Literature DB >> 2011543

Dinucleotide repeat polymorphism at the MAOA locus.

G C Black1, Z Y Chen, I W Craig, J F Powell.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1991        PMID： 2011543      PMCID： PMC333688          DOI： 10.1093/nar/19.3.689-a

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


× No keyword cloud information.
  2 in total

1.  Structural features of human monoamine oxidase A elucidated from cDNA and peptide sequences.

Authors:  Y P Hsu; W Weyler; S Chen; K B Sims; W B Rinehart; M C Utterback; J F Powell; X O Breakefield
Journal:  J Neurochem       Date:  1988-10       Impact factor: 5.372

2.  Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease.

Authors:  E R Levy; J F Powell; V J Buckle; Y P Hsu; X O Breakefield; I W Craig
Journal:  Genomics       Date:  1989-08       Impact factor: 5.736
  2 in total
  23 in total

1.  Dinucleotide repeat (TG)23 polymorphism in the MAOB gene.

Authors:  J Grimsby; K Chen; E J Devor; C R Cloninger; J C Shih
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

2.  Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.

Authors:  S Lindsay; D L Thiselton; J B Bateman; J T Ngo; R S Sparkes; M Coleman; K E Davies; S S Bhattacharya
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

3.  Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.

Authors:  F Martínez; M Tomás; J M Millán; A Fernández; F Palau; F Prieto
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

4.  X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

Authors:  M Lagerström-Fermér; M Sundvall; E Johnsen; G L Warne; S M Forrest; J D Zajac; A Rickards; D Ravine; U Landegren; U Pettersson
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

5.  Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON)

Authors:  V Juvonen; J Vilkki; P Aula; E Nikoskelainen; M L Savontaus
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

6.  Possible association between monoamine oxidase A gene and bipolar affective disorder.

Authors:  Y Kawada; M Hattori; X Y Dai; S Nanko
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

7.  Monoamine oxidase A gene and bipolar affective disorder.

Authors:  L C Lim; J F Powell; R Murray; M Gill
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

8.  Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family.

Authors:  F A Hol; M P Geurds; O Jensson; B C Hamel; G E Moore; R Newton; E C Mariman
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

9.  Structure of the human gene for monoamine oxidase type A.

Authors:  Z Y Chen; G S Hotamisligil; J K Huang; L Wen; D Ezzeddine; N Aydin-Muderrisoglu; J F Powell; R H Huang; X O Breakefield; I Craig
Journal:  Nucleic Acids Res       Date:  1991-08-25       Impact factor: 16.971

10.  Structure and promoter organization of the human monoamine oxidase A and B genes.

Authors:  J C Shih; J Grimsby; K Chen; Q S Zhu
Journal:  J Psychiatry Neurosci       Date:  1993-01       Impact factor: 6.186
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.