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Angewandte Chemie (International Ed. in English)
|
June 7, 2018
An Unusual Intramolecular Halogen Bond Guides Conformational Selection
Roberta Tesch, Christian Becker, Matthias Philipp Müller, et al.
Molecular Cell
|
May 1, 2018
HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell Types
Anne Zirkel, Milos Nikolic, Konstantinos Sofiadis, et al.
Genome Medicine
|
August 23, 2023
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
Nikolai Tschernoster, Florian Erger, Stefan Kohl, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 20, 2024
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia
Maria Asif, Arwa Ishaq A Khayyat, Salem Alawbathani, et al.
Journal for Immunotherapy of Cancer
|
January 25, 2022
Clinical and molecular characteristics associated with response to therapeutic PD-1/PD-L1 inhibition in advanced Merkel cell carcinoma
Ivelina Spassova, Selma Ugurel, Linda Kubat, et al.
Plos One
|
August 9, 2007
Systematic association mapping identifies NELL1 as a novel IBD disease gene
Andre Franke, Jochen Hampe, Philip Rosenstiel, et al.
American Journal of Human Genetics
|
February 3, 2007
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation
Francesca Pasutto, Heinrich Sticht, Gerhard Hammersen, et al.
American Journal of Human Genetics
|
October 13, 2006
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement
Martin Konrad, Andre Schaller, Dominik Seelow, et al.
Science Immunology
|
August 8, 2017
Constitutive resistance to viral infection in human CD141<sup>+</sup> dendritic cells
Aymeric Silvin, Chun I Yu, Xavier Lahaye, et al.
American Journal of Human Genetics
|
July 19, 2011
Faulty initiation of proteoglycan synthesis causes cardiac and joint defects
Sevjidmaa Baasanjav, Lihadh Al-Gazali, Taishi Hashiguchi, et al.
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of 30
Search research articles
Search
Showing results (251-260 of 296) with videos related to
Sort By:
Page
of 30
Angewandte Chemie (International Ed. in English)
|
June 7, 2018
An Unusual Intramolecular Halogen Bond Guides Conformational Selection
Roberta Tesch, Christian Becker, Matthias Philipp Müller, et al.
Molecular Cell
|
May 1, 2018
HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell Types
Anne Zirkel, Milos Nikolic, Konstantinos Sofiadis, et al.
Genome Medicine
|
August 23, 2023
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
Nikolai Tschernoster, Florian Erger, Stefan Kohl, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 20, 2024
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia
Maria Asif, Arwa Ishaq A Khayyat, Salem Alawbathani, et al.
Journal for Immunotherapy of Cancer
|
January 25, 2022
Clinical and molecular characteristics associated with response to therapeutic PD-1/PD-L1 inhibition in advanced Merkel cell carcinoma
Ivelina Spassova, Selma Ugurel, Linda Kubat, et al.
Plos One
|
August 9, 2007
Systematic association mapping identifies NELL1 as a novel IBD disease gene
Andre Franke, Jochen Hampe, Philip Rosenstiel, et al.
American Journal of Human Genetics
|
February 3, 2007
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation
Francesca Pasutto, Heinrich Sticht, Gerhard Hammersen, et al.
American Journal of Human Genetics
|
October 13, 2006
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement
Martin Konrad, Andre Schaller, Dominik Seelow, et al.
Science Immunology
|
August 8, 2017
Constitutive resistance to viral infection in human CD141<sup>+</sup> dendritic cells
Aymeric Silvin, Chun I Yu, Xavier Lahaye, et al.
American Journal of Human Genetics
|
July 19, 2011
Faulty initiation of proteoglycan synthesis causes cardiac and joint defects
Sevjidmaa Baasanjav, Lihadh Al-Gazali, Taishi Hashiguchi, et al.
Page
of 30