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

W Wuyts

Showing results (31-40 of 51) with videos related to

Pageof 6
Sort By:
European Journal of Human Genetics : EJHG|August 10, 1999
Molecular and clinical examination of an Italian DEFECT11 familyW Wuyts, G Di Gennaro, F Bianco, et al.
British Journal of Cancer|October 21, 2010
KRAS mutation detection and prognostic potential in sporadic colorectal cancer using high-resolution melting analysisV Deschoolmeester, C Boeckx, M Baay, et al.
Genomics|February 28, 1998
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene familyW Van Hul, W Wuyts, J Hendrickx, et al.
Cytogenetics and Cell Genetics|November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 geneW Wuyts, N Spieker, N Van Roy, et al.
American Journal of Respiratory and Critical Care Medicine|April 3, 2001
Mechanisms of interleukin 1beta-induced human airway smooth muscle hyporesponsiveness to histamine. Involvement of p38 MAPK NF-kappaBJ L Pype, H Xu, M Schuermans, et al.
Bone|February 13, 2001
Evaluation of the role of RANK and OPG genes in Paget's disease of boneW Wuyts, L Van Wesenbeeck, A Morales-Piga, et al.
American Journal of Human Genetics|August 12, 1999
EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomasJ V Bovée, A M Cleton-Jansen, W Wuyts, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.
American Journal of Human Genetics|September 14, 2001
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35L J Hocking, C A Herbert, R K Nicholls, et al.
American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
European Journal of Human Genetics : EJHG|August 10, 1999
Molecular and clinical examination of an Italian DEFECT11 familyW Wuyts, G Di Gennaro, F Bianco, et al.
British Journal of Cancer|October 21, 2010
KRAS mutation detection and prognostic potential in sporadic colorectal cancer using high-resolution melting analysisV Deschoolmeester, C Boeckx, M Baay, et al.
Genomics|February 28, 1998
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene familyW Van Hul, W Wuyts, J Hendrickx, et al.
Cytogenetics and Cell Genetics|November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 geneW Wuyts, N Spieker, N Van Roy, et al.
American Journal of Respiratory and Critical Care Medicine|April 3, 2001
Mechanisms of interleukin 1beta-induced human airway smooth muscle hyporesponsiveness to histamine. Involvement of p38 MAPK NF-kappaBJ L Pype, H Xu, M Schuermans, et al.
Bone|February 13, 2001
Evaluation of the role of RANK and OPG genes in Paget's disease of boneW Wuyts, L Van Wesenbeeck, A Morales-Piga, et al.
American Journal of Human Genetics|August 12, 1999
EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomasJ V Bovée, A M Cleton-Jansen, W Wuyts, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.
American Journal of Human Genetics|September 14, 2001
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35L J Hocking, C A Herbert, R K Nicholls, et al.
American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.
Pageof 6