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Plos One
|
October 3, 2012
Multiple loci associated with renal function in African Americans
Daniel Shriner, Alan Herbert, Ayo P Doumatey, et al.
Nature Methods
|
June 23, 2006
DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays
Gregory E Crawford, Sean Davis, Peter C Scacheri, et al.
Aging and Disease
|
November 21, 2024
Normal Bone Matrix Mineralization but Altered Growth Plate Morphology in the Lmna<sup>G609G/G609G</sup> Mouse Model of Progeria
Stéphane Blouin, Markus A Hartmann, Nadja Fratzl-Zelman, et al.
Aging Cell
|
October 18, 2024
Angiopoietin-2 reverses endothelial cell dysfunction in progeria vasculature
Sahar Vakili, Elizabeth K Izydore, Leonhard Losert, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 9, 2004
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome
Robert D Goldman, Dale K Shumaker, Michael R Erdos, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2023
Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 hours
Caleb M Grenko, Lori L Bonnycastle, Henry J Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 2020
Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups
Maria B Cubria, Sebastian Suarez, Aidin Masoudi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 2005
Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome
Brian C Capell, Michael R Erdos, James P Madigan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 2009
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization
Pekka Taimen, Katrin Pfleghaar, Takeshi Shimi, et al.
Frontiers in Physiology
|
November 21, 2024
Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model
Indeevar Beeram, Maria Belen Cubria, Pramod Kamalapathy, et al.
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of 11
Search research articles
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Showing results (21-30 of 108) with videos related to
Sort By:
Page
of 11
Plos One
|
October 3, 2012
Multiple loci associated with renal function in African Americans
Daniel Shriner, Alan Herbert, Ayo P Doumatey, et al.
Nature Methods
|
June 23, 2006
DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays
Gregory E Crawford, Sean Davis, Peter C Scacheri, et al.
Aging and Disease
|
November 21, 2024
Normal Bone Matrix Mineralization but Altered Growth Plate Morphology in the Lmna<sup>G609G/G609G</sup> Mouse Model of Progeria
Stéphane Blouin, Markus A Hartmann, Nadja Fratzl-Zelman, et al.
Aging Cell
|
October 18, 2024
Angiopoietin-2 reverses endothelial cell dysfunction in progeria vasculature
Sahar Vakili, Elizabeth K Izydore, Leonhard Losert, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 9, 2004
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome
Robert D Goldman, Dale K Shumaker, Michael R Erdos, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2023
Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 hours
Caleb M Grenko, Lori L Bonnycastle, Henry J Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 2020
Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups
Maria B Cubria, Sebastian Suarez, Aidin Masoudi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 2005
Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome
Brian C Capell, Michael R Erdos, James P Madigan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 2009
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization
Pekka Taimen, Katrin Pfleghaar, Takeshi Shimi, et al.
Frontiers in Physiology
|
November 21, 2024
Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model
Indeevar Beeram, Maria Belen Cubria, Pramod Kamalapathy, et al.
Page
of 11