Kết quả tìm kiếm - Simone Rost
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1
Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment Bằng Matthias Watzka, Christof Geisen, Carville G. Bevans, Katja Sittinger, Gabriele Spohn, Simone Rost, E. Seifried, C. R. Müller, Johannes Oldenburg
Được phát hành 2010Artigo -
2
Panel Sequencing Shows Recurrent Genetic FAS Alterations in Primary Cutaneous Marginal Zone Lymphoma Bằng Katja Maurus, Silke Appenzeller, Sabine Roth, Jochen Kuper, Simone Rost, Svenja Meierjohann, Panagiota Arampatzi, Matthias Goebeler, Andreas Rosenwald, Eva Geissinger, Marion Wobser
Được phát hành 2018Artigo -
3
Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1 Bằng Mirjam Larsen, Simone Rost, Nady El Hajj, A. Ferbert, Marcus Deschauer, Maggie C. Walter, Benedikt Schoser, Paweł Tacik, Wolfram Kreß, Clemens R. Müller
Được phát hành 2014Artigo -
4
Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin? Bằng Simone Rost, Hans‐Joachim Pelz, Sandra Menzel, Alan D. MacNicoll, Vanina León, Ki-Joon Song, Thomas Jäkel, Johannes Oldenburg, Clemens R. Müller
Được phát hành 2009Artigo -
5
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6 Bằng Simone Rost, Elisa Bach, Cordula Neuner, Indrajit Nanda, Sandra Dysek, Reginald E. Bittner, Alexander Keller, Oliver Bartsch, Robert Mlynski, Thomas Haaf, Clemens R. Müller, Erdmute Kunstmann
Được phát hành 2013Artigo -
6
Paternal age effects on sperm<i>FOXK1</i>and<i>KCNA7</i>methylation and transmission into the next generation Bằng Stefanie Atsem, Juliane Reichenbach, Ramya Potabattula, Marcus Dittrich, Caroline Nava, Christel Depienne, Lena Böhm, Simone Rost, Thomas von Hahn, Martin Schorsch, Thomas Haaf, Nady El Hajj
Được phát hành 2016Artigo -
7
Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication Bằng Juliane Lippert, Silke Appenzeller, Raimunde Liang, Silviu Sbiera, Stefan Kircher, Barbara Altieri, Indrajit Nanda, Isabel Weigand, Andrea Gehrig, Sonja Steinhauer, Renzo J. M. Riemens, Andreas Rosenwald, Clemens R. Müller, Matthias Kroiß, Simone Rost, Martin Faßnacht, Cristina L. Ronchi
Được phát hành 2018Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Genetics
Gene
Medicine
Missense mutation
Mutation
CYP2C9
Cancer research
DNA methylation
Gene expression
Genotype
Methylation
VKORC1
Vitamin K epoxide reductase
Adrenocortical carcinoma
Allele
Alport syndrome
Andrology
Antibody
Astronomy
Audiology
Autism
B cell
Bioinformatics
Complementary DNA
Compound heterozygosity
Context (archaeology)
Cord blood
Epigenetics
Epigenome