-
1
-
-
0026849691
-
Cretinism with combined hormone deficiency caused by a mutation in the Pit-1 gene
-
Tatsumi K, Miyai K, Notomi T, Kaibe K, Amino N. 1992 Cretinism with combined hormone deficiency caused by a mutation in the Pit-1 gene. Nature Genet 1, 56-58
-
(1992)
Nature Genet
, vol.1
, pp. 56-58
-
-
Tatsumi, K.1
Miyai, K.2
Notomi, T.3
Kaibe, K.4
Amino, N.5
-
2
-
-
0025014024
-
Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene Pit-1
-
Li S, Crenshaw III E.B., Rawson EJ, Simmons DM, Swanson LW, Rosenfeld MG. 1990 Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene Pit-1. Nature 347, 528-533
-
(1990)
Nature
, vol.347
, pp. 528-533
-
-
Li, S.1
Crenshaw III, E.B.2
Rawson, E.J.3
Simmons, D.M.4
Swanson, L.W.5
Rosenfeld, M.G.6
-
3
-
-
10544256602
-
Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism
-
Sornson MW, Wu W, Dasen JS, Flynn SE, Norman DJ, O'Connell SM, Gukovsky I, Carriere C, Ryan AK, Miller AP, Zuo L, Gleiberman AS, Andersen B, Beamer WG, Rosenfeld MG. 1996 Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism. Nature 384, 327-333
-
(1996)
Nature
, vol.384
, pp. 327-333
-
-
Sornson, M.W.1
Wu, W.2
Dasen, J.S.3
Flynn, S.E.4
Norman, D.J.5
O'Connell, S.M.6
Gukovsky, I.7
Carriere, C.8
Ryan, A.K.9
Miller, A.P.10
Zuo, L.11
Gleiberman, A.S.12
Andersen, B.13
Beamer, W.G.14
Rosenfeld, M.G.15
-
4
-
-
0025272043
-
A family of POU domain and Pit-1 tissue-specific transcription factors in pituitary and neuroendocrine development
-
Ingraham HA, Albert VR, Chen R, Crenshaw III EB, Elsholtz HP, He X, Kapiloff MS, Mangalam HJ, Swanson LW, Treacy MN, Rosenfeld MG. 1990 A family of POU domain and Pit-1 tissue-specific transcription factors in pituitary and neuroendocrine development. Annu. Rev. Physiol. 52,773-791
-
(1990)
Annu. Rev. Physiol.
, vol.52
, pp. 773-791
-
-
Ingraham, H.A.1
Albert, V.R.2
Chen, R.3
Crenshaw III, E.B.4
Elsholtz, H.P.5
He, X.6
Kapiloff, M.S.7
Mangalam, H.J.8
Swanson, L.W.9
Treacy, M.N.10
Rosenfeld, M.G.11
-
5
-
-
0025735101
-
POU-domain transcription factors: Powerful developemental regulators
-
Rosenfeld MG. 1991 POU-domain transcription factors: powerful developemental regulators. Gene & Development 5: 897-907
-
(1991)
Gene & Development
, vol.5
, pp. 897-907
-
-
Rosenfeld, M.G.1
-
6
-
-
0029608970
-
The Ames dwarf gene is required for Pit-1 gene activation
-
Andersen B, Pearse II RV, Jenne K, Sornson M, Lin SC, Bartke A, Rosenfeld MG. 1995 The Ames dwarf gene is required for Pit-1 gene activation. Dev Biol 172, 495-503
-
(1995)
Dev Biol
, vol.172
, pp. 495-503
-
-
Andersen, B.1
Pearse II, R.V.2
Jenne, K.3
Sornson, M.4
Lin, S.C.5
Bartke, A.6
Rosenfeld, M.G.7
-
7
-
-
0025969025
-
Regulation of transcription and cell identity by POU domain proteins
-
Ruvkin G, Finney M. 1991 Regulation of transcription and cell identity by POU domain proteins. Cell 64: 475-478
-
(1991)
Cell
, vol.64
, pp. 475-478
-
-
Ruvkin, G.1
Finney, M.2
-
8
-
-
0027236844
-
Molecular basis of the little mouse phenotype and implications for cell type-specific growth
-
Lin SC, Lin CR, Gukovsky I, Lusis AJ, Sawchenko PE, Rosenfeld MG. 1993 Molecular basis of the little mouse phenotype and implications for cell type-specific growth. Nature 364, 208-213
