Search research articles
Contact Us
Filters
Showing results (561-570 of 577) with videos related to
Page
of 58
Sort By:
Human Molecular Genetics
|
August 14, 2003
An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
W H Irwin McLean, Alan D Irvine, Kevin J Hamill, et al.
Elife
|
January 17, 2015
The contrasting phylodynamics of human influenza B viruses
Dhanasekaran Vijaykrishna, Edward C Holmes, Udayan Joseph, et al.
Nature Genetics
|
April 10, 2007
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
Aileen Sandilands, Ana Terron-Kwiatkowski, Peter R Hull, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 14, 2006
Establishment of multiple sublineages of H5N1 influenza virus in Asia: implications for pandemic control
H Chen, G J D Smith, K S Li, et al.
BMJ Global Health
|
February 6, 2026
Strengthening supply chains for pathogen genomic surveillance in Asia
Anne-Claire Stona, Yoong Khean Khoo, La Moe, et al.
Nature Genetics
|
October 16, 2012
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma
Elizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.
Virus Evolution
|
January 19, 2023
Genomic epidemiology of SARS-CoV-2 in Cambodia, January 2020 to February 2021
Yvonne C F Su, Jordan Z J Ma, Tey Putita Ou, et al.
Lancet (London, England)
|
August 22, 2020
Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
Barnaby E Young, Siew-Wai Fong, Yi-Hao Chan, et al.
Communications Medicine
|
November 28, 2024
Spatiotemporal evolution and transmission dynamics of Alpha and Delta SARS-CoV-2 variants contributing to sequential outbreaks in Cambodia during 2021
Yvonne C F Su, Michael A Zeller, Tey Putita Ou, et al.
American Journal of Human Genetics
|
June 6, 2003
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome
Dawn H Siegel, Gabrielle H S Ashton, Homero G Penagos, et al.
Page
of 58
Search research articles
Search
Showing results (561-570 of 577) with videos related to
Sort By:
Page
of 58
Human Molecular Genetics
|
August 14, 2003
An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome
W H Irwin McLean, Alan D Irvine, Kevin J Hamill, et al.
Elife
|
January 17, 2015
The contrasting phylodynamics of human influenza B viruses
Dhanasekaran Vijaykrishna, Edward C Holmes, Udayan Joseph, et al.
Nature Genetics
|
April 10, 2007
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
Aileen Sandilands, Ana Terron-Kwiatkowski, Peter R Hull, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 14, 2006
Establishment of multiple sublineages of H5N1 influenza virus in Asia: implications for pandemic control
H Chen, G J D Smith, K S Li, et al.
BMJ Global Health
|
February 6, 2026
Strengthening supply chains for pathogen genomic surveillance in Asia
Anne-Claire Stona, Yoong Khean Khoo, La Moe, et al.
Nature Genetics
|
October 16, 2012
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma
Elizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.
Virus Evolution
|
January 19, 2023
Genomic epidemiology of SARS-CoV-2 in Cambodia, January 2020 to February 2021
Yvonne C F Su, Jordan Z J Ma, Tey Putita Ou, et al.
Lancet (London, England)
|
August 22, 2020
Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
Barnaby E Young, Siew-Wai Fong, Yi-Hao Chan, et al.
Communications Medicine
|
November 28, 2024
Spatiotemporal evolution and transmission dynamics of Alpha and Delta SARS-CoV-2 variants contributing to sequential outbreaks in Cambodia during 2021
Yvonne C F Su, Michael A Zeller, Tey Putita Ou, et al.
American Journal of Human Genetics
|
June 6, 2003
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome
Dawn H Siegel, Gabrielle H S Ashton, Homero G Penagos, et al.
Page
of 58