Arafat M - Search Results

1

A novel role for nucleolin in splice site selection.

Shefer K, Boulos A, Gotea V, Arafat M, Ben Chaim Y, Muharram A, Isaac S, Eden A, Sperling J, Elnitski L, Sperling R. Shefer K, et al. Among authors: arafat m. RNA Biol. 2022;19(1):333-352. doi: 10.1080/15476286.2021.2020455. Epub 2021 Dec 31. RNA Biol. 2022. PMID: 35220879 Free PMC article.

2

A Quality Control Mechanism of Splice Site Selection Abrogated under Stress and in Cancer.

Arafat M, Sperling R. Arafat M, et al. Cancers (Basel). 2022 Mar 30;14(7):1750. doi: 10.3390/cancers14071750. Cancers (Basel). 2022. PMID: 35406522 Free PMC article. Review.

3

Crosstalk between Long Non-Coding RNA and Spliceosomal microRNA as a Novel Biomarker for Cancer.

Arafat M, Sperling R. Arafat M, et al. Noncoding RNA. 2023 Jul 31;9(4):42. doi: 10.3390/ncrna9040042. Noncoding RNA. 2023. PMID: 37624034 Free PMC article. Review.

4

A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy.

Levitas A, Muhammad E, Zhang Y, Perea Gil I, Serrano R, Diaz N, Arafat M, Gavidia AA, Kapiloff MS, Mercola M, Etzion Y, Parvari R, Karakikes I. Levitas A, et al. Among authors: arafat m. PLoS Genet. 2020 Sep 14;16(9):e1009000. doi: 10.1371/journal.pgen.1009000. eCollection 2020 Sep. PLoS Genet. 2020. PMID: 32925938 Free PMC article.

5

Combined adrenal failure and testicular adrenal rest tumor in a patient with nicotinamide nucleotide transhydrogenase deficiency.

Hershkovitz E, Arafat M, Loewenthal N, Haim A, Parvari R. Hershkovitz E, et al. Among authors: arafat m. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1187-90. doi: 10.1515/jpem-2015-0075. J Pediatr Endocrinol Metab. 2015. PMID: 25879317

6

Mutation in TDRD9 causes non-obstructive azoospermia in infertile men.

Arafat M, Har-Vardi I, Harlev A, Levitas E, Zeadna A, Abofoul-Azab M, Dyomin V, Sheffield VC, Lunenfeld E, Huleihel M, Parvari R. Arafat M, et al. J Med Genet. 2017 Sep;54(9):633-639. doi: 10.1136/jmedgenet-2017-104514. Epub 2017 May 23. J Med Genet. 2017. PMID: 28536242

7

Congenital thrombotic thrombocytopenic purpura in a large cohort of patients carrying a novel mutation in ADAMTS13 gene.

Pikovsky O, Arafat M, Ovadia H, Sharoni Y, Al-Athamen K, Kanengisser-Pines B, Keren-Politansky A, Levi I, Erez O, Parvari R, Rabinovich A. Pikovsky O, et al. Among authors: arafat m. Thromb Res. 2020 Jan;185:167-170. doi: 10.1016/j.thromres.2019.12.002. Epub 2019 Dec 5. Thromb Res. 2020. PMID: 31837614 No abstract available.

8

Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.

Arafat M, Zeadna A, Levitas E, Har Vardi I, Samueli B, Shaco-Levy R, Dabsan S, Lunenfeld E, Huleihel M, Parvari R. Arafat M, et al. Mol Genet Genomic Med. 2020 Jul;8(7):e1258. doi: 10.1002/mgg3.1258. Epub 2020 May 15. Mol Genet Genomic Med. 2020. PMID: 32410375 Free PMC article.

9

Mutation in CATIP (C2orf62) causes oligoteratoasthenozoospermia by affecting actin dynamics.

Arafat M, Harlev A, Har-Vardi I, Levitas E, Priel T, Gershoni M, Searby C, Sheffield VC, Lunenfeld E, Parvari R. Arafat M, et al. J Med Genet. 2020 Jun 5:jmedgenet-2019-106825. doi: 10.1136/jmedgenet-2019-106825. Online ahead of print. J Med Genet. 2020. PMID: 32503832

10

Pathogenic variations in Germ Cell Nuclear Acidic Peptidase (GCNA) are associated with human male infertility.

Arafat M, Kleiman SE, AbuMadighem A, Zeadna A, Levitas E, Vardi IH, Barda S, Lehavi O, Hauser R, Lunenfeld E, Huleihel M, Gershoni M, Parvari R. Arafat M, et al. Eur J Hum Genet. 2021 Dec;29(12):1781-1788. doi: 10.1038/s41431-021-00946-2. Epub 2021 Aug 20. Eur J Hum Genet. 2021. PMID: 34413498 Free PMC article.

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