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Nature Genetics
|
January 13, 2009
Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism
Frank Rutsch, Susann Gailus, Isabelle R Miousse, et al.
Human Genetics
|
November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly
Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
Journal for Immunotherapy of Cancer
|
September 24, 2025
Tertiary lymphoid structures in Merkel cell carcinoma facilitate naïve and central memory T-cell infiltration linked to immunotherapy response
Nalini Srinivas, Ivelina Spassova, Kuan Cheok Lei, et al.
American Journal of Preventive Cardiology
|
June 15, 2026
Potential impact on cholesterol goal achievement and predicted cardiovascular risk by the addition of ezetimibe and bempedoic acid on top of statins: a simulation from the SANTORINI study
Kausik K Ray, Carlos Aguiar, Marcello Arca, et al.
Cardiovascular Research
|
October 17, 2017
CD40L controls obesity-associated vascular inflammation, oxidative stress, and endothelial dysfunction in high fat diet-treated and db/db mice
Sebastian Steven, Mobin Dib, Michael Hausding, et al.
European Journal of Haematology
|
February 19, 2024
Noninvasive minimal residual disease assessment in relapsed/refractory large B-cell lymphoma using digital droplet PCR
Jan-Michel Heger, Yannick d'Hargues, Fanni Kleinert, et al.
Journal of Medicinal Chemistry
|
September 15, 2020
Targeting Her2-insYVMA with Covalent Inhibitors-A Focused Compound Screening and Structure-Based Design Approach
Jonas Lategahn, Julia Hardick, Tobias Grabe, et al.
ESC Heart Failure
|
December 1, 2021
NT-proBNP as a marker for atrial fibrillation and heart failure in four observational outpatient trials
Stefanie M Werhahn, Christian Becker, Meinhard Mende, et al.
Gastroenterology
|
August 30, 2008
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2
Andre Franke, Annegret Fischer, Michael Nothnagel, et al.
American Journal of Human Genetics
|
April 17, 2007
Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1
Laura Crisponi, Giangiorgio Crisponi, Alessandra Meloni, et al.
Page
of 30
Search research articles
Search
Showing results (241-250 of 296) with videos related to
Sort By:
Page
of 30
Nature Genetics
|
January 13, 2009
Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism
Frank Rutsch, Susann Gailus, Isabelle R Miousse, et al.
Human Genetics
|
November 29, 2005
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly
Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.
Journal for Immunotherapy of Cancer
|
September 24, 2025
Tertiary lymphoid structures in Merkel cell carcinoma facilitate naïve and central memory T-cell infiltration linked to immunotherapy response
Nalini Srinivas, Ivelina Spassova, Kuan Cheok Lei, et al.
American Journal of Preventive Cardiology
|
June 15, 2026
Potential impact on cholesterol goal achievement and predicted cardiovascular risk by the addition of ezetimibe and bempedoic acid on top of statins: a simulation from the SANTORINI study
Kausik K Ray, Carlos Aguiar, Marcello Arca, et al.
Cardiovascular Research
|
October 17, 2017
CD40L controls obesity-associated vascular inflammation, oxidative stress, and endothelial dysfunction in high fat diet-treated and db/db mice
Sebastian Steven, Mobin Dib, Michael Hausding, et al.
European Journal of Haematology
|
February 19, 2024
Noninvasive minimal residual disease assessment in relapsed/refractory large B-cell lymphoma using digital droplet PCR
Jan-Michel Heger, Yannick d'Hargues, Fanni Kleinert, et al.
Journal of Medicinal Chemistry
|
September 15, 2020
Targeting Her2-insYVMA with Covalent Inhibitors-A Focused Compound Screening and Structure-Based Design Approach
Jonas Lategahn, Julia Hardick, Tobias Grabe, et al.
ESC Heart Failure
|
December 1, 2021
NT-proBNP as a marker for atrial fibrillation and heart failure in four observational outpatient trials
Stefanie M Werhahn, Christian Becker, Meinhard Mende, et al.
Gastroenterology
|
August 30, 2008
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2
Andre Franke, Annegret Fischer, Michael Nothnagel, et al.
American Journal of Human Genetics
|
April 17, 2007
Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1
Laura Crisponi, Giangiorgio Crisponi, Alessandra Meloni, et al.
Page
of 30