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2006 1
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2011 1
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17 results

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Page 1
SF3B1 association with chromatin determines splicing outcomes.
Kfir N, Lev-Maor G, Glaich O, Alajem A, Datta A, Sze SK, Meshorer E, Ast G. Kfir N, et al. Cell Rep. 2015 Apr 28;11(4):618-29. doi: 10.1016/j.celrep.2015.03.048. Epub 2015 Apr 16. Cell Rep. 2015. PMID: 25892229 Free article.
Degradation of Bcl-2 by XIAP and ARTS Promotes Apoptosis.
Edison N, Curtz Y, Paland N, Mamriev D, Chorubczyk N, Haviv-Reingewertz T, Kfir N, Morgenstern D, Kupervaser M, Kagan J, Kim HT, Larisch S. Edison N, et al. Among authors: kfir n. Cell Rep. 2017 Oct 10;21(2):442-454. doi: 10.1016/j.celrep.2017.09.052. Cell Rep. 2017. PMID: 29020630 Free PMC article.
High-quality chromosome-scale genomes facilitate effective identification of large structural variations in hot and sweet peppers.
Lee JH, Venkatesh J, Jo J, Jang S, Kim GW, Kim JM, Han K, Ro N, Lee HY, Kwon JK, Kim YM, Lee TH, Choi D, Van Deynze A, Hill T, Kfir N, Freiman A, Davila Olivas NH, Elkind Y, Paran I, Kang BC. Lee JH, et al. Among authors: kfir n. Hortic Res. 2022 Sep 19;9:uhac210. doi: 10.1093/hr/uhac210. eCollection 2022. Hortic Res. 2022. PMID: 36467270 Free PMC article.
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules.
Gunay-Aygun M, Falik-Zaccai TC, Vilboux T, Zivony-Elboum Y, Gumruk F, Cetin M, Khayat M, Boerkoel CF, Kfir N, Huang Y, Maynard D, Dorward H, Berger K, Kleta R, Anikster Y, Arat M, Freiberg AS, Kehrel BE, Jurk K, Cruz P, Mullikin JC, White JG, Huizing M, Gahl WA. Gunay-Aygun M, et al. Among authors: kfir n. Nat Genet. 2011 Jul 17;43(8):732-4. doi: 10.1038/ng.883. Nat Genet. 2011. PMID: 21765412 Free PMC article.
A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis.
Zivony-Elboum Y, Westbroek W, Kfir N, Savitzki D, Shoval Y, Bloom A, Rod R, Khayat M, Gross B, Samri W, Cohen H, Sonkin V, Freidman T, Geiger D, Fattal-Valevski A, Anikster Y, Waters AM, Kleta R, Falik-Zaccai TC. Zivony-Elboum Y, et al. Among authors: kfir n. J Med Genet. 2012 Jul;49(7):462-72. doi: 10.1136/jmedgenet-2012-100742. Epub 2012 Jun 20. J Med Genet. 2012. PMID: 22717650
17 results