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Matthias Schwab
Matthias Schwab
Altri nomiSchwab M
Dr Margarete Fischer-Bosch Inst.of Clin.Pharmacol.,Stuttgart+Dept.Clin.Pharmacol.Univ.Hosp.Tübingen
Email verificata su ikp-stuttgart.de - Home page
Titolo
Citata da
Citata da
Anno
Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation
UM Zanger, M Schwab
Pharmacology & therapeutics 138 (1), 103-141, 2013
42682013
Metformin improves healthspan and lifespan in mice
A Martin-Montalvo, EM Mercken, SJ Mitchell, HH Palacios, PL Mote, ...
Nature communications 4 (1), 2192, 2013
15022013
Reduced Paneth cell α-defensins in ileal Crohn's disease
J Wehkamp, NH Salzman, E Porter, S Nuding, M Weichenthal, RE Petras, ...
Proceedings of the National Academy of Sciences 102 (50), 18129-18134, 2005
13262005
NOD2 (CARD15) mutations in Crohn’s disease are associated with diminished mucosal α-defensin expression
J Wehkamp, J Harder, M Weichenthal, M Schwab, E Schäffeler, M Schlee, ...
Gut 53 (11), 1658-1664, 2004
11442004
Frequency of single nucleotide polymorphisms in the P‐glycoprotein drug transporter MDR1 gene in white subjects
I Cascorbi, T Gerloff, A Johne, C Meisel, S Hoffmeyer, M Schwab, ...
Clinical Pharmacology & Therapeutics 69 (3), 169-174, 2001
9342001
A new molecular predictor of distant recurrence in ER-positive, HER2-negative breast cancer adds independent information to conventional clinical risk factors
M Filipits, M Rudas, R Jakesz, P Dubsky, F Fitzal, CF Singer, O Dietze, ...
Clinical Cancer Research 17 (18), 6012-6020, 2011
8012011
Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation
UM Zanger, M Turpeinen, K Klein, M Schwab
Analytical and bioanalytical chemistry 392, 1093-1108, 2008
7592008
A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon
K Fellermann, DE Stange, E Schaeffeler, H Schmalzl, J Wehkamp, ...
The American Journal of Human Genetics 79 (3), 439-448, 2006
7182006
Extensive genetic polymorphism in the human CYP2B6 gene with impact on expression and function in human liver
T Lang, K Klein, J Fischer, AK Nüssler, P Neuhaus, U Hofmann, ...
Pharmacogenetics and Genomics 11 (5), 399-415, 2001
7122001
Association between CYP2D6 polymorphisms and outcomes among women with early stage breast cancer treated with tamoxifen
W Schroth, MP Goetz, U Hamann, PA Fasching, M Schmidt, S Winter, ...
Jama 302 (13), 1429-1436, 2009
6632009
Sex is a major determinant of CYP3A4 expression in human liver
R Wolbold, K Klein, O Burk, AK Nüssler, P Neuhaus, M Eichelbaum, ...
Hepatology 38 (4), 978-988, 2003
6192003
Breast cancer treatment outcome with adjuvant tamoxifen relative to patient CYP2D6 and CYP2C19 genotypes
W Schroth, L Antoniadou, P Fritz, M Schwab, T Muerdter, UM Zanger, ...
Journal of Clinical Oncology 25 (33), 5187-5193, 2007
6002007
Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for dihydropyrimidine dehydrogenase genotype and fluoropyrimidine dosing: 2017 update
U Amstutz, LM Henricks, SM Offer, J Barbarino, JHM Schellens, JJ Swen, ...
Clinical Pharmacology & Therapeutics 103 (2), 210-216, 2018
5962018
Clinical Pharmacogenetics Implementation Consortium Guideline for Thiopurine Dosing Based on TPMT and NUDT15 Genotypes: 2018 Update
MV Relling, M Schwab, M Whirl‐Carrillo, G Suarez‐Kurtz, CH Pui, ...
Clinical Pharmacology & Therapeutics 105 (5), 1095-1105, 2019
5822019
Comprehensive analysis of thiopurine S-methyltransferase phenotype–genotype correlation in a large population of German-Caucasians and identification of novel TPMT variants
E Schaeffeler, C Fischer, D Brockmeier, D Wernet, K Moerike, ...
Pharmacogenetics and Genomics 14 (7), 407-417, 2004
5242004
High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)
M Niemi, E Schaeffeler, T Lang, MF Fromm, M Neuvonen, C Kyrklund, ...
Pharmacogenetics and Genomics 14 (7), 429-440, 2004
5162004
The C3435T mutation in the human MDR1 gene is associated with altered efflux of the P-glycoprotein substrate rhodamine 123 from CD56+ natural killer cells
M Hitzl, S Drescher, H van der Kuip, E Schäffeler, J Fischer, M Schwab, ...
Pharmacogenetics and Genomics 11 (4), 293-298, 2001
5152001
Role of genetic and nongenetic factors for fluorouracil treatment-related severe toxicity: a prospective clinical trial by the German 5-FU Toxicity Study Group
M Schwab, UM Zanger, C Marx, E Schaeffeler, K Klein, J Dippon, R Kerb, ...
Journal of clinical oncology 26 (13), 2131-2138, 2008
4862008
NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity
T Moriyama, R Nishii, V Perez-Andreu, W Yang, FA Klussmann, X Zhao, ...
Nature genetics 48 (4), 367-373, 2016
4832016
Treatment of chronic hepatitis D with the entry inhibitor myrcludex B: First results of a phase Ib/IIa study
P Bogomolov, A Alexandrov, N Voronkova, M Macievich, K Kokina, ...
Journal of hepatology 65 (3), 490-498, 2016
4612016
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