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

M de Weers

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Human Molecular Genetics|November 1, 1992
Three dinucleotide repeat polymorphisms at the DXS178 locusM de Weers, R G Mensink, M Kenter, et al.
Clinical Genetics|July 1, 1995
Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia MM E Kraakman, M de Weers, T Español, et al.
Clinical Immunology and Immunopathology|November 1, 1991
X-linked agammaglobulinemiaE Timmers, M de Weers, F W Alt, et al.
Human Molecular Genetics|January 1, 1994
Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid miceM de Weers, R G Mensink, M E Kraakman, et al.
Immunodeficiency|January 1, 1993
X chromosome inactivation patterns in leucocyte populations of female carriers of Wiskott-Aldrich syndrome with an atypical presentationM de Weers, R G Mensink, M E Kraakman, et al.
Human Immunology|April 1, 1993
Mhc-DRB and -DQA1 nucleotide sequences of three lowland gorillas. Implications for the evolution of primate Mhc class II haplotypesM Kenter, N Otting, M de Weers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 5, 1990
[Genetic carrier detection for the Wiskott-Aldrich syndrome using restriction fragment length polymorphism analysis]M de Weers, G J Kolvenbag, I F Versteegde, et al.
The Journal of Biological Chemistry|September 30, 1994
B-cell antigen receptor stimulation activates the human Bruton's tyrosine kinase, which is deficient in X-linked agammaglobulinemiaM de Weers, G S Brouns, S Hinshelwood, et al.
European Journal of Immunology|December 1, 1993
The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stagesM de Weers, M C Verschuren, M E Kraakman, et al.
Clinical and Experimental Immunology|May 1, 1991
Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locusR W Hendriks, M De Weers, R G Mensink, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|November 1, 1992
Three dinucleotide repeat polymorphisms at the DXS178 locusM de Weers, R G Mensink, M Kenter, et al.
Clinical Genetics|July 1, 1995
Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia MM E Kraakman, M de Weers, T Español, et al.
Clinical Immunology and Immunopathology|November 1, 1991
X-linked agammaglobulinemiaE Timmers, M de Weers, F W Alt, et al.
Human Molecular Genetics|January 1, 1994
Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid miceM de Weers, R G Mensink, M E Kraakman, et al.
Immunodeficiency|January 1, 1993
X chromosome inactivation patterns in leucocyte populations of female carriers of Wiskott-Aldrich syndrome with an atypical presentationM de Weers, R G Mensink, M E Kraakman, et al.
Human Immunology|April 1, 1993
Mhc-DRB and -DQA1 nucleotide sequences of three lowland gorillas. Implications for the evolution of primate Mhc class II haplotypesM Kenter, N Otting, M de Weers, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 5, 1990
[Genetic carrier detection for the Wiskott-Aldrich syndrome using restriction fragment length polymorphism analysis]M de Weers, G J Kolvenbag, I F Versteegde, et al.
The Journal of Biological Chemistry|September 30, 1994
B-cell antigen receptor stimulation activates the human Bruton's tyrosine kinase, which is deficient in X-linked agammaglobulinemiaM de Weers, G S Brouns, S Hinshelwood, et al.
European Journal of Immunology|December 1, 1993
The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stagesM de Weers, M C Verschuren, M E Kraakman, et al.
Clinical and Experimental Immunology|May 1, 1991
Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locusR W Hendriks, M De Weers, R G Mensink, et al.
Pageof 2