Ben-Asher E - Search Results

1

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

2

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.

3

The RUNX3 gene--sequence, structure and regulated expression.

Bangsow C, Rubins N, Glusman G, Bernstein Y, Negreanu V, Goldenberg D, Lotem J, Ben-Asher E, Lancet D, Levanon D, Groner Y. Bangsow C, et al. Gene. 2001 Nov 28;279(2):221-32. doi: 10.1016/s0378-1119(01)00760-0. Gene. 2001. PMID: 11733147

4

Identification of the gene causing mucolipidosis type IV.

Bargal R, Avidan N, Ben-Asher E, Olender Z, Zeigler M, Frumkin A, Raas-Rothschild A, Glusman G, Lancet D, Bach G. Bargal R, et al. Nat Genet. 2000 Sep;26(1):118-23. doi: 10.1038/79095. Nat Genet. 2000. PMID: 10973263

5

Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1.

Levanon D, Glusman G, Bangsow T, Ben-Asher E, Male DA, Avidan N, Bangsow C, Hattori M, Taylor TD, Taudien S, Blechschmidt K, Shimizu N, Rosenthal A, Sakaki Y, Lancet D, Groner Y. Levanon D, et al. Gene. 2001 Jan 10;262(1-2):23-33. doi: 10.1016/s0378-1119(00)00532-1. Gene. 2001. PMID: 11179664

6

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.

7

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.

8

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.

9

Harvesting the human genome: the Israeli perspective.

Ben-Asher E, Chalifa-Caspi V, Horn-Saban S, Avidan N, Olender Z, Adato A, Glusman G, Safran M, Rubinstein M, Lancet D. Ben-Asher E, et al. Isr Med Assoc J. 2000 Sep;2(9):657-64. Isr Med Assoc J. 2000. PMID: 11062763 Free article.

10

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.

Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M, Segman RH, Maier W, Macciardi F, Beckmann JS, Lancet D, Lerer B. Amann-Zalcenstein D, et al. Eur J Hum Genet. 2006 Oct;14(10):1111-9. doi: 10.1038/sj.ejhg.5201675. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773125

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