Overview

complementation group


'complementation group' can also refer to...

complementation group

complementation group

Homotopy groups of complements and nonisolated singularities

Cohomology of Hyperplane Complements with Group Ring Coefficients

Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M

Genetic and Molecular Definition of Complementation Group D in MHC Class II Deficiency

Mutations in PEX10 Is the Cause of Zellweger Peroxisome Deficiency Syndrome of Complementation Group B

Damage-dependent regulation of MUS81-EME1 by Fanconi anemia complementation group A protein

Human Complement Bactericidal Responses to a Group A Meningococcal Conjugate Vaccine in Africans and Comparison to Responses Measured by 2 Other Group A Immunoassays

Prognostic Significance of X-ray Cross-complementing Group 1 T-77C Polymorphism in Resected Non-small Cell Lung Cancer

Human Immune Response to Streptococcal Inhibitor of Complement, a Serotype M1 Group A Streptococcus Extracellular Protein Involved in Epidemics

Distribution of Streptococcal Inhibitor of Complement Variants in Pharyngitis and Invasive Isolates in an Epidemic of Serotype M1 Group A Streptococcus Infection

Fanconi anemia, complementation group A, cells are defective in ability to produce incisions at sites of psoralen interstrand cross-links

Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders

Molecular Basis for Methionine Synthase Reductase Deficiency in Patients Belonging to the cblE Complementation Group of Disorders in Folate/Cobalamin Metabolism

Nonsense and Temperature-Sensitive Mutations in PEX13 are the Cause of Complementation Group H of Peroxisome Biogenesis Disorders

Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria

Rodent UV-Sensitive Mutant Cell Lines in Complementation Groups 6–10 Have Normal General Excision Repair Activity

Isolation of camptothecin-sensitive Chinese hamster cell mutants: phenotypic heterogeneity within the ataxia telangiectasia-like XRCC8 (irs2) complementation group

 

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Mutants lying within the same cistron; more properly called a noncomplementation group.

Subjects: Genetics and Genomics.


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