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Association Between ABCB1 Genetic Variants and Persistent Chemotherapy-Induced Alopecia in Women With Breast Cancer.
- Published in:
- 2020
- By:
- Publication type:
- journal article
A Comprehensive Analysis of 21 Actionable Pharmacogenes in the Spanish Population: From Genetic Characterisation to Clinical Impact.
- Published in:
- Pharmaceutics, 2023, v. 15, n. 4, p. 1286, doi. 10.3390/pharmaceutics15041286
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- Publication type:
- Article
POLRMT as a Novel Susceptibility Gene for Cardiotoxicity in Epirubicin Treatment of Breast Cancer Patients.
- Published in:
- Pharmaceutics, 2021, v. 13, n. 11, p. 1942, doi. 10.3390/pharmaceutics13111942
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- Publication type:
- Article
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss.
- Published in:
- EMBO Molecular Medicine, 2016, v. 8, n. 11, p. 1289, doi. 10.15252/emmm.201505815
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- Publication type:
- Article
Gene amplification of the transcription factor DP1 and CTNND1 in human lung cancer.
- Published in:
- Journal of Pathology, 2010, v. 222, n. 1, p. 89, doi. 10.1002/path.2732
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- Publication type:
- Article
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma.
- Published in:
- Nature Genetics, 2011, v. 43, n. 7, p. 663, doi. 10.1038/ng.861
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- Publication type:
- Article
Genetic analysis of three important genes in pigmentation and melanoma susceptibility: CDKN2A, MC1R and HERC2/OCA2.
- Published in:
- Experimental Dermatology, 2010, v. 19, n. 9, p. 836, doi. 10.1111/j.1600-0625.2010.01115.x
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- Publication type:
- Article
Pigmentation-related genes and their implication in malignant melanoma susceptibility.
- Published in:
- Experimental Dermatology, 2009, v. 18, n. 7, p. 634, doi. 10.1111/j.1600-0625.2009.00846.x
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- Publication type:
- Article
Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055681
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- Publication type:
- Article
Effect of ABCB1 and ABCC3 Polymorphisms on Osteosarcoma Survival after Chemotherapy: A Pharmacogenetic Study.
- Published in:
- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026091
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- Publication type:
- Article
A Customized Pigmentation SNP Array Identifies a Novel SNP Associated with Melanoma Predisposition in the SLC45A2 Gene.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019271
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- Publication type:
- Article
Deep Sequencing of Target Linkage Assay-Identified Regions in Familial Breast Cancer: Methods, Analysis Pipeline and Troubleshooting.
- Published in:
- PLoS ONE, 2010, v. 5, n. 4, p. 1, doi. 10.1371/journal.pone.0009976
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- Publication type:
- Article
Genetics of Pheochromocytoma and Paraganglioma in Spanish Patients.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 5, p. 1701, doi. 10.1210/jc.2008-2756
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- Publication type:
- Article
A Large Case-Control Study Performed in Spanish Population Suggests That RECQL5 Is the Only RECQ Helicase Involved in Breast Cancer Susceptibility.
- Published in:
- Cancers, 2022, v. 14, n. 19, p. 4738, doi. 10.3390/cancers14194738
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- Publication type:
- Article
Human Genomic Diversity Where the Mediterranean Joins the Atlantic.
- Published in:
- Molecular Biology & Evolution, 2020, v. 37, n. 4, p. 1041, doi. 10.1093/molbev/msz288
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- Publication type:
- Article
Exome array analysis identifies <italic>ETFB</italic> as a novel susceptibility gene for anthracycline-induced cardiotoxicity in cancer patients.
- Published in:
- Breast Cancer Research & Treatment, 2018, v. 167, n. 1, p. 249, doi. 10.1007/s10549-017-4497-9
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- Publication type:
- Article
A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 118, n. 1, p. 151, doi. 10.1007/s10549-009-0317-1
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- Publication type:
- Article
Genomic characterization of individuals presenting extreme phenotypes of high and low risk to develop tobacco‐induced lung cancer.
