Found: 25
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Tumoral and tissue-specific expression of the major human β-tubulin isotypes.
- Published in:
- Cytoskeleton, 2010, v. 67, n. 4, p. 214, doi. 10.1002/cm.20436
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- Publication type:
- Article
Identification and phenotype characterization of two CYP3A haplotypes causing different enzymatic capacity in fetal livers.
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- Clinical Pharmacology & Therapeutics, 2005, v. 77, n. 4, p. 259, doi. 10.1016/j.clpt.2004.11.003
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- Publication type:
- Article
Genetics of Pheochromocytoma and Paraganglioma in Spanish Patients.
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 5, p. 1701, doi. 10.1210/jc.2008-2756
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- Article
Genetic polymorphisms of SCN9A are associated with oxaliplatin-induced neuropathy.
- Published in:
- 2017
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- Publication type:
- journal article
Genome-wide association analyses of ovarian cancer patients undergoing primary debulking surgery identify candidate genes for residual disease.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00395-y
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- Publication type:
- Article
MicroRNAs Targeting HIF-2α, VEGFR1 and/or VEGFR2 as Potential Predictive Biomarkers for VEGFR Tyrosine Kinase and HIF-2α Inhibitors in Metastatic Clear-Cell Renal Cell Carcinoma.
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- Cancers, 2021, v. 13, n. 12, p. 3099, doi. 10.3390/cancers13123099
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- Publication type:
- Article
MicroRNAs Possibly Involved in the Development of Bone Metastasis in Clear-Cell Renal Cell Carcinoma.
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- Cancers, 2021, v. 13, n. 7, p. 1554, doi. 10.3390/cancers13071554
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- Publication type:
- Article
Novel DNMT3A Germline Variant in a Patient with Multiple Paragangliomas and Papillary Thyroid Carcinoma.
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- Cancers, 2020, v. 12, n. 11, p. 3304, doi. 10.3390/cancers12113304
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- Publication type:
- Article
Improving pharmacovigilance in Europe: TPMT genotyping and phenotyping in the UK and Spain.
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- European Journal of Human Genetics, 2009, v. 17, n. 8, p. 991, doi. 10.1038/ejhg.2009.10
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- Publication type:
- Article
Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients.
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- 2022
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- Publication type:
- journal article
PharmVar GeneFocus: CYP4F2.
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- Clinical Pharmacology & Therapeutics, 2024, v. 116, n. 4, p. 963, doi. 10.1002/cpt.3405
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- Publication type:
- Article
Association of single nucleotide polymorphisms in IL8 and IL13 with sunitinib-induced toxicity in patients with metastatic renal cell carcinoma.
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- European Journal of Clinical Pharmacology, 2015, v. 71, n. 12, p. 1477, doi. 10.1007/s00228-015-1935-7
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- Publication type:
- Article
Human genetics: international projects and personalized medicine.
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- Drug Metabolism & Personalized Therapy, 2016, v. 31, n. 1, p. 3, doi. 10.1515/dmpt-2015-0032
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- Publication type:
- Article
Progress in pharmacogenetics: consortiums and new strategies.
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- Drug Metabolism & Personalized Therapy, 2016, v. 31, n. 1, p. 17, doi. 10.1515/dmpt-2015-0039
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- Publication type:
- Article
Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis.
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- Human Molecular Genetics, 2013, v. 22, n. 11, p. 2169, doi. 10.1093/hmg/ddt069
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- Publication type:
- Article
Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family.
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- Genes, Chromosomes & Cancer, 2011, v. 50, n. 11, p. 922, doi. 10.1002/gcc.20911
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- Publication type:
- Article
Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: A possible hot spot?
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 3, p. 213
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- Publication type:
- Article
Effect of the Most Relevant CYP3A4 and CYP3A5 Polymorphisms on the Pharmacokinetic Parameters of 10 CYP3A Substrates.
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- Biomedicines, 2020, v. 8, n. 4, p. 94, doi. 10.3390/biomedicines8040094
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- Publication type:
- Article
VEGF, VEGFR3, and PDGFRB Protein Expression Is Influenced by RAS Mutations in Medullary Thyroid Carcinoma.
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- Thyroid, 2014, v. 24, n. 8, p. 1251, doi. 10.1089/thy.2013.0579
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- Publication type:
- Article
Loss of the actin regulator HSPC300 results in clear cell renal cell carcinoma protection in Von Hippel-Lindau patients.
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- Human Mutation, 2007, v. 28, n. 6, p. 613, doi. 10.1002/humu.20496
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- Publication type:
- Article
Functional and in silico assessment of MAX variants of unknown significance.
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- Journal of Molecular Medicine, 2015, v. 93, n. 11, p. 1247, doi. 10.1007/s00109-015-1306-y
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- Publication type:
- Article
Concomitant Medications and Risk of Chemotherapy‐Induced Peripheral Neuropathy.
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- Oncologist, 2019, v. 24, n. 8, p. e784, doi. 10.1634/theoncologist.2018-0418
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- Publication type:
- Article
A nicotine C-oxidase gene (CYP2A6) polymorphism important for promoter activity (Communicated by Bruce Gottlieb).
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- Human Mutation, 2004, v. 23, n. 3, p. 258, doi. 10.1002/humu.20002
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- Publication type:
- Article
SDHC mutation in an elderly patient without familial antecedents.
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- Clinical Endocrinology, 2008, v. 69, n. 6, p. 906, doi. 10.1111/j.1365-2265.2008.03368.x
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- Publication type:
- Article
Polymorphisms associated with everolimus pharmacokinetics, toxicity and survival in metastatic breast cancer.
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- PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0180192
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- Publication type:
- Article