Literature DB >> 7894176

Genetic mapping of the glycine receptor alpha 3 subunit on mouse chromosome 8.

S F Kingsmore1, D Suh, M F Seldin.   

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Year:  1994        PMID： 7894176     DOI： 10.1007/bf00292030

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  7 in total

1.  A linkage map of mouse chromosome 8: further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19.

Authors:  T A Howard; J M Rochelle; A M Saunders; M F Seldin
Journal:  Genomics       Date:  1991-05       Impact factor: 5.736

2.  Identification and functional expression of a novel ligand binding subunit of the inhibitory glycine receptor.

Authors:  J Kuhse; V Schmieden; H Betz
Journal:  J Biol Chem       Date:  1990-12-25       Impact factor: 5.157

3.  Isolation and sequence analysis of cDNA for rat carboxypeptidase E [EC 3.4.17.10], a neuropeptide processing enzyme.

Authors:  L D Fricker; J P Adelman; J Douglass; R C Thompson; R P von Strandmann; J Hutton
Journal:  Mol Endocrinol       Date:  1989-04

4.  Retinal degeneration in the nervous mutant mouse. II. Electron microscopic analysis.

Authors:  M P White; G M Gorrin; R J Mullen; M M LaVail
Journal:  J Comp Neurol       Date:  1993-07-08       Impact factor: 3.215

5.  Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion.

Authors:  S F Kingsmore; B Giros; D Suh; M Bieniarz; M G Caron; M F Seldin
Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

6.  Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 8.

Authors:  J D Ceci
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

7.  Widespread expression of glycine receptor subunit mRNAs in the adult and developing rat brain.

Authors:  M L Malosio; B Marquèze-Pouey; J Kuhse; H Betz
Journal:  EMBO J       Date:  1991-09       Impact factor: 11.598
  7 in total
  3 in total

1.  Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.

Authors:  Tahir N Khan; Kamal Khan; Azita Sadeghpour; Hannah Reynolds; Yezmin Perilla; Marie T McDonald; William B Gallentine; Shahid M Baig; Erica E Davis; Nicholas Katsanis
Journal:  Am J Hum Genet       Date:  2019-01-03       Impact factor: 11.025

2.  Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes.

Authors:  Niina Sandholm; Carol Forsblom; Ville-Petteri Mäkinen; Amy Jayne McKnight; Anne-May Osterholm; Bing He; Valma Harjutsalo; Raija Lithovius; Daniel Gordin; Maija Parkkonen; Markku Saraheimo; Lena M Thorn; Nina Tolonen; Johan Wadén; Jaakko Tuomilehto; Maria Lajer; Emma Ahlqvist; Anna Möllsten; M Loredana Marcovecchio; Jason Cooper; David Dunger; Andrew D Paterson; Gianpaolo Zerbini; Leif Groop; Lise Tarnow; Alexander P Maxwell; Karl Tryggvason; Per-Henrik Groop
Journal:  Diabetologia       Date:  2014-03-05       Impact factor: 10.122

3.  Novel GLRA1 missense mutation (P250T) in dominant hyperekplexia defines an intracellular determinant of glycine receptor channel gating.

Authors:  B Saul; T Kuner; D Sobetzko; W Brune; F Hanefeld; H M Meinck; C M Becker
Journal:  J Neurosci       Date:  1999-02-01       Impact factor: 6.167
  3 in total

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