Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Mathew

Showing results (371-380 of 564) with videos related to

Pageof 57
Sort By:
Inflammatory Bowel Diseases|June 29, 2006
Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's diseaseDavid A van Heel, Karen A Hunt, Kathy King, et al.
Nucleic Acids Research|September 26, 1988
BclI RFLP for the human vimentin geneE M Marcus, B A Smith, H Telenius, et al.
BMC Genomics|December 22, 2007
Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expressionPhilip Rosenstiel, Klaus Huse, Andre Franke, et al.
Tissue Antigens|September 28, 2005
A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British populationN J Prescott, S A Fisher, C Onnie, et al.
Rheumatology (Oxford, England)|February 22, 2003
Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15S Steer, S A Fisher, M Fife, et al.
Journal of Medical Genetics|January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXEA J Barnicoat, Q Wang, J Turk, et al.
Klinische Wochenschrift|September 15, 1989
Early diagnosis of multiple endocrine neoplasia type IIaH P Neumann, O A Müller, B A Ponder, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1990
[Diagnosis of multiple endocrine neoplasms type IIa using DNA analysis]H P Neumann, O A Müller, B A Ponder, et al.
JCO Global Oncology|April 15, 2026
Lifestyle and Environmental Risk Factors for Esophageal Squamous Cell Carcinoma: Evidence From the Johannesburg Cancer StudyWenlong Carl Chen, Debbie Bradshaw, Thendo Ramaliba, et al.
Human Mutation|February 6, 1998
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstreamJ R Lo Ten Foe, F A Kruyt, M B Zweekhorst, et al.
Pageof 57

Showing results (371-380 of 564) with videos related to

Sort By:
Pageof 57
Inflammatory Bowel Diseases|June 29, 2006
Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's diseaseDavid A van Heel, Karen A Hunt, Kathy King, et al.
Nucleic Acids Research|September 26, 1988
BclI RFLP for the human vimentin geneE M Marcus, B A Smith, H Telenius, et al.
BMC Genomics|December 22, 2007
Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expressionPhilip Rosenstiel, Klaus Huse, Andre Franke, et al.
Tissue Antigens|September 28, 2005
A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British populationN J Prescott, S A Fisher, C Onnie, et al.
Rheumatology (Oxford, England)|February 22, 2003
Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15S Steer, S A Fisher, M Fife, et al.
Journal of Medical Genetics|January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXEA J Barnicoat, Q Wang, J Turk, et al.
Klinische Wochenschrift|September 15, 1989
Early diagnosis of multiple endocrine neoplasia type IIaH P Neumann, O A Müller, B A Ponder, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1990
[Diagnosis of multiple endocrine neoplasms type IIa using DNA analysis]H P Neumann, O A Müller, B A Ponder, et al.
JCO Global Oncology|April 15, 2026
Lifestyle and Environmental Risk Factors for Esophageal Squamous Cell Carcinoma: Evidence From the Johannesburg Cancer StudyWenlong Carl Chen, Debbie Bradshaw, Thendo Ramaliba, et al.
Human Mutation|February 6, 1998
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstreamJ R Lo Ten Foe, F A Kruyt, M B Zweekhorst, et al.
Pageof 57