-
3
-
-
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
-
(1996)
Development
, vol.122
, pp. 41-52
-
-
Hermesz, E.1
Mackem, S.2
Mahon, A.3
-
6
-
-
0032230271
-
The pan-pituitary activator of transcription. Ptx1 (pituitary homeobox 1), acts in synergy with SF-1 and Pit-1 and is an upstream activator of the Lim-homeodomain gene Lim3/Lhx3
-
(1998)
Mol Endocrinol
, vol.12
, pp. 428-441
-
-
Tremblay, J.J.1
Lanctot, C.2
Drouin, J.3
-
7
-
-
0035937414
-
A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins
-
(2001)
Cell
, vol.104
, pp. 849-959
-
-
Lamolet, B.1
Pulichino, A.M.2
Lamonerie, T.3
Gauthier, Y.4
Brue, T.5
Enjalbert, A.6
Drouin, J.7
-
8
-
-
0035902499
-
Tbx19, a tissue-selective regulator of POMC gene expression
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 8674-8679
-
-
Liu, J.1
Lin, C.2
Gleiberman, A.3
Herman, T.4
Huang, H.P.5
Tsai, M.J.6
Rosenfeld, M.G.7
-
9
-
-
0031043428
-
Pituitary homeobox 2, a novel member of the bicoid related family of homeobox genes, is a potential regulator of anterior structure formation
-
(1997)
Hum Mol Genet
, vol.6
, pp. 457-464
-
-
Gage, P.J.1
Camper, S.A.2
-
11
-
-
0030776222
-
Expression pattern of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation
-
(1997)
Mech Dev
, vol.67
, pp. 83-96
-
-
Kitamura, K.1
Miura, H.2
Yanazawa, M.3
Miyashita, T.4
Kato, K.5
-
12
-
-
0032516096
-
Identification and characterization of the Arp1 gene, a target for the human acute leukemia ALL1 gene
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 4573-4578
-
-
Arakawa, H.1
Nakamura, T.2
Zhadanov, A.B.3
Fidanza, V.4
Yano, T.5
Bullrich, F.6
Shimizu, M.7
Blechman, J.8
Mazo, A.9
Canaani, E.10
Croce, C.M.11
-
14
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
(1996)
Nat Genet
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
Carey, J.C.11
Murray, J.C.12
-
16
-
-
0033575971
-
Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis
-
(1999)
Nature
, vol.401
, pp. 279-282
-
-
Lin, C.R.1
Kioussi, C.2
O'Connell, S.3
Briata, P.4
Szeto, D.5
Liu, F.6
Izpisua-Belmonte, J.C.7
Rosenfeld, M.G.8
-
19
-
-
0033387975
-
Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism
-
(1999)
Development
, vol.126
, pp. 5749-5758
-
-
Kitamura, K.1
Miura, H.2
Miyagawa-Tomita, S.3
Yanazawa, M.4
Katoh-Fukui, Y.5
Suzuki, R.6
Ohuchi, H.7
Suehiro, A.8
Motegi, Y.9
Nakahara, Y.10
Kondo, S.11
Yokoyama, M.12
-
27
-
-
0032940188
-
Egr-1 is a downstream effector of GnRH and synergizes by direct interaction with Ptx1 and SF-1 to enhance luteinizing hormone-gene transcription
-
(1999)
Mol Cell Biol
, vol.19
, pp. 2567-2576
-
-
Tremblay, J.J.1
Drouin, J.2
-
28
-
-
0028126819
-
Pit-1 determines cell types during development of the anterior pituitary gland. A model for transcriptional regulation of cell phenotypes in mammalian organogenesis
-
(1994)
J Biol Chem
, vol.269
, pp. 29335-29338
-
-
Andersen, B.1
Rosenfeld, M.G.2
-
31
-
-
0033557807
-
Role of the bicoid-related homeodomain factor Pitx1 in specifying hindlimb morphogenesis and pituitary development
-
(1999)
Genes Dev
, vol.13
, pp. 484-494
-
-
Szeto, D.P.1
Rodriguez-Esteban, C.2
Ryan, A.K.3
O'Connell, S.M.4
Liu, F.5
Kioussi, C.6
Gleiberman, A.S.7
Izpisua-Belmonte, J.C.8
Rosenfeld, M.G.9
-
38
-
-
0035423316
-
Functional analysis of two newly identified Pitx2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1631-1638
-
-
Priston, M.1
Kozlowski, K.2
Gill, D.3
Letwin, K.4
Buys, Y.5
Levin, A.V.6
Walter, M.A.7
Heon, E.8
-
40
-
-
17344371881
-
Mutations in Prop1 cause familial combined hormone deficiency
-
(1998)
Nat Genet
, vol.18
, pp. 147-150
-
-
Wu, W.1
Cogan, J.D.2
Pfäffle, 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 J.A. III11
Rosenfeld, M.G.12
-
41
-
-
0034040904
-
Mutations in LHX3 results in a new syndrome revealed by combines pituitary hormone deficiency
-
(2000)
Nat Genet
, vol.25
, pp. 182-186
-
-
Netchine, I.1
Sobrier, M.L.2
Krude, H.3
Schnabel, D.4
Maghnie, M.5
Marcos, E.6
Duriez, B.7
Cacheux, V.8
Moers, A.9
Goossens, M.10
Gruters, A.11
Amselem, S.12
-
42
-
-
0029787845
-
A transcription factor Pit-1 is responsible for combined pituitary hormone deficiency
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 2790-2796
-
-
Pellegrini-Bouiller, I.1
Bélicar, P.2
Barlier, A.3
Gunz, G.4
Charvet, J.P.5
Jaquet, P.6
Brue, T.7
Vialettes, B.8
Enjalbert, A.9
-
43
-
-
0035106606
-
Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: Functional and structural correlates
-
(2001)
Mol Endocrinol
, vol.15
, pp. 411-420
-
-
Valette-Kasik, S.1
Pellegrini-Bouiller, I.2
Sampieri, F.3
Gunz, G.4
Diaz, A.5
Radovick, S.6
Enjalbert, A.7
Brue, T.8
|