Literature DB >> 1677184

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).

M H Polymeropoulos1, H Xiao, D S Rath, C R Merril.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1677184      PMCID: PMC328418     

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


× No keyword cloud information.
  4 in total

1.  Dinucleotide repeat polymorphism at the D10S89 locus.

Authors:  J L Weber; P E May
Journal:  Nucleic Acids Res       Date:  1990-08-11       Impact factor: 16.971

2.  Structure of the human tyrosine hydroxylase gene: alternative splicing from a single gene accounts for generation of four mRNA types.

Authors:  K Kobayashi; N Kaneda; H Ichinose; F Kishi; A Nakazawa; Y Kurosawa; K Fujita; T Nagatsu
Journal:  J Biochem       Date:  1988-06       Impact factor: 3.387

Review 3.  Report of the committee on the genetic constitution of chromosome 11.

Authors:  C Junien; O W McBride
Journal:  Cytogenet Cell Genet       Date:  1989

4.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

  4 in total
  29 in total

1.  Comments on the paper by D. Li and L. He: meta-analysis shows association between the tryptophan hydroxylase (TPH) gene and schizophrenia.

Authors:  P G Sand
Journal:  Hum Genet       Date:  2007-11       Impact factor: 4.132

2.  A search for association between schizophrenia and dopamine-related alleles.

Authors:  E Jönsson; S Brené; T Geijer; L Terenius; A Tylec; M L Persson; G Sedvall
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1996       Impact factor: 5.270

3.  Individual identification of flood victims by DNA polymorphisms and autopsy findings.

Authors:  A Mannucci; L Casarino; G Bruni; A Lomi; F De Stefano
Journal:  Int J Legal Med       Date:  1995       Impact factor: 2.686

4.  Evidence of a long QT founder gene with varying phenotypic expression in South African families.

Authors:  T de Jager; C H Corbett; J C Badenhorst; P A Brink; V A Corfield
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

5.  French Caucasian population data obtained from fluorescently detected HUMvWFA31/A and HUMF13A01 short tandem repeat loci.

Authors:  F Rousselet; H Pfitzinger; P Mangin
Journal:  Int J Legal Med       Date:  1996       Impact factor: 2.686

6.  Statistical analysis of data for three British ethnic groups from a new STR multiplex.

Authors:  I W Evett; P D Gill; J A Lambert; N Oldroyd; R Frazier; S Watson; S Panchal; A Connolly; C Kimpton
Journal:  Int J Legal Med       Date:  1997       Impact factor: 2.686

7.  Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.

Authors:  A Nordenskjöld; F Hedborg; H Luthman; M Nordenskjöld
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

8.  Locus heterogeneity of autosomal dominant long QT syndrome.

Authors:  M Curran; D Atkinson; K Timothy; G M Vincent; A J Moss; M Leppert; M Keating
Journal:  J Clin Invest       Date:  1993-08       Impact factor: 14.808

9.  Uniparental disomy occurs infrequently in Wilms tumor patients.

Authors:  P Grundy; B Wilson; P Telzerow; W Zhou; M C Paterson
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

10.  Family studies of non-insulin-dependent diabetes mellitus in South Indians.

Authors:  M I McCarthy; G A Hitman; D C Shields; N E Morton; C Snehalatha; V Mohan; A Ramachandran; M Viswanathan
Journal:  Diabetologia       Date:  1994-12       Impact factor: 10.122

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.