Bianca Miterski
Overview
Explore the profile of Bianca Miterski including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
143
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0
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Recent Articles
1.
Zerres K, Arning L, Bockmann B, Purczeld A, Miterski B
Dtsch Med Wochenschr
. 2020 Jul;
145(18):1337-1346.
PMID: 32674188
Every year, about 60 000 people in Germany contract colo-rectal carcinoma. Hereditary factors are the cause in approx. 5 % and those affected often fall ill at a young age....
2.
Heinritz W, Huffmeier U, Strenge S, Miterski B, Zweier C, Leinung S, et al.
Ann Hum Genet
. 2009 Apr;
73(Pt 3):283-91.
PMID: 19344451
Mutations in either the EXT1 or EXT2 genes lead to Multiple Osteochondromas (MO), an autosomal dominantly inherited disorder. This is a report on clinical findings and results of molecular analyses...
3.
Vogler S, Goedde R, Miterski B, Gold R, Kroner A, Koczan D, et al.
J Mol Med (Berl)
. 2005 Jul;
83(10):806-11.
PMID: 16021520
Uncoupling protein 2 (UCP2) is a member of the mitochondrial proton transport family that uncouples proton entry to the mitochondria from ATP synthesis. UCP2 expression levels have been linked to...
4.
Miterski B, Drynda S, Boschow G, Klein W, Oppermann J, Kekow J, et al.
BMC Genet
. 2004 Mar;
5:2.
PMID: 15018649
Background: Rheumatoid arthritis (RA) and juvenile rheumatoid arthritis (JRA) are complex multifactorial diseases caused by environmental influences and an unknown number of predisposing genes. The present study was undertaken in...
5.
Bohringer S, Hardt C, Miterski B, Steland A, Epplen J
Eur J Hum Genet
. 2003 Aug;
11(8):573-84.
PMID: 12891377
New statistics are developed to gather the contribution of many alleles at different loci to common diseases. Both inferential and descriptive statistics are included in order to uncover epistatic effects...
6.
Goedde R, Sawcer S, Boehringer S, Miterski B, Sindern E, Haupts M, et al.
Hum Genet
. 2002 Sep;
111(3):270-7.
PMID: 12215840
Multiple sclerosis (MS) is a demyelinating disorder of the central nervous system with putative autoimmune aetiology and complex genetic background. Here, we report the results of a genome screen for...
7.
Miterski B, Epplen J, Gencik M
Cell Mol Biol (Noisy-le-grand)
. 2002 May;
48(3):331-41.
PMID: 12030439
The genetics of multifactorial diseases characterized by autoimmune phenomena are elusive so far. Yet, it is clear that the genetic contribution to a given clinically defined autoimmune disease entity is...
8.
Miterski B, Sindern E, Haupts M, Schimrigk S, Epplen J
BMC Med Genet
. 2002 May;
3:3.
PMID: 12028593
Background: Since contradictory results have been reported, we reanalysed the 77C-->G transition in exon 4 of the protein-tyrosine phosphatase receptor-type C (PTPRC also known as CD45) in a large cohort...
9.
Suzuki T, Li W, Zhang Q, Karim A, Novak E, Sviderskaya E, et al.
Nat Genet
. 2002 Feb;
30(3):321-4.
PMID: 11836498
Hermansky-Pudlak syndrome (HPS) is a disorder of organelle biogenesis in which oculocutaneous albinism, bleeding and pulmonary fibrosis result from defects of melanosomes, platelet dense granules and lysosomes. HPS is common...