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J M W van den Ouweland

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P B M de Andrade; Blanca Rubi; F Frigerio; J M W van den Ouweland; J Antonie Maassen; Pierre Maechler
Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function.
J Antonie Maassen; J M W van den Ouweland; M Losekoot; Herman H P J Lemkes
[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
J Antonie Maassen; Einar Van Essen; J M W van den Ouweland; Herman H P J Lemkes
Molecular and clinical aspects of mitochondrial diabetes mellitus.

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2006: P B M de Andrade; Blanca Rubi; F Frigerio; J M W van den Ouweland; J Antonie Maassen; Pierre Maechler
Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function.
Diabetologia 2006;49(8):1816-26.
2001: J Antonie Maassen; J M W van den Ouweland; M Losekoot; Herman H P J Lemkes
[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
Nederlands tijdschrift voor geneeskunde 2001;145(24):1153-4.
2001: J Antonie Maassen; Einar Van Essen; J M W van den Ouweland; Herman H P J Lemkes
Molecular and clinical aspects of mitochondrial diabetes mellitus.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2001;109(3):127-34.
2000: Einar Van Essen; Bart O Roep; L M 't Hart; JJ Jansen; J M W van den Ouweland; Herman H P J Lemkes; J Antonie Maassen
HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.
Diabetic medicine : a journal of the British Diabetic Association 2000;17(12):841-7.
2000: J M W van den Ouweland; J B C de Klerk; MP van de Corput; Roeland W Dirks; Anton K Raap; Hans R Scholte; Jan G M Huijmans; LM Hart; G Jan Bruining; J Antonie Maassen
Characterization of a novel mitochondrial DNA deletion in a patient with a variant of the Pearson marrow-pancreas syndrome.
European journal of human genetics : EJHG 2000;8(3):195-203.
1999: George M C Janssen; J Antonie Maassen; J M W van den Ouweland
The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate.
The Journal of biological chemistry 1999;274(42):29744-8.
1999: J M W van den Ouweland; Pierre Maechler; C B Wollheim; G Attardi; J Antonie Maassen
Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.
Diabetologia 1999;42(4):485-92.
1998: Tonnie Rijkers; J M W van den Ouweland; Bruno Morolli; A G Rolink; Willy M Baarends; Petra P H Van Sloun; Paul H M Lohman; Albert Pastink
Targeted inactivation of mouse RAD52 reduces homologous recombination but not resistance to ionizing radiation.
Molecular and cellular biology 1998;18(11):6423-9.
1998: J Antonie Maassen; JJ Jansen; J M W van den Ouweland; LM Hart; Einar Van Essen; Herman H P J Lemkes
[A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
Nederlands tijdschrift voor geneeskunde 1998;142(5):229-33.
1997: JJ Jansen; J Antonie Maassen; F J van der Woude; H A Lemmink; J M W van den Ouweland; L M t' Hart; H J Smeets; J A Bruijn; Herman H P J Lemkes
Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.
Journal of the American Society of Nephrology : JASN 1997;8(7):1118-24.
1997: J M W van den Ouweland; Tonnie Rijkers; Albert Pastink
Genomic characterization of the mouse homolog of the Saccharomyces cerevisiae recombination and double-strand break repair gene RAD52.
Mutation research 1997;383(2):125-35.
1997: J Antonie Maassen; J M W van den Ouweland; L M t Hart; Herman H P J Lemkes
Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 1997;29(2):50-5.
1997: MP van de Corput; J M W van den Ouweland; Roeland W Dirks; LM Hart; G Jan Bruining; J Antonie Maassen; Anton K Raap
Detection of mitochondrial DNA deletions in human skin fibroblasts of patients with Pearson's syndrome by two-color fluorescence in situ hybridization.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1997;45(1):55-61.
1996: J Antonie Maassen; J J Jansen; T Kadowaki; J M W van den Ouweland; L M 't Hart; Herman H P J Lemkes
The molecular basis and clinical characteristics of Maternally Inherited Diabetes and Deafness (MIDD), a recently recognized diabetic subtype.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 1996;104(3):205-11.
1995: Klaus-Dieter Gerbitz; J M W van den Ouweland; J Antonie Maassen; Michaela Jaksch
Mitochondrial diabetes mellitus: a review.
Biochimica et biophysica acta 1995;1271(1):253-60.
1995: J M W van den Ouweland; Klaus-Dieter Gerbitz; Herman H P J Lemkes; J Antonie Maassen
Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
Muscle & nerve. Supplement 1995;(3):S124-30.
1995: J M W van den Ouweland; Herman H P J Lemkes; Klaus-Dieter Gerbitz; J Antonie Maassen
Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
Muscle & nerve. Supplement 1995;3():S124-30.
1994: L M t Hart; Herman H P J Lemkes; Robert J Heine; R P Stolk; E J Feskens; J J Jansen; F E van der Does; Diederick Grobbee; D Kromhout; J M W van den Ouweland
Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands.
Diabetologia 1994;37(11):1169-70.
1994: J M W van den Ouweland; Herman H P J Lemkes; R C Trembath; R Ross; G Velho; D Cohen; P Froguel; J Antonie Maassen
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
Diabetes 1994;43(6):746-51.
1992: J M W van den Ouweland; Herman H P J Lemkes; W Ruitenbeek; L A Sandkuijl; M F de Vijlder; P A Struyvenberg; J J van de Kamp; J Antonie Maassen
Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
Nature genetics 1992;1(5):368-71.
1992: J M W van den Ouweland; G Jan Bruining; Dick Lindhout; J M Wit; B F Veldhuyzen; J Antonie Maassen
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.
Nucleic acids research 1992;20(4):679-82.
1991: J M W van den Ouweland; Herman H P J Lemkes; J Antonie Maassen
A rare mitochondrial DNA BstNI polymorphism in a family with type II diabetes.
Nucleic acids research 1991;19(8):1962.
1990: G C Angenent; J M W van den Ouweland; John F Bol
Susceptibility to virus infection of transgenic tobacco plants expressing structural and nonstructural genes of tobacco rattle virus.
Virology 1990;175(1):191-8.