-
1
-
-
0025240831
-
Expression of GHF-1 protein in mouse pituitaries correlates both temporally and spatially with the onset of growth hormone gene activity
-
Dolle P, Gastrillo JL, Theill LE, Deerinck T, Ellisman M & Karin M. Expression of GHF-1 protein in mouse pituitaries correlates both temporally and spatially with the onset of growth hormone gene activity. Cell 1990 60 809-820.
-
(1990)
Cell
, vol.60
, pp. 809-820
-
-
Dolle, P.1
Gastrillo, J.L.2
Theill, L.E.3
Deerinck, T.4
Ellisman, M.5
Karin, M.6
-
2
-
-
0025286831
-
Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors
-
Simmons DM, Voss JW, Ingraham HA, Holloway JM, Broide RS, Rosenfeld MG et al. Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors. Genes and Development 1999 4 695-711.
-
(1999)
Genes and Development
, vol.4
, pp. 695-711
-
-
Simmons, D.M.1
Voss, J.W.2
Ingraham, H.A.3
Holloway, J.M.4
Broide, R.S.5
Rosenfeld, M.G.6
-
3
-
-
0030918673
-
POU domain family values: Flexibility, partnerships and developmental codes
-
Ryan AK & Rosenfeld MG. POU domain family values: flexibility, partnerships and developmental codes. Genes and Development 1997 11 1207-1225.
-
(1997)
Genes and Development
, vol.11
, pp. 1207-1225
-
-
Ryan, A.K.1
Rosenfeld, M.G.2
-
4
-
-
0027174997
-
A tissue-specific enhancer confers Pit-1-dependent morphogen inducibility and autoregulation on the Pit-1 gene
-
Rhodes SJ, Chen R, DiMattia GE, Scully KM, Kalla KA, Lin S et al. A tissue-specific enhancer confers Pit-1-dependent morphogen inducibility and autoregulation on the Pit-1 gene. Genes and Development 1993 7 913-932.
-
(1993)
Genes and Development
, vol.7
, pp. 913-932
-
-
Rhodes, S.J.1
Chen, R.2
DiMattia, G.E.3
Scully, K.M.4
Kalla, K.A.5
Lin, S.6
-
5
-
-
0025014024
-
Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene Pit-1
-
Li S, Crenshaw EB III, Rawson EJ, Simmons DM, Swanson LW & Rosenfeld MG. Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene Pit-1. Nature 1990 347 528-533.
-
(1990)
Nature
, vol.347
, pp. 528-533
-
-
Li, S.1
Crenshaw E.B. III2
Rawson, E.J.3
Simmons, D.M.4
Swanson, L.W.5
Rosenfeld, M.G.6
-
6
-
-
0027076516
-
Pit-1-dependent expression of the receptor for growth hormone releasing factor mediates pituitary cell growth
-
Lin C, Lin SC, Chang CP & Rosenfeld MG. Pit-1-dependent expression of the receptor for growth hormone releasing factor mediates pituitary cell growth. Nature 1992 360 765-768.
-
(1992)
Nature
, vol.360
, pp. 765-768
-
-
Lin, C.1
Lin, S.C.2
Chang, C.P.3
Rosenfeld, M.G.4
-
7
-
-
0032230229
-
Structure and regulation of the human growth hormone-releasing hormone receptor gene
-
Petersenn S, Rasche AC, Heyens M & Schulte H. Structure and regulation of the human growth hormone-releasing hormone receptor gene. Molecular Endocrinology 1998 12 233-247.
-
(1998)
Molecular Endocrinology
, vol.12
, pp. 233-247
-
-
Petersenn, S.1
Rasche, A.C.2
Heyens, M.3
Schulte, H.4
-
8
-
-
0033597229
-
Cloning and characterization of the 5′-flanking region of the human growth hormone-releasing hormone receptor gene
-
Iguchi G, Okimura Y, Takahashi T, Mizuno I, Fumoto M, Takahashi Y et al. Cloning and characterization of the 5′-flanking region of the human growth hormone-releasing hormone receptor gene. Journal of Biological Chemistry 1999 274 12108-12114.
-
(1999)
Journal of Biological Chemistry
, vol.274
, pp. 12108-12114
-
-
Iguchi, G.1
Okimura, Y.2
Takahashi, T.3
Mizuno, I.4
Fumoto, M.5
Takahashi, Y.6
-
9
-
-
0026767630
-
A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency
-
Radovick S, Nations M, Du Y, Berg LA, Weintraub BD & Wondisford FE. A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency. Science 1992 257 1115-1121.
-
(1992)
Science
, vol.257
, pp. 1115-1121
-
-
Radovick, S.1
Nations, M.2
Du, Y.3
Berg, L.A.4
Weintraub, B.D.5
Wondisford, F.E.6
-
10
-
-
0027080611
-
Mutations in the PIT-1 gene in children with combined pituitary hormone deficiency
-
Ohta K, Nobukuni Y, Mitsubuchi H, Fujimoto S, Matsuo N, Inagaki H et al. Mutations in the PIT-1 gene in children with combined pituitary hormone deficiency. Biochemical and Biophysical Research Communications 1992 189 851-855.
