Literature DB >> 6323102

Regional localization of alpha-galactosidase (GLA) to Xpter----q22, hexosaminidase B (HEXB) to 5q13----qter, and arylsulfatase B (ARSB) to 5pter----q13.

M F Fox, D L DuToit, L Warnich, A E Retief.   

Abstract

Two series of somatic cell hybrids were made by fusion of human cells with karyotypes 46,X,t(X;2;15)(q22;p12;p12) and 46,XX,t(5;7)(q13;p15) and rodent cells. Chromosome and isozyme analysis of human chromosomes and gene products in the hybrids localized GLA to Xpter----q22, HEXB to 5q13----qter, in both cases narrowing the regional assignments, and ARSB to 5pter----q13.

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Year:  1984        PMID: 6323102     DOI: 10.1159/000132028

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


  16 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an NcoI polymorphism detected by an alpha-galactosidase cDNA clone.

Authors:  A J Kirkilionis; D C Riddell; M W Spence; R G Fenwick
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

Review 3.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

4.  Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia.

Authors:  B C McGillivray; A S Bassett; S Langlois; T Pantzar; S Wood
Journal:  Am J Med Genet       Date:  1990-01

5.  Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase.

Authors:  T Litjens; E G Baker; K R Beckmann; C P Morris; J J Hopwood; D F Callen
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

6.  Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error.

Authors:  S Schwartz; M F Schwartz; S R Panny; C J Peterson; E Waters; M M Cohen
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

Review 7.  Anderson-Fabry disease.

Authors:  S H Morgan; M A Crawfurd
Journal:  BMJ       Date:  1988-10-08

8.  Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes.

Authors:  S H Morgan; J K Cheshire; T M Wilson; K MacDermot; M A Crawfurd
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

9.  Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).

Authors:  J M Trent; I L Flink; E Morkin; P van Tuinen; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1987-09       Impact factor: 11.025

10.  [Inherited metabolic disorders with cutaneous manifestations].

Authors:  P Poblete-Gutiérrez; T Wiederholt; J Frank
Journal:  Hautarzt       Date:  2004-10       Impact factor: 0.751

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