Retardation and Postnatal Growth Failure in a Patient Homozygous for a Partial IGF-1 Gene Deletion
, vol.2
, pp. 709
-
-
Woods, K.A.1
Camacho-Hubner, C.2
Savage, M.O.3
Clark, A.J.L.4
-
134
-
-
0025988994
-
Mediation by calcium of thyrotropin-releasing hormone action on the prolactin promoter via transcription factor Pit-1
-
YAN G-Z, BANCROFT C Mediation by calcium of thyrotropin-releasing hormone action on the prolactin promoter via transcription factor Pit-1. Mol Endocrinol 1991 , 5 : 1488-97.
-
(1991)
Mol Endocrinol
, vol.5
, pp. 1488-1497
-
-
Yan, G.-Z.1
Bancroft, C.2
-
135
-
-
0025666976
-
A case of severe pituitary dwarfism associated with prolactin and thyroid stimulating hormone deficiences
-
YOSHIMOTO M, KINOSHITA E, BABA T et al. A case of severe pituitary dwarfism associated with prolactin and thyroid stimulating hormone deficiences. Acta Paediatr Scand 1990 ; 79 : 1247-51.
-
(1990)
Acta Paediatr Scand
, vol.79
, pp. 1247-1251
-
-
Yoshimoto, M.1
Kinoshita, E.2
Baba, T.3
-
136
-
-
0017610556
-
Variable X-linked recessive hypopituitarism with evidence of gonadotropin deficiency in two pre-pubertal males
-
ZIPF WB, KELCH RP, BACON GE. Variable X-linked recessive hypopituitarism with evidence of gonadotropin deficiency in two pre-pubertal males. Clin Genet 1977 , 1 : 249-54.
-
(1977)
Clin Genet
, vol.1
, pp. 249-254
-
-
Zipf, W.B.1
Kelch, R.P.2
Bacon, G.E.3
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