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Proceedings of the National Academy of Sciences of the United States of America
|
April 26, 2019
Human skin long noncoding RNA WAKMAR1 regulates wound healing by enhancing keratinocyte migration
Dongqing Li, Lara Kular, Manika Vij, et al.
Plos Genetics
|
March 4, 2014
Natural polymorphisms in Tap2 influence negative selection and CD4∶CD8 lineage commitment in the rat
Jonatan Tuncel, Sabrina Haag, Anthony C Y Yau, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 6, 2018
Local Delivery of miR-21 Stabilizes Fibrous Caps in Vulnerable Atherosclerotic Lesions
Hong Jin, Daniel Y Li, Ekaterina Chernogubova, et al.
The Journal of Clinical Investigation
|
November 15, 2019
C-type lectin receptors Mcl and Mincle control development of multiple sclerosis-like neuroinflammation
Marie N'diaye, Susanna Brauner, Sevasti Flytzani, et al.
Journal of Neurology
|
September 12, 2024
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study
Ferdinando Clarelli, Andrea Corona, Kimmo Pääkkönen, et al.
International Journal of Molecular Sciences
|
August 26, 2023
DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes
Alexandre Xavier, Vicki E Maltby, Ewoud Ewing, et al.
Nature Neuroscience
|
March 20, 2026
Single-nucleus epigenomic profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Mukund Kabbe, Eneritz Agirre, Karl E Carlström, et al.
Human Molecular Genetics
|
June 11, 2008
Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer
Yoko Ito, Thibaud Koessler, Ashraf E K Ibrahim, et al.
Cell Reports. Medicine
|
March 19, 2025
T-bet+ CXCR3+ B cells drive hyperreactive B-T cell interactions in multiple sclerosis
Ivan Jelcic, Reza Naghavian, Imran Fanaswala, et al.
Nature Communications
|
July 30, 2024
A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis
Majid Pahlevan Kakhki, Antonino Giordano, Chiara Starvaggi Cucuzza, et al.
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of 11
Search research articles
Search
Showing results (91-100 of 110) with videos related to
Sort By:
Page
of 11
Proceedings of the National Academy of Sciences of the United States of America
|
April 26, 2019
Human skin long noncoding RNA WAKMAR1 regulates wound healing by enhancing keratinocyte migration
Dongqing Li, Lara Kular, Manika Vij, et al.
Plos Genetics
|
March 4, 2014
Natural polymorphisms in Tap2 influence negative selection and CD4∶CD8 lineage commitment in the rat
Jonatan Tuncel, Sabrina Haag, Anthony C Y Yau, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 6, 2018
Local Delivery of miR-21 Stabilizes Fibrous Caps in Vulnerable Atherosclerotic Lesions
Hong Jin, Daniel Y Li, Ekaterina Chernogubova, et al.
The Journal of Clinical Investigation
|
November 15, 2019
C-type lectin receptors Mcl and Mincle control development of multiple sclerosis-like neuroinflammation
Marie N'diaye, Susanna Brauner, Sevasti Flytzani, et al.
Journal of Neurology
|
September 12, 2024
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study
Ferdinando Clarelli, Andrea Corona, Kimmo Pääkkönen, et al.
International Journal of Molecular Sciences
|
August 26, 2023
DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes
Alexandre Xavier, Vicki E Maltby, Ewoud Ewing, et al.
Nature Neuroscience
|
March 20, 2026
Single-nucleus epigenomic profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Mukund Kabbe, Eneritz Agirre, Karl E Carlström, et al.
Human Molecular Genetics
|
June 11, 2008
Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer
Yoko Ito, Thibaud Koessler, Ashraf E K Ibrahim, et al.
Cell Reports. Medicine
|
March 19, 2025
T-bet+ CXCR3+ B cells drive hyperreactive B-T cell interactions in multiple sclerosis
Ivan Jelcic, Reza Naghavian, Imran Fanaswala, et al.
Nature Communications
|
July 30, 2024
A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis
Majid Pahlevan Kakhki, Antonino Giordano, Chiara Starvaggi Cucuzza, et al.
Page
of 11