-
(1992)
Biochemical and Biophysical Research Communications
, vol.189
, pp. 851-855
-
-
Ohta, K.1
Nobukuni, Y.2
Mitsubuchi, H.3
Fujimoto, S.4
Matsuo, N.5
Inagaki, H.6
-
11
-
-
0027980595
-
Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype
-
Okamoto N, Wada Y, Ida S, Koga R, Ozono K, Chiyo H et al. Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype. Human Molecular Genetics 1994 3 1565-1568.
-
(1994)
Human Molecular Genetics
, vol.3
, pp. 1565-1568
-
-
Okamoto, N.1
Wada, Y.2
Ida, S.3
Koga, R.4
Ozono, K.5
Chiyo, H.6
-
12
-
-
0029014128
-
Screening for PIT1 abnormality by PCR direct sequencing method
-
Irie Y, Tatsumi K, Kusuda S, Kawasaki H, Boyages SC, Nose O et al. Screening for PIT1 abnormality by PCR direct sequencing method. Thyroid 1995 5 207-211.
-
(1995)
Thyroid
, vol.5
, pp. 207-211
-
-
Irie, Y.1
Tatsumi, K.2
Kusuda, S.3
Kawasaki, H.4
Boyages, S.C.5
Nose, O.6
-
15
-
-
0028865778
-
The prenatal role of thyroid hormone evidenced by fetomaternal Pit-1 deficiency
-
de Zegher F, Pernasetti F, Vanhole C, Devlieger H, Berghe GV & Martial JA. The prenatal role of thyroid hormone evidenced by fetomaternal Pit-1 deficiency. Journal of Clinical Endocrinology and Metabolism 1995 80 3127-3130.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 3127-3130
-
-
de Zegher, F.1
Pernasetti, F.2
Vanhole, C.3
Devlieger, H.4
Berghe, G.V.5
Martial, J.A.6
-
16
-
-
0028980503
-
A hot spot in the Pit-1 gene responsible for combined pituitary hormone deficiency: Clinical and molecular correlates
-
Cohen LE, Wondisford FE, Saivatoni A, Maghnie M, Brucker-Davis F, Weintraub BD et al. A hot spot in the Pit-1 gene responsible for combined pituitary hormone deficiency: clinical and molecular correlates. Journal of Clinical Endocrinology and Metabolism 1995 80 679-684.
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, pp. 679-684
-
-
Cohen, L.E.1
Wondisford, F.E.2
Saivatoni, A.3
Maghnie, M.4
Brucker-Davis, F.5
Weintraub, B.D.6
-
18
-
-
0030834444
-
Combined pituitary deficiencies of growth hormone, thyroid stimulating hormone and prolactin due to Pit-1 gene mutation: A case report
-
Holl RW, Pfaffle R, Kim C, Sorgo W, Teller WM & Heimann G. Combined pituitary deficiencies of growth hormone, thyroid stimulating hormone and prolactin due to Pit-1 gene mutation: a case report. European Journal of Pediatrics 1997 156 835-837.
-
(1997)
European Journal of Pediatrics
, vol.156
, pp. 835-837
-
-
Holl, R.W.1
Pfaffle, R.2
Kim, C.3
Sorgo, W.4
Teller, W.M.5
Heimann, G.6
-
19
-
-
0031812218
-
Severe congenital hypopituitarism with low prolactin levels and age-dependent anterior pituitary hypoplasia: A clue to a PIT-1 mutation
-
Ward L, Chavez M, Huot C, Lecocq P, Collu R, Decarie JC et al. Severe congenital hypopituitarism with low prolactin levels and age-dependent anterior pituitary hypoplasia: a clue to a PIT-1 mutation. Journal of Pediatrics 1998 132 1036-1038.
-
(1998)
Journal of Pediatrics
, vol.132
, pp. 1036-1038
-
-
Ward, L.1
Chavez, M.2
Huot, C.3
Lecocq, P.4
Collu, R.5
Decarie, J.C.6
-
20
-
-
0032911188
-
Defective retinoic acid regulation of the Pit-1 gene enhancer: A novel mechanism of combined pituitary hormone deficiency
-
Cohen LE, Zanger K, Brue T, Wondisford FE & Radovick S. Defective retinoic acid regulation of the Pit-1 gene enhancer: a novel mechanism of combined pituitary hormone deficiency. Molecular Endocrinology 1999 13 476-484.
-
(1999)
Molecular Endocrinology
, vol.13
, pp. 476-484
-
-
Cohen, L.E.1
Zanger, K.2
Brue, T.3
Wondisford, F.E.4
Radovick, S.5
-
21
-
-
0031732644
-
Pro239Ser: A novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency
-
Pernasetti F, Milner R, Al Ashwal A, Zegher F, Chavez VM, Muller M et al. Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency. Journal of Clinical Endocrinology and Metabolism 1998 83 2079-2083.