-
(1993)
Nature
, vol.364
, pp. 208-213
-
-
Lin, S.C.1
Lin, C.R.2
Gukovsky, I.3
Lusis, A.J.4
Sawchenko, P.E.5
Rosenfeld, M.G.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. 1992 A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency. Science 257,1115-1118
-
(1992)
Science
, vol.257
, pp. 1115-1118
-
-
Radovick, S.1
Nations, M.2
Du, Y.3
Berg, L.A.4
Weintraub, B.D.5
Wondisford, F.E.6
-
10
-
-
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, Van der Nat H, Van den Brande JL, Rosenfeld MG, Ingraham HA. 1992 Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Science 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
Van Der Nat, H.7
Van Den Brande, J.L.8
Rosenfeld, M.G.9
Ingraham, H.A.10
-
11
-
-
0002005882
-
Abnormalities of the pituitary-specific transcription factor-1 gene and protein
-
Parks JS, Brown MR, Abdul-Latif H, Kinoshita E. 1995 Abnormalities of the pituitary-specific transcription factor-1 gene and protein. Clin Pediatr Endocrinol4, 33-39
-
(1995)
Clin Pediatr Endocrinol
, vol.4
, pp. 33-39
-
-
Parks, J.S.1
Brown, M.R.2
Abdul-Latif, H.3
Kinoshita, E.4
-
12
-
-
0027980595
-
Monoallelic expression of normal mRNA in the PIT1 mutation heterozygous withnormal phenotype and biallelic expression in the abnormal phenotype
-
Okamoto N, Wada Y, Ida S, Koga R, Ozono K, Chiyo H, Hayashi A, Tatsumi K. 1994 Monoallelic expression of normal mRNA in the PIT1 mutation heterozygous withnormal phenotype and biallelic expression in the abnormal phenotype. Hum Mol Genet 3: 1565-1568
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1565-1568
-
-
Okamoto, N.1
Wada, Y.2
Ida, S.3
Koga, R.4
Ozono, K.5
Chiyo, H.6
Hayashi, A.7
Tatsumi, K.8
-
13
-
-
17344371881
-
Mutations in PROP1 cause familial combined pituitary hormone deficiency
-
Wu W, Cogan JD, Pfaffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JAIII, Rosenfeld MG. 1998 Mutations in PROP1 cause familial combined pituitary hormone deficiency. Nature Genet 18: 147-149
-
(1998)
Nature Genet
, vol.18
, pp. 147-149
-
-
Wu, W.1
Cogan, J.D.2
Pfaffle, R.W.3
Dasen, J.S.4
Frisch, H.5
O'Connell, S.M.6
Flynn, S.E.7
Brown, M.R.8
Mullis, P.E.9
Parks, J.S.10
Phillips III, J.A.11
Rosenfeld, M.G.12
-
14
-
-
0032034425
-
A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency
-
in press
-
Fofanova OV, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency. Pituitary (in press).
-
Pituitary
-
-
Fofanova, O.V.1
Takamura, N.2
Kinoshita, E.3
Parks, J.S.4
Brown, M.R.5
Peterkova, V.A.6
Evgrafov, O.V.7
Goncharov, N.P.8
Bulatov, A.A.9
Dedov, I.I.10
Yamashita, S.11
-
15
-
-
17544393646
-
Rarity of Pit-1 gene involvement in children from Russia with combined pituitary hormone deficiency
-
in press
-
Fofanova OV, Takamura N, Kinoshita E, Yoshimoto M, Tsuji Y, Peterkova OV, Evgrafov V, Dedov II, Goncharov NP, Yamashita S. Rarity of Pit-1 gene involvement in children from Russia with combined pituitary hormone deficiency. Am J Med Genet (in press).
-
Am J Med Genet
-
-
Fofanova, O.V.1
Takamura, N.2
Kinoshita, E.3
Yoshimoto, M.4
Tsuji, Y.5
Peterkova, O.V.6
Evgrafov, V.7
Dedov, I.I.8
Goncharov, N.P.9
Yamashita, S.10
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