Lindhout D - Search Results

1

A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance.

Klinkhamer MP, Groen NA, van der Zon GC, Lindhout D, Sandkuyl LA, Krans HM, Möller W, Maassen JA. Klinkhamer MP, et al. Among authors: lindhout d. EMBO J. 1989 Sep;8(9):2503-7. doi: 10.1002/j.1460-2075.1989.tb08387.x. EMBO J. 1989. PMID: 2479553 Free PMC article.

2

Individuals with only one allele for a functional insulin receptor have a tendency to hyperinsulinaemia but not to hyperglycaemia.

Lekanne Deprez RH, Potter van Loon BJ, van der Zon GC, Möller W, Lindhout D, Klinkhamer MP, Krans HM, Maassen JA. Lekanne Deprez RH, et al. Among authors: lindhout d. Diabetologia. 1989 Oct;32(10):740-4. doi: 10.1007/BF00274534. Diabetologia. 1989. PMID: 2687060

3

Fibroblasts from a leprechaun patient have defects in insulin binding and insulin receptor autophosphorylation.

Maassen JA, Klinkhamer MP, van der Zon GC, Sips H, Möller W, Krans HM, Lindhout D, Beemer FA. Maassen JA, et al. Among authors: lindhout d. Diabetologia. 1988 Aug;31(8):612-7. doi: 10.1007/BF00264769. Diabetologia. 1988. PMID: 2851471

4

An Arg for Gly substitution at position 31 in the insulin receptor, linked to insulin resistance, inhibits receptor processing and transport.

van der Vorm ER, van der Zon GC, Möller W, Krans HM, Lindhout D, Maassen JA. van der Vorm ER, et al. Among authors: lindhout d. J Biol Chem. 1992 Jan 5;267(1):66-71. J Biol Chem. 1992. PMID: 1730625 Free article.

5

Prenatal analysis of insulin receptor autophosphorylation in a family with leprechaunism.

Maassen JA, Lindhout D, Reuss A, Kleijer WJ. Maassen JA, et al. Among authors: lindhout d. Prenat Diagn. 1990 Jan;10(1):13-6. doi: 10.1002/pd.1970100103. Prenat Diagn. 1990. PMID: 2315274

6

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. Among authors: lindhout d. 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.

7

[Molecular heterogeneity of congenital forms of insulin resistance].

van der Vorm ER, Lindhout D, Wit JM, Odink RJ, Krans HM, Maassen JA. van der Vorm ER, et al. Among authors: lindhout d. Ned Tijdschr Geneeskd. 1991 Jun 29;135(26):1165-70. Ned Tijdschr Geneeskd. 1991. PMID: 1650430 Dutch. No abstract available.

8

Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.

van den Ouweland JM, Bruining GJ, Lindhout D, Wit JM, Veldhuyzen BF, Maassen JA. van den Ouweland JM, et al. Among authors: lindhout d. Nucleic Acids Res. 1992 Feb 25;20(4):679-82. doi: 10.1093/nar/20.4.679. Nucleic Acids Res. 1992. PMID: 1542564 Free PMC article.

9

Is familial hemiplegic migraine a hereditary form of basilar migraine?

Haan J, Terwindt GM, Ophoff RA, Bos PL, Frants RR, Ferrari MD, Krommenhoek T, Lindhout DL, Sandkuyl LA, Van Eyk R. Haan J, et al. Among authors: lindhout dl. Cephalalgia. 1995 Dec;15(6):477-81. doi: 10.1046/j.1468-2982.1995.1506477.x. Cephalalgia. 1995. PMID: 8706110 Clinical Trial.

10

Genetic heterogeneity in tuberous sclerosis.

Janssen LA, Sandkuyl LA, Merkens EC, Maat-Kievit JA, Sampson JR, Fleury P, Hennekam RC, Grosveld GC, Lindhout D, Halley DJ. Janssen LA, et al. Among authors: lindhout d. Genomics. 1990 Oct;8(2):237-42. doi: 10.1016/0888-7543(90)90277-2. Genomics. 1990. PMID: 1979047

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