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, pp. 2079-2083
-
-
Pernasetti, F.1
Milner, R.2
Al Ashwal, A.3
Zegher, F.4
Chavez, V.M.5
Muller, M.6
-
22
-
-
0029787845
-
A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency
-
Pellegrini-Bouiller I, Belicar P, Barlier A, Gunz G, Charvet JP, Jaquet P et al. A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency. Journal of Clinical Endocrinology and Metabolism 1996 81 2790-2796.
-
(1996)
Journal of Clinical Endocrinology and Metabolism
, vol.81
, pp. 2790-2796
-
-
Pellegrini-Bouiller, I.1
Belicar, P.2
Barlier, A.3
Gunz, G.4
Charvet, J.P.5
Jaquet, P.6
-
23
-
-
0031963636
-
Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene
-
Brown MR, Parks JS, Adess ME, Rich BH, Rosenthal IM, Voss TC et al. Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. Hormone Research 1998 49 98-102.
-
(1998)
Hormone Research
, vol.49
, pp. 98-102
-
-
Brown, M.R.1
Parks, J.S.2
Adess, M.E.3
Rich, B.H.4
Rosenthal, I.M.5
Voss, T.C.6
-
24
-
-
0029121819
-
A novel E250X mutation of the PIT1 gene in a patient with combined pituitary hormone deficiency
-
Irie Y, Tatsumi K, Ogawa M, Kamijo T, Preeyasombat C, Suprasongsin C et al. A novel E250X mutation of the PIT1 gene in a patient with combined pituitary hormone deficiency. Endocrine Journal 1995 42 351-354.
-
(1995)
Endocrine Journal
, vol.42
, pp. 351-354
-
-
Irie, Y.1
Tatsumi, K.2
Ogawa, M.3
Kamijo, T.4
Preeyasombat, C.5
Suprasongsin, C.6
-
25
-
-
0026667857
-
Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia
-
Pfaffle RW, DiMattia GE, Parks JS, Brown MR, Wit JM, Jansen M et al. Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Science 1992 257 1118-1121.
-
(1992)
Science
, vol.257
, pp. 1118-1121
-
-
Pfaffle, R.W.1
DiMattia, G.E.2
Parks, J.S.3
Brown, M.R.4
Wit, J.M.5
Jansen, M.6
-
26
-
-
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. Endocrinology and Metabolism Clinics of North America 1996 25 523-540.
-
(1996)
Endocrinology and Metabolism Clinics of North America
, vol.25
, pp. 523-540
-
-
Cohen, L.E.1
Wondisford, F.E.2
Radovick, S.3
-
27
-
-
0026849691
-
Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene
-
Tatsumi K, Miyai K, Notomi T, Kaibe K, Amino N, Mizuno Y et al. Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene. Nature Genetics 1992 1 56-58.
-
(1992)
Nature Genetics
, vol.1
, pp. 56-58
-
-
Tatsumi, K.1
Miyai, K.2
Notomi, T.3
Kaibe, K.4
Amino, N.5
Mizuno, Y.6
-
28
-
-
0035030696
-
Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POUF1 gene
-
Hendriks-Stegeman BI, Augustijn KD, Bakker B, Holthuizen P, Van Der Vliet PC & Jansen M. Combined pituitary hormone deficiency caused by compound heterozygosity for two novel mutations in the POU domain of the PIT1/POUF1 gene. Journal of Clinical Endocrinology and Metabolism 2001 86 1545-1550.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 1545-1550
-
-
Hendriks-Stegeman, B.I.1
Augustijn, K.D.2
Bakker, B.3
Holthuizen, P.4
Van Der Vliet, P.C.5
Jansen, M.6
-
29
-
-
0037160133
-
Novel function of transactivation domain of a pituitary specific transcription factor Pit-1
-
Kishimoto M, Okimura Y, Yagita K, Iguchi G, Fumoto M, Iida K et al. Novel function of transactivation domain of a pituitary specific transcription factor Pit-1. Journal of Biological Chemistry 2002 277 45141-45148.
-
(2002)
Journal of Biological Chemistry
, vol.277
, pp. 45141-45148
-
-
Kishimoto, M.1
Okimura, Y.2
Yagita, K.3
Iguchi, G.4
Fumoto, M.5
Iida, K.6
-
31
-
-
0035721198
-
A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminus
-
Blankenstein O, Muhlenberg R, Kim C, Wuller S, Pfaffle R & Heimann G. A new C-terminal located mutation (V272ter) in the PIT-1 gene manifesting with severe congenital hypothyroidism. Possible functionality of the PIT-1 C-terminus. Hormone Research 2002 56 81-86.
-
(2002)
Hormone Research
, vol.56
, pp. 81-86
-
-
Blankenstein, O.1
Muhlenberg, R.2
Kim, C.3
Wuller, S.4
Pfaffle, R.5
Heimann, G.6
-
32
-
-
0035117485
-
POU domain factors in the neuroendocrine system: Lessons from developmental biology provide insights into disease
-
Andersen B & Rosenfeld MG. POU domain factors in the neuroendocrine system: lessons from developmental biology provide insights into disease. Endocrine Reviews 2001 22 2-35.
-
(2001)
Endocrine Reviews
, vol.22
, pp. 2-35
-
-
Andersen, B.1
Rosenfeld, M.G.2
|