Literature DB >> 2878412

XhoI polymorphism at the human pronatriodilatin (hPND) gene locus.

M Nemer, D Sirois, J Drouin.   

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Year:  1986        PMID： 2878412      PMCID： PMC311896          DOI： 10.1093/nar/14.21.8696

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


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  1 in total

1.  Gene structure of human cardiac hormone precursor, pronatriodilatin.

Authors:  M Nemer; M Chamberland; D Sirois; S Argentin; J Drouin; R A Dixon; R A Zivin; J H Condra
Journal:  Nature       Date:  1984 Dec 13-19       Impact factor: 49.962
  1 in total
  7 in total

1.  An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance.

Authors:  C Hayward; J Livingstone; S Holloway; W A Liston; D J Brock
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

2.  A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.

Authors:  N C Dracopoli; B Z Stanger; C Y Ito; K M Call; S E Lincoln; E S Lander; D E Housman
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

3.  NsiI and ScaI restriction fragment length polymorphisms at the atrial natriuretic peptides (ANP) gene locus.

Authors:  U Masharani; P F Nakashima; D W Lim; P M Frossard
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

4.  Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus.

Authors:  D G Bradley; G J Farrar; E M Sharp; P Kenna; M M Humphries; D J McConnell; S P Daiger; P McWilliam; P Humphries
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

5.  Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36.

Authors:  L A Cannon-Albright; D E Goldgar; E C Wright; A Turco; M Jost; L J Meyer; M Piepkorn; J J Zone; M H Skolnick
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

6.  Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique.

Authors:  B A Kaufman; P S White; T Steinbrueck; H Donis-Keller; G M Brodeur
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

7.  Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

Authors:  E Shin; S Fujita; K Takami; H Kurahashi; Y Kurita; T Kobayashi; T Mori; I Nishisho; S Takai
Journal:  Jpn J Cancer Res       Date:  1993-04
  7 in total

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