Literature DB >> 7192199

Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22.

A H Geurts van Kessel, A Westerveld, P G de Groot, P Meera Khan, A Hagemeijer.   

Abstract

The segregation of the chromosome 22 markers ACO2, ARSA, and NAGA was studied in somatic cell hybrid clones. These hybrids were isolated following fusion of Chinese hamster (E36 or a3) cells with leucocytes of donors carrying an (X;22) or (1;22) translocation. The results suggest the assignment of ARSA and NAGA to the region 22q13 leads to 22qter and of ACO2 to the region 22q11 leads to 22q13.

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Year:  1980        PMID： 7192199     DOI： 10.1159/000131527

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  19 in total

1.  The human transmembrane secretory component (poly-Ig receptor): molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization.

Authors:  P Krajci; K H Grzeschik; A H Geurts van Kessel; B Olaisen; P Brandtzaeg
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

2.  BamHI polymorphism at N-acetyl-alpha-galactosaminidase locus (NAGA).

Authors:  T Yamauchi; H Tanaka; M Hiraiwa; Y Uda; T Miyatake; S Tsuji
Journal:  Nucleic Acids Res       Date:  1991-05-11       Impact factor: 16.971

3.  Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome.

Authors:  A M Sharkey; L McLaren; M Carroll; J Fantes; D Green; D Wilson; P J Scambler; H J Evans
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

4.  A BamHI RFLP in the human arylsulfatase A gene.

Authors:  A Polten; V Gieselmann
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

5.  A TaqI RFLP for the human arylsulfatase A gene.

Authors:  R Herzog; K Holzmann; N Blin
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

6.  Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter.

Authors:  J P Dumanski; A H Geurts van Kessel; M Ruttledge; A Wladis; N Sugawa; V P Collins; M Nordenskjöld
Journal:  Hum Genet       Date:  1990-02       Impact factor: 4.132

7.  Myoclonic epilepsy of Lafora and arylsulphatase A deficiency in the same patient.

Authors:  B Bertagnolio; F Girotti; D Pelucchetti; M Pandolfo
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

8.  The human myoglobin gene: a third dispersed globin locus in the human genome.

Authors:  A J Jeffreys; V Wilson; A Blanchetot; P Weller; A Geurts van Kessel; N Spurr; E Solomon; P Goodfellow
Journal:  Nucleic Acids Res       Date:  1984-04-11       Impact factor: 16.971

9.  Chromosomal localization of three human genes coding for A15, L6, and S5.7 (TAPA1): all members of the transmembrane 4 superfamily of proteins.

Authors:  K I Virtaneva; N Emi; J S Marken; A Aruffo; C Jones; N K Spurr; J P Schröder
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

Review 10.  Human chromosome 22.

Authors:  J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318
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