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K Alder

Showing results (11-20 of 69) with videos related to

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American Journal of Human Genetics|December 1, 2009
Short telomeres are sufficient to cause the degenerative defects associated with agingMary Armanios, Jonathan K Alder, Erin M Parry, et al.
Chest|December 25, 2014
Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosisJonathan K Alder, Susan E Stanley, Christa L Wagner, et al.
Epigenetics|May 21, 2010
Id1 overexpression is independent of repression and epigenetic silencing of tumor suppressor genes in melanomaMegan A Healey, Staci L Deaton, Jonathan K Alder, et al.
The American Journal of Pathology|December 30, 2023
Mammalian Target of Rapamycin Complex 1 Activation in Macrophages Contributes to Persistent Lung Inflammation following Respiratory Tract Viral InfectionBrydie R Huckestein, Kelly Zeng, Rosemary Westcott, et al.
Stem Cells (Dayton, Ohio)|March 4, 2006
HES1 inhibits cycling of hematopoietic progenitor cells via DNA bindingXiaobing Yu, Jonathan K Alder, Jong Ho Chun, et al.
Journal of Medical Genetics|March 19, 2011
Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenitaErin M Parry, Jonathan K Alder, Stella S Lee, et al.
Cell Biology International|February 20, 2018
Comparative analysis of lipid-mediated CRISPR-Cas9 genome editing techniquesKelsey P Ringer, Mark G Roth, Mitchell S Garey, et al.
Springerplus|September 22, 2016
CRISPR-Cas9 directed knock-out of a constitutively expressed gene using lance array nanoinjectionJohn W Sessions, Craig S Skousen, Kevin D Price, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 9, 2008
Kruppel-like factor 4 is essential for inflammatory monocyte differentiation in vivoJonathan K Alder, Robert W Georgantas, Richard L Hildreth, et al.
Human Mutation|August 16, 2013
Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) geneJonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, et al.
Pageof 7

Showing results (11-20 of 69) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|December 1, 2009
Short telomeres are sufficient to cause the degenerative defects associated with agingMary Armanios, Jonathan K Alder, Erin M Parry, et al.
Chest|December 25, 2014
Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosisJonathan K Alder, Susan E Stanley, Christa L Wagner, et al.
Epigenetics|May 21, 2010
Id1 overexpression is independent of repression and epigenetic silencing of tumor suppressor genes in melanomaMegan A Healey, Staci L Deaton, Jonathan K Alder, et al.
The American Journal of Pathology|December 30, 2023
Mammalian Target of Rapamycin Complex 1 Activation in Macrophages Contributes to Persistent Lung Inflammation following Respiratory Tract Viral InfectionBrydie R Huckestein, Kelly Zeng, Rosemary Westcott, et al.
Stem Cells (Dayton, Ohio)|March 4, 2006
HES1 inhibits cycling of hematopoietic progenitor cells via DNA bindingXiaobing Yu, Jonathan K Alder, Jong Ho Chun, et al.
Journal of Medical Genetics|March 19, 2011
Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenitaErin M Parry, Jonathan K Alder, Stella S Lee, et al.
Cell Biology International|February 20, 2018
Comparative analysis of lipid-mediated CRISPR-Cas9 genome editing techniquesKelsey P Ringer, Mark G Roth, Mitchell S Garey, et al.
Springerplus|September 22, 2016
CRISPR-Cas9 directed knock-out of a constitutively expressed gene using lance array nanoinjectionJohn W Sessions, Craig S Skousen, Kevin D Price, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 9, 2008
Kruppel-like factor 4 is essential for inflammatory monocyte differentiation in vivoJonathan K Alder, Robert W Georgantas, Richard L Hildreth, et al.
Human Mutation|August 16, 2013
Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) geneJonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, et al.
Pageof 7