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Gideon Rechavi

Showing results (281-290 of 297) with videos related to

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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.
Blood|September 11, 2020
Epigenetic loss of m1A RNA demethylase ALKBH3 in Hodgkin lymphoma targets collagen, conferring poor clinical outcomeRosaura Esteve-Puig, Fina Climent, David Piñeyro, 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.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Science (New York, N.Y.)|January 9, 2015
Stem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiationShay Geula, Sharon Moshitch-Moshkovitz, Dan Dominissini, et al.
Scientific Reports|September 28, 2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomaliesBen Pode-Shakked, Ortal Barel, Amihood Singer, et al.
Pageof 30

Showing results (281-290 of 297) with videos related to

Sort By:
Pageof 30
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.
Blood|September 11, 2020
Epigenetic loss of m1A RNA demethylase ALKBH3 in Hodgkin lymphoma targets collagen, conferring poor clinical outcomeRosaura Esteve-Puig, Fina Climent, David Piñeyro, 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.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Science (New York, N.Y.)|January 9, 2015
Stem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiationShay Geula, Sharon Moshitch-Moshkovitz, Dan Dominissini, et al.
Scientific Reports|September 28, 2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomaliesBen Pode-Shakked, Ortal Barel, Amihood Singer, et al.
Pageof 30