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The Journal of Clinical Investigation|June 4, 2013
MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growthYael Nemlich, Eyal Greenberg, Rona Ortenberg, et al.Journal of the Neurological Sciences|July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world settingNoga Lempel, Shahar Shelly, Odelia Chorin, et al.American Journal of Human Genetics|January 10, 2012
Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1Lina Basel-Vanagaite, Noam Zevit, Adi Har Zahav, et al.American Journal of Human Genetics|November 2, 2010
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic systemEfrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.Nature Cell Biology|July 24, 2007
A reciprocal tensin-3-cten switch mediates EGF-driven mammary cell migrationMenachem Katz, Ido Amit, Ami Citri, et al.Blood|December 8, 2009
Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study GroupLibi Hertzberg, Elena Vendramini, Ithamar Ganmore, et al.The Journal of Experimental Medicine|November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defectsAtar Lev, Yu Nee Lee, Guangping Sun, et al.Frontiers in Genetics|January 26, 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disordersMaayan Kagan, Rotem Semo-Oz, Yishay Ben Moshe, et al.Journal of Medical Genetics|July 3, 2021
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defectsYoav Bolkier, Ortal Barel, Dina Marek-Yagel, et al.The Journal of Experimental Medicine|July 20, 2016
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsAmos J Simon, Atar Lev, Yong Zhang, et al.Pageof 31