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Biorxiv : the Preprint Server for Biology
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April 17, 2026
Competing forms of protein-protein association and DNA binding exhibited by BrxC from the BREX phage restriction system
Alex J Kaiser, Jenny J Readshaw, Lindsey A Doyle, et al.
Journal of the American Society of Nephrology : JASN
|
March 15, 2019
The RNA-Protein Interactome of Differentiated Kidney Tubular Epithelial Cells
Michael Ignarski, Constantin Rill, Rainer W J Kaiser, et al.
Brain : a Journal of Neurology
|
April 28, 2022
Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onset
Joanne Trinh, Theresa Lüth, Susen Schaake, et al.
Circulation
|
May 11, 2017
Functional Characterization of the <i>GUCY1A3</i> Coronary Artery Disease Risk Locus
Thorsten Kessler, Jana Wobst, Bernhard Wolf, et al.
Nature Genetics
|
February 26, 2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
Sheila Unger, Detlef Böhm, Frank J Kaiser, et al.
Journal of Medical Genetics
|
October 2, 2015
HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome
Ronja Hollstein, David A Parry, Lisa Nalbach, et al.
BMC Medical Education
|
October 12, 2018
The Next Generation Scientist program: capacity-building for future scientific leaders in low- and middle-income countries
Goonaseelan Pillai, Kelly Chibale, Edwin C Constable, et al.
Optics Letters
|
September 12, 2009
Dynamically stable 0 degrees phase mode operation of a grating-surface-emitting diode-laser array
N W Carlson, G A Evans, J M Hammer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 7, 2014
Caspase-8 and RIP kinases regulate bacteria-induced innate immune responses and cell death
Dan Weng, Robyn Marty-Roix, Sandhya Ganesan, et al.
International Journal of Molecular Sciences
|
June 12, 2014
Functional characterization of NIPBL physiological splice variants and eight splicing mutations in patients with Cornelia de Lange syndrome
María E Teresa-Rodrigo, Juliane Eckhold, Beatriz Puisac, et al.
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of 63
Search research articles
Search
Showing results (551-560 of 621) with videos related to
Sort By:
Page
of 63
Biorxiv : the Preprint Server for Biology
|
April 17, 2026
Competing forms of protein-protein association and DNA binding exhibited by BrxC from the BREX phage restriction system
Alex J Kaiser, Jenny J Readshaw, Lindsey A Doyle, et al.
Journal of the American Society of Nephrology : JASN
|
March 15, 2019
The RNA-Protein Interactome of Differentiated Kidney Tubular Epithelial Cells
Michael Ignarski, Constantin Rill, Rainer W J Kaiser, et al.
Brain : a Journal of Neurology
|
April 28, 2022
Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onset
Joanne Trinh, Theresa Lüth, Susen Schaake, et al.
Circulation
|
May 11, 2017
Functional Characterization of the <i>GUCY1A3</i> Coronary Artery Disease Risk Locus
Thorsten Kessler, Jana Wobst, Bernhard Wolf, et al.
Nature Genetics
|
February 26, 2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
Sheila Unger, Detlef Böhm, Frank J Kaiser, et al.
Journal of Medical Genetics
|
October 2, 2015
HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome
Ronja Hollstein, David A Parry, Lisa Nalbach, et al.
BMC Medical Education
|
October 12, 2018
The Next Generation Scientist program: capacity-building for future scientific leaders in low- and middle-income countries
Goonaseelan Pillai, Kelly Chibale, Edwin C Constable, et al.
Optics Letters
|
September 12, 2009
Dynamically stable 0 degrees phase mode operation of a grating-surface-emitting diode-laser array
N W Carlson, G A Evans, J M Hammer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 7, 2014
Caspase-8 and RIP kinases regulate bacteria-induced innate immune responses and cell death
Dan Weng, Robyn Marty-Roix, Sandhya Ganesan, et al.
International Journal of Molecular Sciences
|
June 12, 2014
Functional characterization of NIPBL physiological splice variants and eight splicing mutations in patients with Cornelia de Lange syndrome
María E Teresa-Rodrigo, Juliane Eckhold, Beatriz Puisac, et al.
Page
of 63