Literature DB >> 2437795

The human myelin-basic-protein gene: chromosomal localization and RFLP analysis.

J Kamholz, R Spielman, K Gogolin, W Modi, S O'Brien, R Lazzarini.   

Abstract

With a human myelin-basic-protein (MBP) cDNA used as a probe, the human MBP gene has been mapped to chromosome region 18q22-q23 by a combination of Southern hybridization to a panel of somatic-cell hybrid DNAs and in situ hybridization to metaphase chromosomes. Restriction-fragment-length polymorphisms (RFLPs) have also been identified with this probe in human DNA, by means of the restriction enzymes BamHI, PvuII, and PstI. In studies of informative families, the alleles of the BamHI and PvuII polymorphisms have been shown to segregate as Mendelian traits.

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Year:  1987        PMID： 2437795      PMCID： PMC1684086     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


  14 in total

1.  Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19.

Authors:  S Naylor; J M Lalouel; D J Shaw
Journal:  Cytogenet Cell Genet       Date:  1985

2.  Trisomy 18qter and trisomy mapping of chromosome 18.

Authors:  C Turleau; J de Grouchy
Journal:  Clin Genet       Date:  1977-12       Impact factor: 4.438

3.  A strategy to reveal high-frequency RFLPs along the human X chromosome.

Authors:  J Aldridge; L Kunkel; G Bruns; U Tantravahi; M Lalande; T Brewster; E Moreau; M Wilson; W Bromley; T Roderick
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

4.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

5.  Familial partial distal 18q (18q22-18q23) trisomy.

Authors:  A De Muelenaere; J P Fryns; H Van den Berghe
Journal:  Ann Genet       Date:  1981

6.  Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.

Authors:  M E Harper; G F Saunders
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

7.  Localization of the human myelin basic protein gene (MBP) to region 18q22----qter by in situ hybridization.

Authors:  D F Saxe; N Takahashi; L Hood; M I Simon
Journal:  Cytogenet Cell Genet       Date:  1985

8.  Cloning and characterization of the myelin basic protein gene from mouse: one gene can encode both 14 kd and 18.5 kd MBPs by alternate use of exons.

Authors:  N Takahashi; A Roach; D B Teplow; S B Prusiner; L Hood
Journal:  Cell       Date:  1985-08       Impact factor: 41.582

9.  Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders.

Authors:  H F Willard; J R Riordan
Journal:  Science       Date:  1985-11-22       Impact factor: 47.728

10.  Confirmation of the regional assignment of peptidase A (PEPA) to 18q23 by gene dosage studies.

Authors:  C Junien; J de Grouchy; C Turleau; F Serville
Journal:  Ann Genet       Date:  1980
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  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.  Mapping structural differences of the corpus callosum in individuals with 18q deletions using targetless regional spatial normalization.

Authors:  Peter Kochunov; Jack Lancaster; Jean Hardies; Paul M Thompson; Roger P Woods; Jannine D Cody; Daniel E Hale; Angela Laird; Peter T Fox
Journal:  Hum Brain Mapp       Date:  2005-04       Impact factor: 5.038

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.  A new deletion of 18q23 with few typical features of the 18q- syndrome.

Authors:  M Kohonen-Corish; G Strathdee; J Overhauser; T McDonald; V Jammu
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

Review 5.  Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Authors:  A D Kline; M E White; R Wapner; K Rojas; L G Biesecker; J Kamholz; E H Zackai; M Muenke; C I Scott; J Overhauser
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

6.  Myelination in children with partial deletions of chromosome 18q.

Authors:  Jack L Lancaster; Jannine D Cody; Trevor Andrews; L Jean Hardies; Daniel E Hale; Peter T Fox
Journal:  AJNR Am J Neuroradiol       Date:  2005-03       Impact factor: 3.825

7.  Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles.

Authors:  Jun Yi Wang; David Hessl; Christine Iwahashi; Katherine Cheung; Andrea Schneider; Randi J Hagerman; Paul J Hagerman; Susan M Rivera
Journal:  Neuroimage       Date:  2012-10-12       Impact factor: 6.556

8.  Benign focal epilepsy with onset in infancy in a patient with 18q-syndrome.

Authors:  Alberto Verrotti; Daniela Trotta; Carmela Salladini; Giovanna di Corcia; Francesco Chiarelli
Journal:  Childs Nerv Syst       Date:  2003-12-23       Impact factor: 1.475

9.  No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs.

Authors:  N W Wood; P Holmans; D Clayton; N Robertson; D A Compston
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-10       Impact factor: 10.154
  9 in total

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