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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 syndromeW H Irwin McLean, Alan D Irvine, Kevin J Hamill, et al.

Elife|January 17, 2015

The contrasting phylodynamics of human influenza B virusesDhanasekaran 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 eczemaAileen 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 controlH Chen, G J D Smith, K S Li, et al.

BMJ Global Health|February 6, 2026

Strengthening supply chains for pathogen genomic surveillance in AsiaAnne-Claire Stona, Yoong Khean Khoo, La Moe, et al.

Nature Genetics|October 16, 2012

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratodermaElizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.

Virus Evolution|January 19, 2023

Genomic epidemiology of SARS-CoV-2 in Cambodia, January 2020 to February 2021Yvonne 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 studyBarnaby 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 2021Yvonne 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 syndromeDawn H Siegel, Gabrielle H S Ashton, Homero G Penagos, et al.

Pageof 58

Showing results (561-570 of 577) with videos related to

Sort By:

Pageof 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 syndromeW H Irwin McLean, Alan D Irvine, Kevin J Hamill, et al.

Elife|January 17, 2015

The contrasting phylodynamics of human influenza B virusesDhanasekaran 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 eczemaAileen 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 controlH Chen, G J D Smith, K S Li, et al.

BMJ Global Health|February 6, 2026

Strengthening supply chains for pathogen genomic surveillance in AsiaAnne-Claire Stona, Yoong Khean Khoo, La Moe, et al.

Nature Genetics|October 16, 2012

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratodermaElizabeth Pohler, Ons Mamai, Jennifer Hirst, et al.

Virus Evolution|January 19, 2023

Genomic epidemiology of SARS-CoV-2 in Cambodia, January 2020 to February 2021Yvonne 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 studyBarnaby 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 2021Yvonne 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 syndromeDawn H Siegel, Gabrielle H S Ashton, Homero G Penagos, et al.

Pageof 58