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

Martijn H Breuning

Showing results (71-80 of 112) with videos related to

Pageof 12
Sort By:
The Journal of Biological Chemistry|April 17, 2004
Aberrant polycystin-1 expression results in modification of activator protein-1 activity, whereas Wnt signaling remains unaffectedNgoc Hang Le, Paola van der Bent, Gerwin Huls, et al.
Stroke|February 3, 2007
Lacunar infarcts are the main correlate with cognitive dysfunction in CADASILMichael K Liem, Jeroen van der Grond, Joost Haan, et al.
Journal of Clinical Immunology|March 3, 2016
Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patientsInge C de Vor, Pomme M van der Meulen, Vincent Bekker, et al.
British Journal of Haematology|July 26, 2002
Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB-MYH11 gene fusionBert A van der Reijden, Annet Simons, Erna Luiten, et al.
European Journal of Medical Genetics|June 15, 2010
Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypesAntoinet C J Gijsbers, Cathy A J Bosch, Johannes G Dauwerse, et al.
Human Molecular Genetics|October 22, 2004
Lowering of Pkd1 expression is sufficient to cause polycystic kidney diseaseIrma S Lantinga-van Leeuwen, Johannes G Dauwerse, Hans J Baelde, et al.
American Journal of Human Genetics|February 12, 2005
Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause diseaseJeroen H Roelfsema, Stefan J White, Yavuz Ariyürek, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North AmericaRowida Almomani, Yu Sun, Emmelien Aten, et al.
European Journal of Endocrinology|February 9, 2007
Growth hormone secretion and immunological function of a male patient with a homozygous STAT5b mutationMarie J E Walenkamp, Solrun Vidarsdottir, Alberto M Pereira, et al.
American Journal of Human Genetics|July 6, 2010
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA geneYu Sun, Rowida Almomani, Emmelien Aten, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
The Journal of Biological Chemistry|April 17, 2004
Aberrant polycystin-1 expression results in modification of activator protein-1 activity, whereas Wnt signaling remains unaffectedNgoc Hang Le, Paola van der Bent, Gerwin Huls, et al.
Stroke|February 3, 2007
Lacunar infarcts are the main correlate with cognitive dysfunction in CADASILMichael K Liem, Jeroen van der Grond, Joost Haan, et al.
Journal of Clinical Immunology|March 3, 2016
Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patientsInge C de Vor, Pomme M van der Meulen, Vincent Bekker, et al.
British Journal of Haematology|July 26, 2002
Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB-MYH11 gene fusionBert A van der Reijden, Annet Simons, Erna Luiten, et al.
European Journal of Medical Genetics|June 15, 2010
Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypesAntoinet C J Gijsbers, Cathy A J Bosch, Johannes G Dauwerse, et al.
Human Molecular Genetics|October 22, 2004
Lowering of Pkd1 expression is sufficient to cause polycystic kidney diseaseIrma S Lantinga-van Leeuwen, Johannes G Dauwerse, Hans J Baelde, et al.
American Journal of Human Genetics|February 12, 2005
Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause diseaseJeroen H Roelfsema, Stefan J White, Yavuz Ariyürek, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North AmericaRowida Almomani, Yu Sun, Emmelien Aten, et al.
European Journal of Endocrinology|February 9, 2007
Growth hormone secretion and immunological function of a male patient with a homozygous STAT5b mutationMarie J E Walenkamp, Solrun Vidarsdottir, Alberto M Pereira, et al.
American Journal of Human Genetics|July 6, 2010
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA geneYu Sun, Rowida Almomani, Emmelien Aten, et al.
Pageof 12