Accès gratuit
Med Sci (Paris)
Volume 17, Numéro 11, Novembre 2001
Page(s) 1203 - 1207
Section Nouvelles
Publié en ligne 15 novembre 2001
  1. Burrows HL, Douglas KR, Seasholtz AF, Camper SA. Genealogy of the anterior pituitary gland : tracing a family tree. Trends Endocrinol Metab 1999; 10 : 343–52.
  2. Lamonerie T, Tremblay JJ, Lanctôt C, et al. PTX1, a bicoid-related homeobox transcription factor involved in transcription of pro-opiomelanocortin (POMC) gene. Genes Dev 1996; 10 : 1284–95.
  3. Poulin G, Turgeon B, Drouin J. NeuroD1/BETA2 contributes to cell-specific transcription of the POMC gene. Mol Cell Biol 1997; 17 : 6673–82.
  4. Poulin G, Lebel M, Chamberland M, Paradis FW, Drouin J. Specific protein : protein interaction between basic helix-loophelix transcription factors and homeoproteins of the Pitx family. Mol Cell Biol 2000; 20 : 4826–37.
  5. Lanctôt C, Gauthier Y, Drouin J. Pituitary homeobox 1 (Ptx1) is differentially expressed during pituitary development. Endocrinology 1999; 140 : 1416–22.
  6. Lamolet B, Pulichino AM, Lamonerie T, et al. A pituitary cell-restricted T-box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins. Cell 2001; 104 : 849–59.
  7. Smith J. T-box genes: what they do and how they do it. Trends Genet 1999; 15 : 154–8.
  8. Szabo SJ, Kim ST, Costa GL, et al. A novel transcription factor, T-bet, directs Th1 lineage commitment. Cell 2000; 100: 655–69.
  9. Smith J. Brachyury and the T-box genes. Curr Genet Dev 1997; 7 : 474–80.
  10. Dobrovolskaïa-Zavadskaa N. Sur la mortification spontanée de la queue chez la souris nouveau-née et sur l’existence d’un caractère héréditaire « non viable ». CR Soc Biol 1927; 97: 114–6.
  11. Chesley P. Development or the short-tailed mutant in the house mouse. J Exp Zool 1935; 70: 429–59.
  12. Gluecksohn-Schoenheimer S. The development of two tailless mutants in the house mouse. Genetics 1938; 23: 573–84.
  13. Gruneberg H. Genetical studies on the skeleton of the mouse. XXIII. The development of Brachyury and Anury. J embryol Exp Morph 1958; 6 : 424–43.
  14. Herrmann BG, Labeit S, Poustka A, King TR, Lehrach H. Cloning of the T gene required in mesoderm formation in the mouse. Nature 1990; 343 : 617–22.
  15. Merscher S, Funke B, Epstein JA, et al. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge Syndrome. Cell 2001; 104 : 619–29.
  16. Lindsay EA, Vitelli F, Su H, et al. Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 2001; 410 : 97–101.
  17. Bamshad M, Le T, Watkins WS, et al. The spectrum of mutations in TBX3 : tenotype/phenotype relationship in ulnar-mammary syndrome. Am J Hum Genet (Chicago) 1999; 64 : 1550–62.
  18. Basson CT, Bachinsky DR, Lin RC, et al. Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome. Nat Genet 1997; 15 : 30–5.
  19. Li QY, Newbury-Ecob RA, Terrett JA, et al. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Nat Genet 1997; 15 : 21–9.
  20. Kendall SK, Gordon DF, Birkmeier TS, et al. Enhancer-mediated high level expression of mouse pituitary glycoprotein hormone alpha-subunit transgene in thyrotropes, gonadotropes, and developing pituitary gland. Mol Endocrinol 1994; 8 : 1420–33.
  21. Nemeskéri A, Sétalo G, Halasz B. Ontogenesis of the three parts of the fetal rat adenohypophysis. Neuroendocrinology 1988; 48 : 534–43.
  22. Lin SC, 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.
  23. Krude H, Biebermann H, Luck W, et al. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nat Genet 1998; 19 : 155–7.
  24. Malpuech G, Vanlieferinghen P, Dechelotte P, et al. Isolated familial adrenocorticotropin deficiency : prenatal diagnosis by maternal plasma estriol assay. Am J Med Genet 1988; 29 : 125–30.
  25. Kyllo JH, Collins MM, Vetter KL, et al. Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms. Am J Med Genet 1996; 62 : 262–7.
  26. Soo SC, Bain M, Gibson S, et al. Isolated congenital ACTH deficiency : a cleavage enzyme defect? Clin Endocrinol 1994; 40 : 555–6.
  27. Ericson J, Norlin S, Jessell TM, Edlund T. Integrated FGF and BMP signaling controls the progression of progenitor cell differentiation and the emergence of pattern in the embryonic anterior pituitary. Development 1998; 125 : 1005–15.
  28. Treier M, Gleiberman AS, O’Connell SM, et al. Multistep signaling requirements for pituitary organogenesis in vivo. Genes Dev 1998; 12 : 1691–704.
  29. Jacobs JJ, Keblusek P, Robanus-Maandag E, et al. Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19(ARF)) and is amplified in a subset of human breast cancers. Nat Genet 2000; 26 : 291–9.
  30. Chapman DL, Papaioannou VE. Three neural tubes in mouse embryos with mutations in the T-box gene Tbx6. Nature 1998; 391 : 695–7.

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