Literature DB >> 1394787

Nomenclature for human complement component C2. WHO-IUIS Nomenclature Sub-Committee.

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Abstract

This note describes the designations for variants of the human complement component C2, which were approved by the Nomenclature Committee of the International Union of Immunological Societies (IUIS).

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Year:  1992        PMID： 1394787      PMCID： PMC2393382     

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN： 0042-9686            Impact factor:   9.408


  5 in total

1.  C2 reference typing report.

Authors:  I Jahn; B Uring-Lambert; D Arnold; S Clemenceau; G Hauptmann
Journal:  Complement Inflamm       Date:  1990

2.  International system for human gene nomenclature (1979) ISGN (1979).

Authors:  T B Shows; C A Alper; D Bootsma; M Dorf; T Douglas; T Huisman; S Kit; H P Klinger; C Kozak; P A Lalley; D Lindsley; P J McAlpine; J K McDougall; P Meera Khan; M Meisler; N E Morton; J M Opitz; C W Partridge; R Payne; T H Roderick; P Rubinstein; F H Ruddle; M Shaw; J W Spranger; K Weiss
Journal:  Cytogenet Cell Genet       Date:  1979

3.  Mapping of the structural gene for the second component of complement with respect to the human major histocompatibility complex.

Authors:  D Raum; D Glass; C B Carpenter; P H Schur; C A Alper
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

4.  Evidence for a silent or null gene in hereditary C2 deficiency.

Authors:  K M Pariser; D Raum; E M Berkman; C A Alper; V Agnello
Journal:  J Immunol       Date:  1978-12       Impact factor: 5.422

5.  Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.

Authors:  C A Alper
Journal:  J Exp Med       Date:  1976-10-01       Impact factor: 14.307
  5 in total

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