Literature DB >> 7983779

[The detection of GLUT2 gene mutation by polymerase-chain reaction single stranded conformation polymorphism (PCR-SSCP) method].

T Miura1, Y Yamada, Y Someya, A Kubota, Y Seino.   

Abstract

The polymerase chain reaction-single stranded conformation Polymorphism (PCR-SSCP) procedure was applied to examine whether the mutation in the liver/islet glucose transporter (GLUT2) gene could be associated with non-insulin-dependent diabetes mellitus (NIDDM) in Japanese. Samples were processed through 30-40 cycles of 1 min denaturation at 94 degrees C, 1 min annealing at 55-68 degrees C for 1-2 min, extention at 72 degrees C for 1 min, and denaturation at 94 degrees C for 1 min. We identified a silent mutation in codon 479 for PheTTT/TTC.

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Year:  1994        PMID: 7983779

Source DB:  PubMed          Journal:  Nihon Rinsho        ISSN: 0047-1852


  1 in total

1.  No mutation in the SLC2A2 ( GLUT2) gene in a Turkish infant with Fanconi-Bickel syndrome.

Authors:  Esra Arun Ozer; Nejat Aksu; Erkan Uclar; Hakan Erdogan; Ali Rahmi Bakiler; Masahiko Tsuda; Emiko Kitasawa; Mahmut Coker; Erdener Ozer
Journal:  Pediatr Nephrol       Date:  2003-03-11       Impact factor: 3.714

  1 in total

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