Literature DB >> 7901716

Prevalence of mitochondrial gene mutations in families with diabetes mellitus.

N Vionnet, P Passa, P Froguel.   

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Year:  1993        PMID： 7901716     DOI： 10.1016/0140-6736(93)92792-r

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  9 in total

1.  Non-isotopic and sensitive method for diagnosis of maternally-inherited diabetes and deafness.

Authors:  H Blanché; P Froguel; J Dausset; D Cohen; N Cohen
Journal:  Diabetologia       Date:  1994-08       Impact factor: 10.122

2.  Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation.

Authors:  Ayman W El-Hattab; Lisa T Emrick; Jean W Hsu; Sirisak Chanprasert; Farook Jahoor; Fernando Scaglia; William J Craigen
Journal:  Mitochondrion       Date:  2014-07-30       Impact factor: 4.160

3.  Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).

Authors:  S Suzuki; Y Hinokio; S Hirai; M Onoda; M Matsumoto; M Ohtomo; H Kawasaki; Y Satoh; H Akai; K Abe
Journal:  Diabetologia       Date:  1994-08       Impact factor: 10.122

4.  Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands.

Authors:  L M t Hart; H H Lemkes; R J Heine; R P Stolk; E J Feskens; J J Jansen; F E van der Does; D E Grobbee; D Kromhout; J M van den Ouweland
Journal:  Diabetologia       Date:  1994-11       Impact factor: 10.122

5.  Rapid Detection of the mt3243A > G Mutation Using Urine Sediment in Elderly Chinese Type 2 Diabetic Patients.

Authors:  Yinan Zhang; Xiujuan Du; Xinqian Geng; Chen Chu; Huijuan Lu; Yixie Shen; Ruihua Chen; Pingyan Fang; Yanmei Feng; Xiaojie Zhang; Yan Chen; Yanping Zhou; Congrong Wang; Weiping Jia
Journal:  J Diabetes Res       Date:  2017-06-21       Impact factor: 4.011

Review 6.  Significance of taurine transporter (TauT) in homeostasis and its layers of regulation (Review).

Authors:  Stella Baliou; Anthony M Kyriakopoulos; Maria Goulielmaki; Michalis I Panayiotidis; Demetrios A Spandidos; Vassilios Zoumpourlis
Journal:  Mol Med Rep       Date:  2020-07-09       Impact factor: 2.952

7.  Mitochondrial mutation m.3243A>G associates with insulin resistance in non-diabetic carriers.

Authors:  Jakob Høgild Langdahl; Anja Lisbeth Frederiksen; John Vissing; Morten Frost; Knud Bonnet Yderstræde; Per Heden Andersen
Journal:  Endocr Connect       Date:  2019-07       Impact factor: 3.335

8.  Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence.

Authors:  P P Rath; S Jenkins; M Michaelides; A Smith; M G Sweeney; M B Davis; F W Fitzke; A C Bird
Journal:  Br J Ophthalmol       Date:  2008-05       Impact factor: 4.638

Review 9.  Endocrine disorders in mitochondrial disease.

Authors:  Andrew M Schaefer; Mark Walker; Douglass M Turnbull; Robert W Taylor
Journal:  Mol Cell Endocrinol       Date:  2013-06-13       Impact factor: 4.102
  9 in total

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