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Jan Osinga

Showing results (11-20 of 19) with videos related to

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Human Molecular Genetics|July 13, 2010
KBP interacts with SCG10, linking Goldberg-Shprintzen syndrome to microtubule dynamics and neuronal differentiationMaria M Alves, Grzegorz Burzynski, Jean-Marie Delalande, et al.
Cancer Research|March 9, 2005
RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factorIvan Plaza Menacho, Roelof Koster, Almer M van der Sloot, et al.
Human Genetics|January 13, 2006
MUTYH and the mismatch repair system: partners in crime?Renée C Niessen, Rolf H Sijmons, J Ou, et al.
Gene|October 29, 2013
Relation between genotype and left-ventricular dilatation in patients with Marfan syndromeJan J J Aalberts, J Peter van Tintelen, Lilian J Meijboom, et al.
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndromeMark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Human Mutation|September 19, 2014
New target genes in endometrial tumors show a role for the estrogen-receptor pathway in microsatellite-unstable cancersAna M Ferreira, Iina Tuominen, Sónia Sousa, et al.
Journal of the American College of Cardiology|June 30, 2007
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C geneJ Peter van Tintelen, Rene A Tio, Wilhelmina S Kerstjens-Frederikse, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Molecular Genetics|July 13, 2010
KBP interacts with SCG10, linking Goldberg-Shprintzen syndrome to microtubule dynamics and neuronal differentiationMaria M Alves, Grzegorz Burzynski, Jean-Marie Delalande, et al.
Cancer Research|March 9, 2005
RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factorIvan Plaza Menacho, Roelof Koster, Almer M van der Sloot, et al.
Human Genetics|January 13, 2006
MUTYH and the mismatch repair system: partners in crime?Renée C Niessen, Rolf H Sijmons, J Ou, et al.
Gene|October 29, 2013
Relation between genotype and left-ventricular dilatation in patients with Marfan syndromeJan J J Aalberts, J Peter van Tintelen, Lilian J Meijboom, et al.
American Journal of Human Genetics|May 11, 2005
Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systemsAlice S Brooks, Aida M Bertoli-Avella, Grzegorz M Burzynski, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndromeMark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Human Mutation|September 19, 2014
New target genes in endometrial tumors show a role for the estrogen-receptor pathway in microsatellite-unstable cancersAna M Ferreira, Iina Tuominen, Sónia Sousa, et al.
Journal of the American College of Cardiology|June 30, 2007
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C geneJ Peter van Tintelen, Rene A Tio, Wilhelmina S Kerstjens-Frederikse, et al.
Pageof 2