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Liver International : Official Journal of the International Association for the Study of the Liver
|
February 16, 2021
Exome sequencing in patient-parent trios suggests new candidate genes for early-onset primary sclerosing cholangitis
Sjoukje-Marije Haisma, Rinse K Weersma, Maria E Joosse, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
May 21, 2016
Androgen-sensitive hypertension associated with soluble guanylate cyclase-α1 deficiency is mediated by 20-HETE
Ana C Dordea, Sara Vandenwijngaert, Victor Garcia, et al.
Nature Genetics
|
August 4, 2014
A framework for the interpretation of de novo mutation in human disease
Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.
Plos Genetics
|
September 27, 2013
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis
Mélissa Beaudoin, Philippe Goyette, Gabrielle Boucher, et al.
Cell
|
July 27, 2019
Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis
Christopher S Smillie, Moshe Biton, Jose Ordovas-Montanes, et al.
Inflammatory Bowel Diseases
|
August 21, 2018
Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease
Lee A Denson, Ingrid Jurickova, Rebekah Karns, et al.
Plos Genetics
|
April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls
Li Liu, Aniko Sabo, Benjamin M Neale, et al.
Gastroenterology
|
February 19, 2018
Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease
Lee A Denson, Ingrid Jurickova, Rebekah Karns, et al.
Nature Genetics
|
October 11, 2011
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
Manuel A Rivas, Mélissa Beaudoin, Agnes Gardet, et al.
Cell
|
January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
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of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
Liver International : Official Journal of the International Association for the Study of the Liver
|
February 16, 2021
Exome sequencing in patient-parent trios suggests new candidate genes for early-onset primary sclerosing cholangitis
Sjoukje-Marije Haisma, Rinse K Weersma, Maria E Joosse, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
May 21, 2016
Androgen-sensitive hypertension associated with soluble guanylate cyclase-α1 deficiency is mediated by 20-HETE
Ana C Dordea, Sara Vandenwijngaert, Victor Garcia, et al.
Nature Genetics
|
August 4, 2014
A framework for the interpretation of de novo mutation in human disease
Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.
Plos Genetics
|
September 27, 2013
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis
Mélissa Beaudoin, Philippe Goyette, Gabrielle Boucher, et al.
Cell
|
July 27, 2019
Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis
Christopher S Smillie, Moshe Biton, Jose Ordovas-Montanes, et al.
Inflammatory Bowel Diseases
|
August 21, 2018
Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease
Lee A Denson, Ingrid Jurickova, Rebekah Karns, et al.
Plos Genetics
|
April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls
Li Liu, Aniko Sabo, Benjamin M Neale, et al.
Gastroenterology
|
February 19, 2018
Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease
Lee A Denson, Ingrid Jurickova, Rebekah Karns, et al.
Nature Genetics
|
October 11, 2011
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
Manuel A Rivas, Mélissa Beaudoin, Agnes Gardet, et al.
Cell
|
January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Page
of 6