Hart LM - Search Results

1

An insulin receptor mutant (Asp707 --> Ala), involved in leprechaunism, is processed and transported to the cell surface but unable to bind insulin.

Hart LM, Lindhout D, Van der Zon GC, Kayserilli H, Apak MY, Kleijer WJ, Van der Vorm ER, Maassen JA. Hart LM, et al. J Biol Chem. 1996 Aug 2;271(31):18719-24. doi: 10.1074/jbc.271.31.18719. J Biol Chem. 1996. PMID: 8702527 Free article.

2

Absence of the Gly40-Ser mutation in the glucagon receptor among diabetic patients in the Netherlands.

Hart LM, Stolk RP, Jansen JJ, Grobbee DE, Lemkes HH, Maassen JA. Hart LM, et al. Diabetes Care. 1995 Oct;18(10):1400-1. doi: 10.2337/diacare.18.10.1400. Diabetes Care. 1995. PMID: 8721949 No abstract available.

3

Association of the insulin-receptor variant Met-985 with hyperglycemia and non-insulin-dependent diabetes mellitus in the Netherlands: a population-based study.

Hart LM, Stolk RP, Heine RJ, Grobbee DE, van der Does FE, Maassen JA. Hart LM, et al. Am J Hum Genet. 1996 Nov;59(5):1119-25. Am J Hum Genet. 1996. PMID: 8900242 Free PMC article. Clinical Trial.

4

Detection of mitochondrial DNA deletions in human skin fibroblasts of patients with Pearson's syndrome by two-color fluorescence in situ hybridization.

van de Corput MP, van den Ouweland JM, Dirks RW, Hart LM, Bruining GJ, Maassen JA, Raap AK. van de Corput MP, et al. Among authors: hart lm. J Histochem Cytochem. 1997 Jan;45(1):55-61. doi: 10.1177/002215549704500108. J Histochem Cytochem. 1997. PMID: 9010469

5

[A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].

Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH. Maassen JA, et al. Among authors: hart lm. Ned Tijdschr Geneeskd. 1998 Jan 31;142(5):229-33. Ned Tijdschr Geneeskd. 1998. PMID: 9557035 Dutch.

6

Prevalence of variants in candidate genes for type 2 diabetes mellitus in The Netherlands: the Rotterdam study and the Hoorn study.

Hart LM, Stolk RP, Dekker JM, Nijpels G, Grobbee DE, Heine RJ, Maassen JA. Hart LM, et al. J Clin Endocrinol Metab. 1999 Mar;84(3):1002-6. doi: 10.1210/jcem.84.3.5563. J Clin Endocrinol Metab. 1999. PMID: 10084586

7

Search for mitochondrial DNA mutations in migraine subgroups.

Haan J, Terwindt GM, Maassen JA, Hart LM, Frants RR, Ferrari MD. Haan J, et al. Among authors: hart lm. Cephalalgia. 1999 Jan;19(1):20-2. doi: 10.1111/j.1468-2982.1999.1901020.x. Cephalalgia. 1999. PMID: 10099855 Clinical Trial.

8

Variants in the sulphonylurea receptor gene: association of the exon 16-3t variant with Type II diabetes mellitus in Dutch Caucasians.

Hart LM, de Knijff P, Dekker JM, Stolk RP, Nijpels G, van der Does FE, Ruige JB, Grobbee DE, Heine RJ, Maassen JA. Hart LM, et al. Diabetologia. 1999 May;42(5):617-20. doi: 10.1007/s001250051203. Diabetologia. 1999. PMID: 10333056

9

Characterization of a novel mitochondrial DNA deletion in a patient with a variant of the Pearson marrow-pancreas syndrome.

van den Ouweland JM, de Klerk JB, van de Corput MP, Dirks RW, Raap AK, Scholte HR, Huijmans JG, Hart LM, Bruining GJ, Maassen JA. van den Ouweland JM, et al. Among authors: hart lm. Eur J Hum Genet. 2000 Mar;8(3):195-203. doi: 10.1038/sj.ejhg.5200444. Eur J Hum Genet. 2000. PMID: 10780785

10

Reduced second phase insulin secretion in carriers of a sulphonylurea receptor gene variant associating with Type II diabetes mellitus.

Hart LM, Dekker JM, van Haeften TW, Ruige JB, Stehouwer CD, Erkelens DW, Heine RJ, Maassen JA. Hart LM, et al. Diabetologia. 2000 Apr;43(4):515-9. doi: 10.1007/s001250051337. Diabetologia. 2000. PMID: 10819247

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

211 results

Search Page

Filters