Literature DB >> 2892777

The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1.

P Raeymaekers1, C Van Broeckhoven, H Backhovens, A Wehnert, L Muylle, P De Jonghe, J Gheuens, A Vandenberghe.   

Abstract

The alpha-spectrin locus (SPTA) on chromosome 1 maps to 1q22-q25 and alpha-spectrin specific probes detect restriction fragment length polymorphisms (RFLPs) with the endonucleases MspI and PvuII. The Duffy blood group (FY) has been mapped to the 1p21-q23 region. We found positive linkage between the alpha-spectrin and the Duffy loci with a maximal Lod score of 3.81 at theta = 0.0 using the computer program MLINK. This indicates that both loci are very closely linked and probably localized to 1q22-q23.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2892777     DOI: 10.1007/bf00291239

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  22 in total

1.  Linkage group I: a statistically significant locus order from family studies.

Authors:  D A Meyers; A D Merritt; P M Conneally; J A Norton; M L Rivas; P L Yu; C G Palmer
Journal:  Cytogenet Cell Genet       Date:  1978

2.  Family data on sixteen chromosome 1 loci.

Authors:  E B Robson; J King
Journal:  Ann Hum Genet       Date:  1984-10       Impact factor: 1.670

3.  A computer program for constructing a maximum-likelihood map from linkage data and its application to human chromosome 1.

Authors:  N Wedd
Journal:  Ann Hum Genet       Date:  1984-10       Impact factor: 1.670

4.  A membrane-filter technique for the detection of complementary DNA.

Authors:  D T Denhardt
Journal:  Biochem Biophys Res Commun       Date:  1966-06-13       Impact factor: 3.575

5.  Sequence comparison of human and murine erythrocyte alpha-spectrin cDNA.

Authors:  P J Curtis; A Palumbo; J Ming; P Fraser; L Cioe; P Meo; S Shane; G Rovera
Journal:  Gene       Date:  1985       Impact factor: 3.688

6.  Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.

Authors:  T D Bird; J Ott; E R Giblett
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

7.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

8.  High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization.

Authors:  B U Zabel; S L Naylor; A Y Sakaguchi; G I Bell; T B Shows
Journal:  Proc Natl Acad Sci U S A       Date:  1983-11       Impact factor: 11.205

Review 9.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

10.  Detection and characterization of a mouse alpha-spectrin cDNA clone by its expression in Escherichia coli.

Authors:  L Cioe; P Curtis
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

View more
  9 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.  Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.

Authors:  R V Lebo; P F Chance; P J Dyck; M T Redila-Flores; E D Lynch; M S Golbus; T D Bird; M C King; L A Anderson; J Hall
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

3.  Multicolor fluorescence in situ hybridization and pulsed field electrophoresis dissect CMT1B gene region.

Authors:  R V Lebo; E D Lynch; J Wiegant; K Moore; M Trounstine; M van der Ploeg
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

Review 4.  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

5.  Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome.

Authors:  G Van Camp; P Stinissen; W Van Hul; H Backhovens; A Wehnert; A Vandenberge; C Van Broeckhoven
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

6.  Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

Authors:  P Raeymaekers; V Timmerman; P De Jonghe; L Swerts; J Gheuens; J J Martin; L Muylle; G De Winter; A Vandenberghe; C Van Broeckhoven
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

7.  Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease.

Authors:  P Raeymaekers; C Van Broeckhoven; H Backhovens; A Wehnert; L Muylle; P De Jonghe; J Gheuens; J J Martin; A Vandenberghe
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

8.  Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.

Authors:  E Nelis; V Timmerman; P De Jonghe; L Muylle; J J Martin; C Van Broeckhoven
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

9.  Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

Authors:  E Bellone; P Mandich; G L Mancardi; A Schenone; A Uccelli; M Abbruzzese; A Sghirlanzoni; D Pareyson; F Ajmar
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.