Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

88 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Molecular genetics of hearing loss.
Petit C, Levilliers J, Hardelin JP. Petit C, et al. Among authors: hardelin jp. Annu Rev Genet. 2001;35:589-646. doi: 10.1146/annurev.genet.35.102401.091224. Annu Rev Genet. 2001. PMID: 11700295 Review.
A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndrome.
Hardelin JP, Petit C. Hardelin JP, et al. 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.
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. J Clin Endocrinol Metab. 1993 Apr;76(4):827-31. doi: 10.1210/jcem.76.4.8473391. J Clin Endocrinol Metab. 1993. PMID: 8473391
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. Hum Mol Genet. 1993 Apr;2(4):373-7. doi: 10.1093/hmg/2.4.373. Hum Mol Genet. 1993. PMID: 8504298
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome.
Hardelin JP, Soussi-Yanicostas N, Levilliers J, Kalatzis V, Abdelhak S, Cohen-Salmon M, Petit C. Hardelin JP, et al. Adv Nephrol Necker Hosp. 1998;28:419-28. Adv Nephrol Necker Hosp. 1998. PMID: 9890002 Review. No abstract available.
Unconventional myosin VIIA is a novel A-kinase-anchoring protein.
Küssel-Andermann P, El-Amraoui A, Safieddine S, Hardelin JP, Nouaille S, Camonis J, Petit C. Küssel-Andermann P, et al. Among authors: hardelin jp. J Biol Chem. 2000 Sep 22;275(38):29654-9. doi: 10.1074/jbc.M004393200. J Biol Chem. 2000. PMID: 10889203
Kallmann syndrome: towards molecular pathogenesis.
Hardelin JP. Hardelin JP. Mol Cell Endocrinol. 2001 Jun 20;179(1-2):75-81. doi: 10.1016/s0303-7207(01)00462-2. Mol Cell Endocrinol. 2001. PMID: 11420131 Review.
A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.
Coimbra RS, Weil D, Brottier P, Blanchard S, Levi M, Hardelin JP, Weissenbach J, Petit C. Coimbra RS, et al. Among authors: hardelin jp. Genome Res. 2002 Jun;12(6):1007-11. doi: 10.1101/gr.227502. Genome Res. 2002. PMID: 12045154 Free PMC article.
Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.
Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C. Cohen-Salmon M, et al. Among authors: hardelin jp. Curr Biol. 2002 Jul 9;12(13):1106-11. doi: 10.1016/s0960-9822(02)00904-1. Curr Biol. 2002. PMID: 12121617 Free PMC article.
Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential.
Teubner B, Michel V, Pesch J, Lautermann J, Cohen-Salmon M, Söhl G, Jahnke K, Winterhager E, Herberhold C, Hardelin JP, Petit C, Willecke K. Teubner B, et al. Among authors: hardelin jp. Hum Mol Genet. 2003 Jan 1;12(1):13-21. doi: 10.1093/hmg/ddg001. Hum Mol Genet. 2003. PMID: 12490528
88 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback