Literature DB >> 9121700

Assignment of Alzheimer's presenilin-2 (PS-2) gene to 1q42.1 by fluorescence in situ hybridization.

T Takano1, N Sahara, Y Yamanouchi, H Mori.   

Abstract

Presenilin-2 (PS-2) was suggested to be localized on 1q31-42 based on linkage analysis and cDNA cloning. The final identification of PS-2 as the causal gene for early-onset familial Alzheimer's disease in Voga-German pedigrees was concluded based on the point mutation found in the candidate cDNA isolated from this familial AD. We present evidence of its physical genome mapping of PS-2 on chromosome 1q42.1 by fluorescence in situ hybridization method.

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Year:  1997        PMID: 9121700     DOI: 10.1016/s0304-3940(96)13290-0

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  2 in total

1.  De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

Authors:  C Dumanchin; A Brice; D Campion; D Hannequin; C Martin; V Moreau; Y Agid; M Martinez; F Clerget-Darpoux; T Frebourg
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

Review 2.  Fish-on-a-chip: a sensitive detection microfluidic system for Alzheimer's disease.

Authors:  Jasmine P Devadhasan; Sanghyo Kim; Jeongho An
Journal:  J Biomed Sci       Date:  2011-05-28       Impact factor: 8.410

  2 in total

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