Christine Schwienbacher
Center for Biomedicine
European Academy Bozen/Bolzano (EURAC)
Christine Schwienbacher has not added Biography.
If you are Christine Schwienbacher and would like to personalize this page please email our Author Liaison for assistance.
Loss of methylation at chromosome 11p15.5 is common in human adult tumors.
Oncogene Apr, 2002 | Pubmed ID: 11971191
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15).
Blood May, 2002 | Pubmed ID: 11986249
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
Human molecular genetics Feb, 2007 | Pubmed ID: 17158821
Genetic determinants of circulating sphingolipid concentrations in European populations.
PLoS genetics Oct, 2009 | Pubmed ID: 19798445
Copy number variation and association over T-cell receptor genes--influence of DNA source.
Immunogenetics Aug, 2010 | Pubmed ID: 20582410
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
Nature genetics Dec, 2010 | Pubmed ID: 21076409
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.
Human molecular genetics Mar, 2011 | Pubmed ID: 21149283
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.
Human molecular genetics Mar, 2011 | Pubmed ID: 21208937
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
American journal of human genetics Jul, 2012 | Pubmed ID: 22703881
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
American journal of human genetics Oct, 2012 | Pubmed ID: 23022100
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes.
Journal of molecular neuroscience : MN Mar, 2013 | Pubmed ID: 23054586
SNP prioritization using a Bayesian probability of association.
Genetic epidemiology Feb, 2013 | Pubmed ID: 23280596
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.
Genetic epidemiology Feb, 2013 | Pubmed ID: 23307621
Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasis.
Hepatology (Baltimore, Md.) Nov, 2013 | Pubmed ID: 23504908
Profiling of Parkin-binding partners using tandem affinity purification.
PloS one , 2013 | Pubmed ID: 24244333
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies.
BMC endocrine disorders , 2014 | Pubmed ID: 24484869
Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson's disease blood samples.
BMC research notes , 2014 | Pubmed ID: 25304816
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Nature communications , 2014 | Pubmed ID: 25352340
Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PD.
Neurology Feb, 2015 | Pubmed ID: 25596505
Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Nature communications , 2015 | Pubmed ID: 25817829
Generation of Induced Pluripotent Stem Cells from Frozen Buffy Coats using Non-integrating Episomal Plasmids
JoVE 소개
Copyright © 2024 MyJoVE Corporation. 판권 소유