Literature DB >> 2119504

Genetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17.

M K Yagle1, G Parruti, W Xu, B A Ponder, E Solomon.   

Abstract

The von Recklinghausen neurofibromatosis 1 (NF1) locus has been previously assigned to the proximal long arm of chromosome 17, and two NF1 patients have been identified who have constitutional balanced translocations involving 17q11.2. We have constructed a cosmid library from a chromosome-mediated gene transfectant, KLT8, that contains approximately 10% of chromosome 17, including 17q11.2. Cosmids isolated from this library have been mapped across a panel of somatic cell hybrids, including the hybrids from the two patients, and have been localized to seven small regions of proximal 17q. We have 5 cosmids that map directly above the two NF1 translocations, and 11 cosmids that map directly below. Of these, 2 cosmids in each region are linked to the disease locus and 3 of these cosmids show no recombination. One distal cosmid, 2B/B35, detects the two NF1 translocations by pulsed-field gel analysis and has been used to produce a long-range restriction map that covers the translocations.

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Year:  1990        PMID: 2119504      PMCID: PMC54722          DOI: 10.1073/pnas.87.18.7255

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  29 in total

1.  A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion.

Authors:  B G Herrmann; D P Barlow; H Lehrach
Journal:  Cell       Date:  1987-03-13       Impact factor: 41.582

2.  Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene.

Authors:  B R Seizinger; G A Rouleau; L J Ozelius; A H Lane; A G Faryniarz; M V Chao; S Huson; B R Korf; D M Parry; M A Pericak-Vance
Journal:  Cell       Date:  1987-06-05       Impact factor: 41.582

3.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

4.  Removal of repeated sequences from hybridisation probes.

Authors:  P G Sealey; P A Whittaker; E M Southern
Journal:  Nucleic Acids Res       Date:  1985-03-25       Impact factor: 16.971

5.  A monoclonal antibody recognizing a cell surface antigen coded for by a gene on human chromosome 17.

Authors:  Y Bai; D Sheer; L Hiorns; R W Knowles; A Tunnacliffe
Journal:  Ann Hum Genet       Date:  1982-10       Impact factor: 1.670

6.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

7.  Neurofibromatosis in the South African Indian community--further evidence for heterogeneity?

Authors:  C E Wallis; C P Slater
Journal:  S Afr Med J       Date:  1987-10-03

8.  Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.

Authors:  D Barker; E Wright; K Nguyen; L Cannon; P Fain; D Goldgar; D T Bishop; J Carey; B Baty; J Kivlin
Journal:  Science       Date:  1987-05-29       Impact factor: 47.728

9.  Deletion of genes on chromosome 1 in endocrine neoplasia.

Authors:  C G Mathew; B A Smith; K Thorpe; Z Wong; N J Royle; A J Jeffreys; B A Ponder
Journal:  Nature       Date:  1987 Aug 6-12       Impact factor: 49.962

10.  Genetic analysis of the 15;17 chromosome translocation associated with acute promyelocytic leukemia.

Authors:  D Sheer; L R Hiorns; K F Stanley; P N Goodfellow; D M Swallow; S Povey; N Heisterkamp; J Groffen; J R Stephenson; E Solomon
Journal:  Proc Natl Acad Sci U S A       Date:  1983-08       Impact factor: 11.205

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  5 in total

1.  A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCA1).

Authors:  D M Black; H Nicolai; J Borrow; E Solomon
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

2.  Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism.

Authors:  L M Kayes; V M Riccardi; W Burke; R L Bennett; K Stephens
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

3.  A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene.

Authors:  M Stark; G Assum; W Krone
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

4.  The human vitronectin (complement S-protein) gene maps to the centromeric region of 17q.

Authors:  T M Fink; D E Jenne; P Lichter
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

5.  Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line.

Authors:  J E Reynolds; J A Fletcher; C H Lytle; L Nie; C C Morton; S R Diehl
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

  5 in total

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