Petit C - Search Results

1

Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis.

Cohen-Salmon M, Regnault B, Cayet N, Caille D, Demuth K, Hardelin JP, Janel N, Meda P, Petit C. Cohen-Salmon M, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6229-34. doi: 10.1073/pnas.0605108104. Epub 2007 Mar 30. Proc Natl Acad Sci U S A. 2007. PMID: 17400755 Free PMC article.

2

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome.

del Castillo I, Cohen-Salmon M, Blanchard S, Lutfalla G, Petit C. del Castillo I, et al. Among authors: petit c. Nat Genet. 1992 Dec;2(4):305-10. doi: 10.1038/ng1292-305. Nat Genet. 1992. PMID: 1303284

3

A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndrome.

Hardelin JP, Petit C. Hardelin JP, et al. Among authors: petit c. Baillieres Clin Endocrinol Metab. 1995 Jul;9(3):489-507. doi: 10.1016/s0950-351x(95)80553-2. Baillieres Clin Endocrinol Metab. 1995. PMID: 7575329 Review.

4

Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome.

Cohen-Salmon M, Tronche F, del Castillo I, Petit C. Cohen-Salmon M, et al. Among authors: petit c. Gene. 1995 Oct 27;164(2):235-42. doi: 10.1016/0378-1119(95)00481-k. Gene. 1995. PMID: 7590336

5

Early expression of the KAL gene during embryonic development of the chick.

Legouis R, Hardelin JP, Petit C, Ayer-Le Lièvre C. Legouis R, et al. Among authors: petit c. Anat Embryol (Berl). 1994 Dec;190(6):549-62. doi: 10.1007/BF00190105. Anat Embryol (Berl). 1994. PMID: 7893008

6

Isolation and characterization of the gene responsible for the X chromosome-linked Kallmann syndrome.

Legouis R, Cohen-Salmon M, Del Castillo I, Petit C. Legouis R, et al. Among authors: petit c. Biomed Pharmacother. 1994;48(5-6):241-6. doi: 10.1016/0753-3322(94)90139-2. Biomed Pharmacother. 1994. PMID: 7999985 Review.

7

Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndrome.

Legouis R, Cohen-Salmon M, del Castillo I, Levilliers J, Capy L, Mornow JP, Petit C. Legouis R, et al. Among authors: petit c. Genomics. 1993 Aug;17(2):516-8. doi: 10.1006/geno.1993.1360. Genomics. 1993. PMID: 8406507

8

Xp22.3 deletions in isolated familial Kallmann's syndrome.

Hardelin JP, Levilliers J, Young J, Pholsena M, Legouis R, Kirk J, Bouloux P, Petit C, Schaison G. Hardelin JP, et al. Among authors: petit c. J Clin Endocrinol Metab. 1993 Apr;76(4):827-31. doi: 10.1210/jcem.76.4.8473391. J Clin Endocrinol Metab. 1993. PMID: 8473391

9

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.

Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C. Hardelin JP, et al. Among authors: petit c. Hum Mol Genet. 1993 Apr;2(4):373-7. doi: 10.1093/hmg/2.4.373. Hum Mol Genet. 1993. PMID: 8504298

10

Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system.

Soussi-Yanicostas N, Hardelin JP, Arroyo-Jimenez MM, Ardouin O, Legouis R, Levilliers J, Traincard F, Betton JM, Cabanié L, Petit C. Soussi-Yanicostas N, et al. Among authors: petit c. J Cell Sci. 1996 Jul;109 ( Pt 7):1749-57. doi: 10.1242/jcs.109.7.1749. J Cell Sci. 1996. PMID: 8832397

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