- Published in:
- Cancer Medicine, 2018, v. 7, n. 7, p. 3474, doi. 10.1002/cam4.1500
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- Publication type:
- Article
ParEGO extensions for multi-objective optimization of expensive evaluation functions.
- Published in:
- Journal of Global Optimization, 2017, v. 67, n. 1/2, p. 79, doi. 10.1007/s10898-016-0419-3
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- Publication type:
- Article
Diseño y plan de implementación para el montaje de una Oficina de Gestión de Proyectos (OGP) en MYV Consultores Asociados S.A.
- Published in:
- Obras y Proyectos, 2019, n. 26, p. 51, doi. 10.4067/s0718-28132019000200051
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- Publication type:
- Article
Real-world inter-observer variability of the Sequential Organ Failure Assessment (SOFA) score in intensive care medicine: the time has come for an update.
- Published in:
- 2023
- By:
- Publication type:
- Letter
Regulatory CDH4 Genetic Variants Associate With Risk to Develop Capecitabine‐Induced Hand‐Foot Syndrome.
- Published in:
- Clinical Pharmacology & Therapeutics, 2021, v. 109, n. 2, p. 462, doi. 10.1002/cpt.2013
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- Publication type:
- Article
Molecular basis of the differential interaction with lithium of glycine transporters GLYT1 and GLYT2.
- Published in:
- Journal of Neurochemistry, 2011, v. 118, n. 2, p. 195, doi. 10.1111/j.1471-4159.2011.07309.x
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- Publication type:
- Article
A crowdsourcing database for the copy-number variation of the Spanish population.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00466-8
- By:
- Publication type:
- Article
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 22, p. 6096
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- Publication type:
- Article
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 7, p. 1934, doi. 10.1093/hmg/ddt581
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- Publication type:
- Article
Hsa‐miR‐139‐5p is a prognostic thyroid cancer marker involved in HNRNPF‐mediated alternative splicing.
- Published in:
- International Journal of Cancer, 2020, v. 146, n. 2, p. 521, doi. 10.1002/ijc.32622
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- Publication type:
- Article
Whole exome sequencing identifies PLEC, EXO5 and DNAH7 as novel susceptibility genes in testicular cancer.
- Published in:
- International Journal of Cancer, 2018, v. 143, n. 8, p. 1954, doi. 10.1002/ijc.31604
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- Publication type:
- Article
Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 10, p. 2427, doi. 10.1002/ijc.29299
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- Publication type:
- Article
Real-world inter-observer variability of the Sequential Organ Failure Assessment (SOFA) score in intensive care medicine: the time has come for an update.
- Published in:
- 2023
- By:
- Publication type:
- Letter
Intermediate Molecular Phenotypes to Identify Genetic Markers of Anthracycline-Induced Cardiotoxicity Risk.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 15, p. 1956, doi. 10.3390/cells12151956
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- Publication type:
- Article
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 4, p. 1, doi. 10.1371/journal.pgen.1004256
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- Publication type:
- Article
The Variant rs1867277 in FOXE1 Gene Confers Thyroid Cancer Susceptibility through the Recruitment of USF1/ USF2 Transcription Factors.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 9, p. 1, doi. 10.1371/journal.pgen.1000637
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- Publication type:
- Article
RECQL5: Another DNA helicase potentially involved in hereditary breast cancer susceptibility.
- Published in:
- Human Mutation, 2019, v. 40, n. 5, p. 566, doi. 10.1002/humu.23732
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- Publication type:
- Article
Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.
- Published in:
- Human Mutation, 2011, v. 32, n. 2, p. 240, doi. 10.1002/humu.21398
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- Publication type:
- Article
Exome sequencing of three cases of familial exceptional longevity.
- Published in:
- Aging Cell, 2014, v. 13, n. 6, p. 1087, doi. 10.1111/acel.12261
- By:
- Publication type:
- Article
Genetic analysis of the vitamin D receptor gene in two epithelial cancers: melanoma and breast cancer case-control studies.
- Published in:
- 2008
- By:
- Publication type:
- journal article