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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1982 1
1984 1
1988 1
1989 1
1991 1
1993 1
1994 1
1995 2
2000 3
2001 5
2002 2
2003 2
2004 5
2005 2
2006 5
2007 7
2008 4
2009 2
2010 3
2011 2
2012 5
2013 2
2016 1
2022 1
2023 1
2024 1

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57 results

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Page 1
Interpersonal Family Dynamics Relate to Hippocampal CA Subfield Structure.
Coughlin C, Ben-Asher E, Roome HE, Varga NL, Moreau MM, Schneider LL, Preston AR. Coughlin C, et al. Among authors: ben asher e. Front Neurosci. 2022 Jun 17;16:872101. doi: 10.3389/fnins.2022.872101. eCollection 2022. Front Neurosci. 2022. PMID: 35784846 Free PMC article.
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.
Transcription termination in animal viruses and cells.
Resnekov O, Ben-Asher E, Bengal E, Choder M, Hay N, Kessler M, Ragimov N, Seiberg M, Skolnik-David H, Aloni Y. Resnekov O, et al. Among authors: ben asher e. Gene. 1988 Dec 10;72(1-2):91-104. doi: 10.1016/0378-1119(88)90130-8. Gene. 1988. PMID: 2854091
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.
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. Among authors: ben asher e. Gene. 2001 Nov 28;279(2):221-32. doi: 10.1016/s0378-1119(01)00760-0. Gene. 2001. PMID: 11733147
CATSPER2, a human autosomal nonsyndromic male infertility gene.
Avidan N, Tamary H, Dgany O, Cattan D, Pariente A, Thulliez M, Borot N, Moati L, Barthelme A, Shalmon L, Krasnov T, Ben-Asher E, Olender T, Khen M, Yaniv I, Zaizov R, Shalev H, Delaunay J, Fellous M, Lancet D, Beckmann JS. Avidan N, et al. Among authors: ben asher e. Eur J Hum Genet. 2003 Jul;11(7):497-502. doi: 10.1038/sj.ejhg.5200991. Eur J Hum Genet. 2003. PMID: 12825070
Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy.
Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, Colleaux L, Décarie JC, Blaser S, Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ME, Aryal DK, Rodriguiz RM, Jiang YH, Wetsel WC, McNamara JO, Rouleau GA, Silver DL, Lancet D, Pras E, Mitchell GA, Michaud JL, Goldstein DB. Ruzzo EK, et al. Among authors: ben asher e. Neuron. 2013 Oct 16;80(2):429-41. doi: 10.1016/j.neuron.2013.08.013. Neuron. 2013. PMID: 24139043 Free PMC article.
57 results