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Identification of glioma-associated antigen MUC 2-63 as CD44

P Romeijn
R Lenthall
MA Ritter
Research01 Nov 1994
British Journal of Cancer

Volume: 70, P: 799-803
Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

Sander M Houten
Janet Koster
Hans R Waterham
Research20 Apr 2001
European Journal of Human Genetics

Volume: 9, P: 253-259
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

Sander M. Houten
Wietse Kuis
Bwee Tien Poll-The
Research01 Jun 1999
Nature Genetics

Volume: 22, P: 175-177
Helicase Q promotes homology-driven DNA double-strand break repair and prevents tandem duplications

Microhomology-mediated end-joining (MMEJ) is a poorly defined mutagenic DNA break repair pathway. Here the authors show that the helicase HELQ is essential for polymerase theta-independent MMEJ, single-strand annealing and homologous recombination through synthesis dependent strand annealing in C. elegans.

J. A. Kamp
B. B. L. G. Lemmens
M. Tijsterman
ResearchOpen Access08 Dec 2021
Nature Communications

Volume: 12, P: 1-12
Erratum: Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

SanderM Houten
Janet Koster
Hans R Waterham
Amendments and Corrections30 Aug 2001
European Journal of Human Genetics

Volume: 9, P: 651
BRCA1-associated structural variations are a consequence of polymerase theta-mediated end-joining

Cancer mutational signatures have been associated with defects in genome maintenance pathways. Here the authors, by using a worm germline mutagenesis model defective of human orthologue BRCA-1, identify polymerase theta-mediated end-joining (TMEJ) as causing the BRCAness mutational signature.

J. A. Kamp
R. van Schendel
M. Tijsterman
ResearchOpen Access17 Jul 2020
Nature Communications

Volume: 11, P: 1-10

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Identification of glioma-associated antigen MUC 2-63 as CD44

Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

Helicase Q promotes homology-driven DNA double-strand break repair and prevents tandem duplications

Erratum: Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

BRCA1-associated structural variations are a consequence of polymerase theta-mediated end-joining

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Identification of glioma-associated antigen MUC 2-63 as CD44

Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

Helicase Q promotes homology-driven DNA double-strand break repair and prevents tandem duplications

Erratum: Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

BRCA1-associated structural variations are a consequence of polymerase theta-mediated end-joining

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