Literature DB >> 1682232

Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.

G Van Camp1, H Backhovens, M Cruts, A Wehnert, W Van Hul, P Stinissen, C Van Broeckhoven.   

Abstract

Linkage studies in families with presenile onset of Alzheimer's disease (AD) indicated the presence of a predisposing gene on the proximal long arm of chromosome 21. We mapped four new loci in the candidate AD region using somatic cell hybrids. For three of the four loci, several restriction fragment length polymorphisms were found; for one locus, a multiallelic (CA)n dinucleotide polymorphism was detected. Preliminary genetic mapping of the new polymorphic loci relative to the AD-linked loci was obtained in a reference pedigree. In addition, we used the (CA)n dinucleotide polymorphism to reconstruct the non-disjunction event in a Down syndrome (DS) patient whose mother died of familial AD.

Entities:  

Mesh:

Year:  1991        PMID: 1682232     DOI: 10.1007/bf00201718

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


  25 in total

1.  Predisposing locus for Alzheimer's disease on chromosome 21.

Authors:  A M Goate; A R Haynes; M J Owen; M Farrall; L A James; L Y Lai; M J Mullan; P Roques; M N Rossor; R Williamson
Journal:  Lancet       Date:  1989-02-18       Impact factor: 79.321

2.  An improved technique for the efficient construction of gene libraries by partial filling-in of cohesive ends.

Authors:  E R Zabarovsky; R L Allikmets
Journal:  Gene       Date:  1986       Impact factor: 3.688

3.  Use of restriction fragment length polymorphic probes in the analysis of Down's syndrome trisomy.

Authors:  A M Millington-Ward; P L Pearson
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

Authors:  P H St George-Hyslop; J L Haines; L A Farrer; R Polinsky; C Van Broeckhoven; A Goate; D R McLachlan; H Orr; A C Bruni; S Sorbi; I Rainero; J F Foncin; D Pollen; J M Cantu; R Tupler; N Voskresenskaya; R Mayeux; J Growden; V A Fried; R H Myers; L Nee; H Backhovens; J J Martin; M Rossor; M J Owen; M Mullan; M E Percy; H Karlinsky; S Rich; L Heston; M Montesi; M Mortilla; N Nacmias; J F Gusella; J A Hardy
Journal:  Nature       Date:  1990-09-13       Impact factor: 49.962

5.  Genomic sequencing.

Authors:  G M Church; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

6.  Mapping the human amylase gene cluster on the proximal short arm of chromosome 1 using a highly informative (CA)n repeat.

Authors:  N C Dracopoli; M H Meisler
Journal:  Genomics       Date:  1990-05       Impact factor: 5.736

Review 7.  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

8.  Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease.

Authors:  G D Schellenberg; T D Bird; E M Wijsman; D K Moore; M Boehnke; E M Bryant; T H Lampe; D Nochlin; S M Sumi; S S Deeb
Journal:  Science       Date:  1988-09-16       Impact factor: 47.728

9.  Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy.

Authors:  P Raeymaekers; P De Jonghe; L Swerts; L Muylle; J Gheuens; J J Martin; C Van Broeckhoven; A Vandenberghe
Journal:  J Neurol Sci       Date:  1988-12       Impact factor: 3.181

10.  Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids.

Authors:  G Van Camp; W Van Hul; H Backhovens; P Stinissen; A Wehnert; D Patterson; A Vandenberghe; C Van Broeckhoven
Journal:  Somat Cell Mol Genet       Date:  1990-05
View more
  5 in total

1.  Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

Authors:  M B Peterson; M Frantzen; S E Antonarakis; A C Warren; C Van Broeckhoven; A Chakravarti; T K Cox; C Lund; B Olsen; H Poulsen
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

2.  DNA polymorphism analysis in families with recurrence of free trisomy 21.

Authors:  C G Pangalos; C C Talbot; J G Lewis; P A Adelsberger; M B Petersen; J L Serre; M O Rethoré; M C de Blois; P Parent; A A Schinzel
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

3.  Dinucleotide repeat polymorphism at the D21S145 locus.

Authors:  M Cruts; H Backhovens; C Van Broeckhoven
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

4.  Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.

Authors:  O Bartsch; U König; M B Petersen; H Poulsen; M Mikkelsen; F Palau; F Prieto; E Schwinger
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

5.  Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization.

Authors:  C Voorter; S Joos; P P Bringuier; M Vallinga; P Poddighe; J Schalken; S du Manoir; F Ramaekers; P Lichter; A Hopman
Journal:  Am J Pathol       Date:  1995-06       Impact factor: 4.307

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.