Literature DB >> 19573128

Mutations in MAFA and IAPP are not a common cause of monogenic diabetes.

I Garin, R Martinez, J de las Heras, G Perez-Nanclares, L Castano, G Perez de Nanclares.   

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Year:  2009        PMID： 19573128     DOI： 10.1111/j.1464-5491.2009.02758.x

Source DB:  PubMed          Journal:  Diabet Med        ISSN： 0742-3071            Impact factor:   4.359


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  3 in total

1.  The embryonic transcription factor Hlxb9 is a menin interacting partner that controls pancreatic β-cell proliferation and the expression of insulin regulators.

Authors:  Kerong Shi; Vaishali I Parekh; Swarnava Roy; Shruti S Desai; Sunita K Agarwal
Journal:  Endocr Relat Cancer       Date:  2013-02-18       Impact factor: 5.678

2.  Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study.

Authors:  Robert Y L Zee; Patricia Pulido-Perez; Ricardo Perez-Fuentes; Paul M Ridker; Daniel I Chasman; Jose R Romero
Journal:  Clin Chim Acta       Date:  2011-01-08       Impact factor: 3.786

3.  MAFA missense mutation causes familial insulinomatosis and diabetes mellitus.

Authors:  Donato Iacovazzo; Sarah E Flanagan; Emily Walker; Rosana Quezado; Fernando Antonio de Sousa Barros; Richard Caswell; Matthew B Johnson; Matthew Wakeling; Michael Brändle; Min Guo; Mary N Dang; Plamena Gabrovska; Bruno Niederle; Emanuel Christ; Stefan Jenni; Bence Sipos; Maike Nieser; Andrea Frilling; Ketan Dhatariya; Philippe Chanson; Wouter W de Herder; Björn Konukiewitz; Günter Klöppel; Roland Stein; Márta Korbonits; Sian Ellard
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-16       Impact factor: 11.205
  3 in total

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