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American Journal of Medical Genetics. Part A
|
July 22, 2014
Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome
Christopher M Watson, Laura A Crinnion, Antigoni Tzika, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 29, 2020
Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertions
Christopher M Watson, Laura A Crinnion, Helen Lindsay, et al.
Science Translational Medicine
|
October 13, 2017
An analysis of IL-36 signature genes and individuals with <i>IL1RL2</i> knockout mutations validates IL-36 as a psoriasis therapeutic target
Satveer K Mahil, Marika Catapano, Paola Di Meglio, et al.
Annals of the Rheumatic Diseases
|
February 5, 2021
Targeting human plasmacytoid dendritic cells through BDCA2 prevents skin inflammation and fibrosis in a novel xenotransplant mouse model of scleroderma
Rebecca L Ross, Clarissa Corinaldesi, Gemma Migneco, et al.
Scientific Reports
|
July 22, 2017
Paracrine cyclooxygenase-2 activity by macrophages drives colorectal adenoma progression in the Apc <sup>Min/+</sup> mouse model of intestinal tumorigenesis
Mark A Hull, Richard J Cuthbert, C W Stanley Ko, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 19, 2016
Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1
Leman Damla Kotan, Charlton Cooper, Şükran Darcan, et al.
Molecular Phylogenetics and Evolution
|
January 29, 2025
Genomic insights into the biogeography and evolution of Galápagos iguanas
Cecilia Paradiso, Paolo Gratton, Emiliano Trucchi, et al.
Human Mutation
|
December 6, 2013
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface
Christopher M Watson, Laura A Crinnion, Joanne E Morgan, et al.
Plos One
|
August 19, 2014
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing
Christopher M Watson, Mohammed El-Asrag, David A Parry, et al.
Nature Genetics
|
May 27, 2008
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy
Sandeep Uppal, Christine P Diggle, Ian M Carr, et al.
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Search research articles
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Showing results (61-70 of 96) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics. Part A
|
July 22, 2014
Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome
Christopher M Watson, Laura A Crinnion, Antigoni Tzika, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 29, 2020
Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertions
Christopher M Watson, Laura A Crinnion, Helen Lindsay, et al.
Science Translational Medicine
|
October 13, 2017
An analysis of IL-36 signature genes and individuals with <i>IL1RL2</i> knockout mutations validates IL-36 as a psoriasis therapeutic target
Satveer K Mahil, Marika Catapano, Paola Di Meglio, et al.
Annals of the Rheumatic Diseases
|
February 5, 2021
Targeting human plasmacytoid dendritic cells through BDCA2 prevents skin inflammation and fibrosis in a novel xenotransplant mouse model of scleroderma
Rebecca L Ross, Clarissa Corinaldesi, Gemma Migneco, et al.
Scientific Reports
|
July 22, 2017
Paracrine cyclooxygenase-2 activity by macrophages drives colorectal adenoma progression in the Apc <sup>Min/+</sup> mouse model of intestinal tumorigenesis
Mark A Hull, Richard J Cuthbert, C W Stanley Ko, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 19, 2016
Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1
Leman Damla Kotan, Charlton Cooper, Şükran Darcan, et al.
Molecular Phylogenetics and Evolution
|
January 29, 2025
Genomic insights into the biogeography and evolution of Galápagos iguanas
Cecilia Paradiso, Paolo Gratton, Emiliano Trucchi, et al.
Human Mutation
|
December 6, 2013
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface
Christopher M Watson, Laura A Crinnion, Joanne E Morgan, et al.
Plos One
|
August 19, 2014
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing
Christopher M Watson, Mohammed El-Asrag, David A Parry, et al.
Nature Genetics
|
May 27, 2008
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy
Sandeep Uppal, Christine P Diggle, Ian M Carr, et al.
Page
of 10