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Cell Stem Cell
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September 30, 2020
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia
Alfredo Rodríguez, Kaiyang Zhang, Anniina Färkkilä, et al.
Nature Genetics
|
November 5, 2002
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
Karen M Lower, Gillian Turner, Bronwyn A Kerr, et al.
Science Translational Medicine
|
July 29, 2016
Curative ex vivo liver-directed gene therapy in a pig model of hereditary tyrosinemia type 1
Raymond D Hickey, Shennen A Mao, Jaime Glorioso, et al.
American Journal of Human Genetics
|
December 2, 2019
Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction
Julia Wang, Justine Rousseau, Emily Kim, et al.
Immunity
|
November 5, 2013
Anthracyclines induce DNA damage response-mediated protection against severe sepsis
Nuno Figueiredo, Angelo Chora, Helena Raquel, et al.
Med (New York, N.Y.)
|
April 15, 2023
The DNA methylome of human vascular endothelium and its use in liquid biopsies
Ayelet Peretz, Netanel Loyfer, Sheina Piyanzin, et al.
Human Mutation
|
July 12, 2016
Silent Tyrosinemia Type I Without Elevated Tyrosine or Succinylacetone Associated with Liver Cirrhosis and Hepatocellular Carcinoma
Patrick R Blackburn, Raymond D Hickey, Rebecca A Nace, et al.
Cell Reports
|
September 14, 2022
Human hepatocyte PNPLA3-148M exacerbates rapid non-alcoholic fatty liver disease development in chimeric mice
Mohammad Kabbani, Eleftherios Michailidis, Sandra Steensels, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 16, 2016
Identification of tissue-specific cell death using methylation patterns of circulating DNA
Roni Lehmann-Werman, Daniel Neiman, Hai Zemmour, et al.
Blood Advances
|
May 2, 2022
Metformin for treatment of cytopenias in children and young adults with Fanconi anemia
Jessica A Pollard, Elissa Furutani, Shanshan Liu, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 203) with videos related to
Sort By:
Page
of 21
Cell Stem Cell
|
September 30, 2020
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia
Alfredo Rodríguez, Kaiyang Zhang, Anniina Färkkilä, et al.
Nature Genetics
|
November 5, 2002
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
Karen M Lower, Gillian Turner, Bronwyn A Kerr, et al.
Science Translational Medicine
|
July 29, 2016
Curative ex vivo liver-directed gene therapy in a pig model of hereditary tyrosinemia type 1
Raymond D Hickey, Shennen A Mao, Jaime Glorioso, et al.
American Journal of Human Genetics
|
December 2, 2019
Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction
Julia Wang, Justine Rousseau, Emily Kim, et al.
Immunity
|
November 5, 2013
Anthracyclines induce DNA damage response-mediated protection against severe sepsis
Nuno Figueiredo, Angelo Chora, Helena Raquel, et al.
Med (New York, N.Y.)
|
April 15, 2023
The DNA methylome of human vascular endothelium and its use in liquid biopsies
Ayelet Peretz, Netanel Loyfer, Sheina Piyanzin, et al.
Human Mutation
|
July 12, 2016
Silent Tyrosinemia Type I Without Elevated Tyrosine or Succinylacetone Associated with Liver Cirrhosis and Hepatocellular Carcinoma
Patrick R Blackburn, Raymond D Hickey, Rebecca A Nace, et al.
Cell Reports
|
September 14, 2022
Human hepatocyte PNPLA3-148M exacerbates rapid non-alcoholic fatty liver disease development in chimeric mice
Mohammad Kabbani, Eleftherios Michailidis, Sandra Steensels, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 16, 2016
Identification of tissue-specific cell death using methylation patterns of circulating DNA
Roni Lehmann-Werman, Daniel Neiman, Hai Zemmour, et al.
Blood Advances
|
May 2, 2022
Metformin for treatment of cytopenias in children and young adults with Fanconi anemia
Jessica A Pollard, Elissa Furutani, Shanshan Liu, et al.
Page
of 21