Ben-Asher E - Search Results

1

Personal receptor repertoires: olfaction as a model.

Olender T, Waszak SM, Viavant M, Khen M, Ben-Asher E, Reyes A, Nativ N, Wysocki CJ, Ge D, Lancet D. Olender T, et al. Among authors: ben asher e. BMC Genomics. 2012 Aug 21;13:414. doi: 10.1186/1471-2164-13-414. BMC Genomics. 2012. PMID: 22908908 Free PMC article.

2

General olfactory sensitivity database (GOSdb): candidate genes and their genomic variations.

Keydar I, Ben-Asher E, Feldmesser E, Nativ N, Oshimoto A, Restrepo D, Matsunami H, Chien MS, Pinto JM, Gilad Y, Olender T, Lancet D. Keydar I, et al. Among authors: ben asher e. Hum Mutat. 2013 Jan;34(1):32-41. doi: 10.1002/humu.22212. Epub 2012 Oct 11. Hum Mutat. 2013. PMID: 22936402 Free PMC article.

3

Sequence, structure, and evolution of a complete human olfactory receptor gene cluster.

Glusman G, Sosinsky A, Ben-Asher E, Avidan N, Sonkin D, Bahar A, Rosenthal A, Clifton S, Roe B, Ferraz C, Demaille J, Lancet D. Glusman G, et al. Genomics. 2000 Jan 15;63(2):227-45. doi: 10.1006/geno.1999.6030. Genomics. 2000. PMID: 10673334

4

5-Lipoxygenase activating protein (ALOX5AP): association with cardiovascular infarction and stroke.

Ben-Asher E, Lancet D. Ben-Asher E, et al. Isr Med Assoc J. 2004 May;6(5):318-9. Isr Med Assoc J. 2004. PMID: 15151378 Free article. No abstract available.

5

A new gene for the Charcot-Marie-Tooth disorder.

Ben-Asher E, Lancet D. Ben-Asher E, et al. Isr Med Assoc J. 2004 Jun;6(6):376-7. Isr Med Assoc J. 2004. PMID: 15214472 Free article. No abstract available.

6

NIPBL gene responsible for Cornelia de Lange syndrome, a severe developmental disorder.

Ben-Asher E, Lancet D. Ben-Asher E, et al. Isr Med Assoc J. 2004 Sep;6(9):571-2. Isr Med Assoc J. 2004. PMID: 15373324 Free article. No abstract available.

7

LEMD3: the gene responsible for bone density disorders (osteopoikilosis).

Ben-Asher E, Zelzer E, Lancet D. Ben-Asher E, et al. Isr Med Assoc J. 2005 Apr;7(4):273-4. Isr Med Assoc J. 2005. PMID: 15847215 Free article. Review. No abstract available.

8

Association of the RGS2 gene with extrapyramidal symptoms induced by treatment with antipsychotic medication.

Greenbaum L, Strous RD, Kanyas K, Merbl Y, Horowitz A, Karni O, Katz E, Kotler M, Olender T, Deshpande SN, Lancet D, Ben-Asher E, Lerer B. Greenbaum L, et al. Pharmacogenet Genomics. 2007 Jul;17(7):519-28. doi: 10.1097/FPC.0b013e32800ffbb4. Pharmacogenet Genomics. 2007. PMID: 17558307

9

Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis.

Oz-Levi D, Ben-Zeev B, Ruzzo EK, Hitomi Y, Gelman A, Pelak K, Anikster Y, Reznik-Wolf H, Bar-Joseph I, Olender T, Alkelai A, Weiss M, Ben-Asher E, Ge D, Shianna KV, Elazar Z, Goldstein DB, Pras E, Lancet D. Oz-Levi D, et al. Among authors: ben asher e. Am J Hum Genet. 2012 Dec 7;91(6):1065-72. doi: 10.1016/j.ajhg.2012.09.015. Epub 2012 Nov 21. Am J Hum Genet. 2012. PMID: 23176824 Free PMC article.

10

Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.

Vodo D, Sarig O, Geller S, Ben-Asher E, Olender T, Bochner R, Goldberg I, Nosgorodsky J, Alkelai A, Tatarskyy P, Peled A, Baum S, Barzilai A, Ibrahim SM, Zillikens D, Lancet D, Sprecher E. Vodo D, et al. Among authors: ben asher e. PLoS Genet. 2016 May 5;12(5):e1006008. doi: 10.1371/journal.pgen.1006008. eCollection 2016 May. PLoS Genet. 2016. PMID: 27148741 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

57 results

Search Page