Omran H - Search Results

1

Lateralization defects and ciliary dyskinesia: lessons from algae.

El Zein L, Omran H, Bouvagnet P. El Zein L, et al. Among authors: omran h. Trends Genet. 2003 Mar;19(3):162-7. doi: 10.1016/S0168-9525(03)00026-X. Trends Genet. 2003. PMID: 12615011 Review.

2

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.

Olbrich H, Häffner K, Kispert A, Völkel A, Volz A, Sasmaz G, Reinhardt R, Hennig S, Lehrach H, Konietzko N, Zariwala M, Noone PG, Knowles M, Mitchison HM, Meeks M, Chung EM, Hildebrandt F, Sudbrak R, Omran H. Olbrich H, et al. Among authors: omran h. Nat Genet. 2002 Feb;30(2):143-4. doi: 10.1038/ng817. Epub 2002 Jan 14. Nat Genet. 2002. PMID: 11788826

3

Novel tools to unravel molecular mechanisms in cilia-related disorders.

Fliegauf M, Omran H. Fliegauf M, et al. Among authors: omran h. Trends Genet. 2006 May;22(5):241-5. doi: 10.1016/j.tig.2006.03.002. Epub 2006 Mar 24. Trends Genet. 2006. PMID: 16564109 Review.

4

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm.

Loges NT, Olbrich H, Fenske L, Mussaffi H, Horvath J, Fliegauf M, Kuhl H, Baktai G, Peterffy E, Chodhari R, Chung EM, Rutman A, O'Callaghan C, Blau H, Tiszlavicz L, Voelkel K, Witt M, Zietkiewicz E, Neesen J, Reinhardt R, Mitchison HM, Omran H. Loges NT, et al. Among authors: omran h. Am J Hum Genet. 2008 Nov;83(5):547-58. doi: 10.1016/j.ajhg.2008.10.001. Epub 2008 Oct 23. Am J Hum Genet. 2008. PMID: 18950741 Free PMC article.

5

To beat or not to beat: roles of cilia in development and disease.

Ibañez-Tallon I, Heintz N, Omran H. Ibañez-Tallon I, et al. Among authors: omran h. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R27-35. doi: 10.1093/hmg/ddg061. Hum Mol Genet. 2003. PMID: 12668594 Review.

6

Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.

Ibañez-Tallon I, Pagenstecher A, Fliegauf M, Olbrich H, Kispert A, Ketelsen UP, North A, Heintz N, Omran H. Ibañez-Tallon I, et al. Among authors: omran h. Hum Mol Genet. 2004 Sep 15;13(18):2133-41. doi: 10.1093/hmg/ddh219. Epub 2004 Jul 21. Hum Mol Genet. 2004. PMID: 15269178

7

Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics.

Storm van's Gravesande K, Omran H. Storm van's Gravesande K, et al. Among authors: omran h. Ann Med. 2005;37(6):439-49. doi: 10.1080/07853890510011985. Ann Med. 2005. PMID: 16203616 Review.

8

Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia.

Olbrich H, Horváth J, Fekete A, Loges NT, Storm van's Gravesande K, Blum A, Hörmann K, Omran H. Olbrich H, et al. Among authors: omran h. Pediatr Res. 2006 Mar;59(3):418-22. doi: 10.1203/01.pdr.0000200809.21364.e2. Pediatr Res. 2006. PMID: 16492982

9

Genetic defects in ciliary structure and function.

Zariwala MA, Knowles MR, Omran H. Zariwala MA, et al. Among authors: omran h. Annu Rev Physiol. 2007;69:423-50. doi: 10.1146/annurev.physiol.69.040705.141301. Annu Rev Physiol. 2007. PMID: 17059358 Review.

10

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia.

Tan SY, Rosenthal J, Zhao XQ, Francis RJ, Chatterjee B, Sabol SL, Linask KL, Bracero L, Connelly PS, Daniels MP, Yu Q, Omran H, Leatherbury L, Lo CW. Tan SY, et al. Among authors: omran h. J Clin Invest. 2007 Dec;117(12):3742-52. doi: 10.1172/JCI33284. J Clin Invest. 2007. PMID: 18037990 Free PMC article.

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