Literature DB >> 1968036

Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region.

J S Wu1, K K Kidd.   

Abstract

Extensive sequence polymorphisms exist in the chromosome 10 alpha satellite DNA (the D10Z1 locus). Polymorphic morphs revealed by the enzymes PstI, EcoRV, and HincII, can be unambiguously scored and make this centromeric region an excellent genetic marker for the study of multiple endocrine neoplasia, type 2A (MEN2A), as well as for chromosome 10 linkage studies in general. Strong positive lod scores and linkage distance relationships between D10Z1 and DNA markers from the chromosome 10 pericentromeric region, especially FNRB and RBP3, known to be on either side of the centromere, provide independent support for mapping of all these loci.

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Year:  1990        PMID： 1968036     DOI： 10.1007/bf00200575

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


  12 in total

1.  A computer program for linkage analysis of general human pedigrees.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

2.  A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes.

Authors:  A R Mitchell; J R Gosden; D A Miller
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

3.  Chromosome-specific subfamilies within human alphoid repetitive DNA.

Authors:  A L Jørgensen; C J Bostock; A L Bak
Journal:  J Mol Biol       Date:  1986-01-20       Impact factor: 5.469

4.  Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.

Authors:  H F Willard; J S Waye; M H Skolnick; C E Schwartz; V E Powers; S B England
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

5.  The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.

Authors:  J S Wu; L A Giuffra; P J Goodfellow; S Myers; N L Carson; L Anderson; L S Hoyle; N E Simpson; K K Kidd
Journal:  Hum Genet       Date:  1989-11       Impact factor: 4.132

6.  Close linkage of MT2P1 with GC on chromosome 4.

Authors:  A J Pakstis; J R Kidd; C Castiglione; R S Sparkes; K K Kidd
Journal:  Cytogenet Cell Genet       Date:  1986

7.  Chromosome-specific alpha satellite DNA: isolation and mapping of a polymorphic alphoid repeat from human chromosome 10.

Authors:  P Devilee; T Kievits; J S Waye; P L Pearson; H F Willard
Journal:  Genomics       Date:  1988-07       Impact factor: 5.736

8.  Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11.

Authors:  J S Waye; G M Greig; H F Willard
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

9.  Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation.

Authors:  E W Jabs; S F Wolf; B R Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

10.  Assignment of the gene encoding the beta-subunit of the human fibronectin receptor (beta-FNR) to chromosome 10p11.2.

Authors:  P J Goodfellow; H A Nevanlinna; P Gorman; D Sheer; G Lam; P N Goodfellow
Journal:  Ann Hum Genet       Date:  1989-01       Impact factor: 1.670
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  8 in total

1.  Characterisation of a boundary between satellite III and alphoid sequences on human chromosome 10.

Authors:  M S Jackson; S E Mole; B A Ponder
Journal:  Nucleic Acids Res       Date:  1992-09-25       Impact factor: 16.971

2.  Consensus higher order repeats and frequency of string distributions in human genome.

Authors:  Vladimir Paar; Ivan Basar; Marija Rosandić; Matko Gluncić
Journal:  Curr Genomics       Date:  2007-04       Impact factor: 2.236

3.  The gene for MEN 2A is tightly linked to the centromere of chromosome 10.

Authors:  S A Narod; H Sobol; I Schuffenecker; M F Lavoué; G M Lenoir
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

4.  Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.

Authors:  S A Narod; M F Lavoué; K Morgan; C Calmettes; H Sobol; P J Goodfellow; G M Lenoir
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

5.  A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.

Authors:  J B Lichter; J Wu; A R Brooks-Wilson; M Difillipantonio; S Brewster; D C Ward; P J Goodfellow; K K Kidd
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132

Review 6.  An historical perspective on "The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus".

Authors:  Kenneth K Kidd; Andrew J Pakstis; Libing Yun
Journal:  Hum Genet       Date:  2013-10-27       Impact factor: 4.132

7.  The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.

Authors:  N L Carson; J S Wu; C E Jackson; K K Kidd; N E Simpson
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

8.  CENP-B box and pJalpha sequence distribution in human alpha satellite higher-order repeats (HOR).

Authors:  Marija Rosandić; Vladimir Paar; Ivan Basar; Matko Gluncić; Nenad Pavin; Ivan Pilas
Journal:  Chromosome Res       Date:  2006-11-22       Impact factor: 4.620
  8 in total

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