't Hart LM - Search Results

1

Genetic association analysis of LARS2 with type 2 diabetes.

Reiling E, Jafar-Mohammadi B, van 't Riet E, Weedon MN, van Vliet-Ostaptchouk JV, Hansen T, Saxena R, van Haeften TW, Arp PA, Das S, Nijpels G, Groenewoud MJ, van Hove EC, Uitterlinden AG, Smit JW, Morris AD, Doney AS, Palmer CN, Guiducci C, Hattersley AT, Frayling TM, Pedersen O, Slagboom PE, Altshuler DM, Groop L, Romijn JA, Maassen JA, Hofker MH, Dekker JM, McCarthy MI, 't Hart LM. Reiling E, et al. Diabetologia. 2010 Jan;53(1):103-10. doi: 10.1007/s00125-009-1557-7. Epub 2009 Oct 22. Diabetologia. 2010. PMID: 19847392 Free PMC article.

2

Evaluation of the importance of maternal history of diabetes and of mitochondrial variation in the development of NIDDM.

McCarthy M, Cassell P, Tran T, Mathias L, 't Hart LM, Maassen JA, Snehalatha C, Ramachandran A, Viswanathan M, Hitman GA. McCarthy M, et al. Diabet Med. 1996 May;13(5):420-8. doi: 10.1002/(SICI)1096-9136(199605)13:5<420::AID-DIA97>3.0.CO;2-W. Diabet Med. 1996. PMID: 8737023

3

The molecular basis and clinical characteristics of Maternally Inherited Diabetes and Deafness (MIDD), a recently recognized diabetic subtype.

Maassen JA, Jansen JJ, Kadowaki T, van den Ouweland JM, 't Hart LM, Lemkes HH. Maassen JA, et al. Exp Clin Endocrinol Diabetes. 1996;104(3):205-11. doi: 10.1055/s-0029-1211444. Exp Clin Endocrinol Diabetes. 1996. PMID: 8817237 Review.

4

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging.

't Hart LM, Jansen JJ, Lemkes HH, de Knijff P, Maassen JA. 't Hart LM, et al. Hum Mutat. 1996;7(3):193-7. doi: 10.1002/(SICI)1098-1004(1996)7:3<193::AID-HUMU2>3.0.CO;2-C. Hum Mutat. 1996. PMID: 8829651

5

Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.

Maassen JA, van den Ouweland JM, t Hart LM, Lemkes HH. Maassen JA, et al. Horm Metab Res. 1997 Feb;29(2):50-5. doi: 10.1055/s-2007-978984. Horm Metab Res. 1997. PMID: 9105898 Review.

6

Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.

Jansen JJ, Maassen JA, van der Woude FJ, Lemmink HA, van den Ouweland JM, t' Hart LM, Smeets HJ, Bruijn JA, Lemkes HH. Jansen JJ, et al. J Am Soc Nephrol. 1997 Jul;8(7):1118-24. doi: 10.1681/ASN.V871118. J Am Soc Nephrol. 1997. PMID: 9219161

7

Altered beta-cell characteristics in impaired glucose tolerant carriers of a GAA trinucleotide repeat polymorphism in the frataxin gene.

t Hart LM, Ruige JB, Dekker JM, Stehouwer CD, Maassen JA, Heine RJ. t Hart LM, et al. Diabetes. 1999 Apr;48(4):924-6. doi: 10.2337/diabetes.48.4.924. Diabetes. 1999. PMID: 10102715

8

HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.

van Essen EH, Roep BO, 't Hart LM, Jansen JJ, Van den Ouweland JM, Lemkes HH, Maassen JA. van Essen EH, et al. Diabet Med. 2000 Dec;17(12):841-7. doi: 10.1046/j.1464-5491.2000.00379.x. Diabet Med. 2000. PMID: 11168326

9

Variations in insulin secretion in carriers of gene variants in IRS-1 and -2.

't Hart LM, Nijpels G, Dekker JM, Maassen JA, Heine RJ, van Haeften TW. 't Hart LM, et al. Diabetes. 2002 Mar;51(3):884-7. doi: 10.2337/diabetes.51.3.884. Diabetes. 2002. PMID: 11872698

10

A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness.

Maassen JA, Biberoglu S, 't Hart LM, Bakker E, de Knijff P. Maassen JA, et al. Arch Physiol Biochem. 2002 Jul;110(3):186-8. doi: 10.1076/apab.110.3.186.8294. Arch Physiol Biochem. 2002. PMID: 12221518

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