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J M van Den Ouweland

Showing results (1-10 of 19) with videos related to

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Nucleic Acids Research|April 25, 1991
A rare mitochondrial DNA BstNI polymorphism in a family with type II diabetesJ M van den Ouweland, H Lemkes, J A Maassen
Virology|March 1, 1990
Susceptibility to virus infection of transgenic tobacco plants expressing structural and nonstructural genes of tobacco rattle virusG C Angenent, J M Van den Ouweland, J F Bol
The Journal of Biological Chemistry|October 9, 1999
The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rateG M Janssen, J A Maassen, J M van Den Ouweland
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial diabetes mellitus: a reviewK D Gerbitz, J M van den Ouweland, J A Maassen, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 4, 2001
[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)]J A Maassen, J M van den Ouweland, M Losekoot, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 21, 2001
Molecular and clinical aspects of mitochondrial diabetes mellitusJ A Maassen, E van Essen, J M van den Ouweland, et al.
Muscle & Nerve. Supplement|January 1, 1995
Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutationJ M van den Ouweland, H H Lemkes, K D Gerbitz, et al.
Diabetologia|May 7, 1999
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 diseaseJ M van den Ouweland, P Maechler, C B Wollheim, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 1, 1997
Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNAJ A Maassen, J M van den Ouweland, L M t Hart, et al.
Nucleic Acids Research|February 25, 1992
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegiaJ M van den Ouweland, G J Bruining, D Lindhout, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|April 25, 1991
A rare mitochondrial DNA BstNI polymorphism in a family with type II diabetesJ M van den Ouweland, H Lemkes, J A Maassen
Virology|March 1, 1990
Susceptibility to virus infection of transgenic tobacco plants expressing structural and nonstructural genes of tobacco rattle virusG C Angenent, J M Van den Ouweland, J F Bol
The Journal of Biological Chemistry|October 9, 1999
The diabetes-associated 3243 mutation in the mitochondrial tRNA(Leu(UUR)) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rateG M Janssen, J A Maassen, J M van Den Ouweland
Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial diabetes mellitus: a reviewK D Gerbitz, J M van den Ouweland, J A Maassen, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 4, 2001
[From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)]J A Maassen, J M van den Ouweland, M Losekoot, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 21, 2001
Molecular and clinical aspects of mitochondrial diabetes mellitusJ A Maassen, E van Essen, J M van den Ouweland, et al.
Muscle & Nerve. Supplement|January 1, 1995
Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutationJ M van den Ouweland, H H Lemkes, K D Gerbitz, et al.
Diabetologia|May 7, 1999
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 diseaseJ M van den Ouweland, P Maechler, C B Wollheim, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 1, 1997
Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNAJ A Maassen, J M van den Ouweland, L M t Hart, et al.
Nucleic Acids Research|February 25, 1992
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegiaJ M van den Ouweland, G J Bruining, D Lindhout, et al.
Pageof 2