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Gabriele Mayr

Showing results (11-20 of 29) with videos related to

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European Journal of Gastroenterology & Hepatology|September 11, 2018
Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel diseaseEun Suk Jung, Britt-Sabina Petersen, Gabriele Mayr, et al.
The Journal of Investigative Dermatology|July 25, 2016
Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis RiskJudith Manz, Elke Rodríguez, Abdou ElSharawy, et al.
Plos Biology|September 14, 2007
Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitisCilla Söderhäll, Ingo Marenholz, Tamara Kerscher, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|October 16, 2024
Functional Variation in Human CAZyme Genes in Relation to the Efficacy of a Carbohydrate-Restricted Diet in IBS PatientsAndreea Zamfir-Taranu, Britt-Sabina Löscher, Florencia Carbone, et al.
Gut|February 28, 2014
XIAP variants in male Crohn's diseaseYvonne Zeissig, Britt-Sabina Petersen, Snezana Milutinovic, et al.
Nature Genetics|January 4, 2007
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1Jochen Hampe, Andre Franke, Philip Rosenstiel, et al.
Gut|March 6, 2023
Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patientsAndreea Zamfir-Taranu, Britt-Sabina Löscher, Diab M Husein, et al.
Plos One|August 9, 2007
Systematic association mapping identifies NELL1 as a novel IBD disease geneAndre Franke, Jochen Hampe, Philip Rosenstiel, et al.
Cold Spring Harbor Molecular Case Studies|February 3, 2019
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2Simone Lipinski, Britt-Sabina Petersen, Matthias Barann, et al.
Nature Genetics|October 7, 2008
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibilityAndre Franke, Tobias Balschun, Tom H Karlsen, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
European Journal of Gastroenterology & Hepatology|September 11, 2018
Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel diseaseEun Suk Jung, Britt-Sabina Petersen, Gabriele Mayr, et al.
The Journal of Investigative Dermatology|July 25, 2016
Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis RiskJudith Manz, Elke Rodríguez, Abdou ElSharawy, et al.
Plos Biology|September 14, 2007
Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitisCilla Söderhäll, Ingo Marenholz, Tamara Kerscher, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|October 16, 2024
Functional Variation in Human CAZyme Genes in Relation to the Efficacy of a Carbohydrate-Restricted Diet in IBS PatientsAndreea Zamfir-Taranu, Britt-Sabina Löscher, Florencia Carbone, et al.
Gut|February 28, 2014
XIAP variants in male Crohn's diseaseYvonne Zeissig, Britt-Sabina Petersen, Snezana Milutinovic, et al.
Nature Genetics|January 4, 2007
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1Jochen Hampe, Andre Franke, Philip Rosenstiel, et al.
Gut|March 6, 2023
Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patientsAndreea Zamfir-Taranu, Britt-Sabina Löscher, Diab M Husein, et al.
Plos One|August 9, 2007
Systematic association mapping identifies NELL1 as a novel IBD disease geneAndre Franke, Jochen Hampe, Philip Rosenstiel, et al.
Cold Spring Harbor Molecular Case Studies|February 3, 2019
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2Simone Lipinski, Britt-Sabina Petersen, Matthias Barann, et al.
Nature Genetics|October 7, 2008
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibilityAndre Franke, Tobias Balschun, Tom H Karlsen, et al.
Pageof 3