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Stefanie Zanssen

Research Profile

Chemicals & Drugs

Disorders

Procedures

Anatomy

Muscle Mitochondrion

Physiology

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Molecular Sequence Data

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Publications

TOP 3
Stefanie Zanssen; Eric A Schon
Mitochondrial DNA mutations in cancer.
Bjoern Linnartz; Roswitha Anglmayer; Stefanie Zanssen
Comprehensive scanning of somatic mitochondrial DNA alterations in acute leukemia developing from myelodysplastic syndromes.
Stefanie Zanssen; Bastian Gunawan; Laszlo Fuzesi; Dorothy Warburton; Eric A Schon
Renal oncocytomas with rearrangements involving 11q13 contain breakpoints near CCND1.

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All Publications

2005: Stefanie Zanssen; Eric A Schon
Mitochondrial DNA mutations in cancer.
PLoS medicine 2005;2(11):e401.
2004: Bjoern Linnartz; Roswitha Anglmayer; Stefanie Zanssen
Comprehensive scanning of somatic mitochondrial DNA alterations in acute leukemia developing from myelodysplastic syndromes.
Cancer research 2004;64(6):1966-71.
2004: Stefanie Zanssen; Bastian Gunawan; Laszlo Fuzesi; Dorothy Warburton; Eric A Schon
Renal oncocytomas with rearrangements involving 11q13 contain breakpoints near CCND1.
Cancer genetics and cytogenetics 2004;149(2):120-4.
2004: Stefanie Zanssen
Single cell PCR from archival stained bone marrow slides: a method for molecular diagnosis and characterization.
Journal of clinical laboratory analysis 2004;18(3):176-81.
2003: Stefanie Zanssen; Gerhard Buse
Successful chemotherapy in a male patient with malignant lymphoma and Leber's hereditary optic neuropathy (LHON).
American journal of hematology 2003;72(4):263-6.
2000: C Bank; Tewfik Soulimane; J Michael Schröder; Gerhard Buse; Stefanie Zanssen
Multiple deletions of mtDNA remove the light strand origin of replication.
Biochemical and biophysical research communications 2000;279(2):595-601.
2000: Stefanie Zanssen; Mária Judit Molnár; Gerhard Buse; J Michael Schröder
Novel cluster of tRNALeu(UUR) mutations in a sporadic case of infantile myopathy restricted to muscle tissue.
Neuropediatrics 2000;31(2):93-6.
1998: Stefanie Zanssen; Mária Judit Molnár; Gerhard Buse; J Michael Schröder
Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
Clinical neuropathology 1998;17(6):291-6.
1997: Stefanie Zanssen; Mária Judit Molnár; J Michael Schröder; Gerhard Buse
Multiple mitochondrial tRNA(Leu[UUR]) mutations associated with infantile myopathy.
Molecular and cellular biochemistry 1997;174(1-2):231-6.
1996: Mária Judit Molnár; Stefanie Zanssen; Gerhard Buse; J Michael Schröder
A large-scale deletion of mitochondrial DNA in a case with pure mitochondrial myopathy and neuropathy.
Acta neuropathologica 1996;91(6):654-8.

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