Lista de obras - L Inglada-Pérez - Dominio Público Uruguay

Allelic variant at -79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels.

artículo científico publicado en 2010

An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.

artículo científico publicado en 2013

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore

artículo científico publicado en 2015

Correction: An Epistatic Interaction between the PAX8 and STK17B Genes in Papillary Thyroid Cancer Susceptibility

artículo científico publicado en 2013

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

artículo científico publicado en 2015

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

artículo científico publicado en 2015

DNA methylation profiling of well-differentiated thyroid cancer uncovers markers of recurrence free survival.

artículo científico publicado en 2014

Deep sequencing reveals microRNAs predictive of antiangiogenic drug response

artículo científico publicado en 2016

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

artículo científico publicado en 2011

Functional and in silico assessment of MAX variants of unknown significance

artículo científico publicado en 2015

Genetic anticipation is associated with telomere shortening in hereditary breast cancer.

artículo científico publicado en 2011

Genetic variation in the SLC19A1 gene and methotrexate toxicity in rheumatoid arthritis patients.

artículo científico publicado en 2012

Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy

scientific journal article

Hematologic β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicity.

artículo científico publicado en 2012

High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme

Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

artículo científico publicado en 2014

Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways

artículo científico publicado en 2013

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

scientific article published on 27 March 2012

MicroRNA deep-sequencing reveals master regulators of follicular and papillary thyroid tumors.

artículo científico publicado en 2015

Molecular insights into the OGG1 gene, a cancer risk modifier in BRCA1 and BRCA2 mutations carriers

scientific article published on 22 March 2016

Multilayer OMIC Data in Medullary Thyroid Carcinoma Identifies the STAT3 Pathway as a Potential Therapeutic Target in RETM918T Tumors.

artículo científico publicado en 2016

Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis.

artículo científico publicado en 2010

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

artículo científico publicado en 2015

Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy.

artículo científico publicado en 2012

Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas

artículo científico publicado en 2010

SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency.

artículo científico publicado en 2012

Short telomeres are frequent in hereditary breast tumors and are associated with high tumor grade

artículo científico publicado en 2013

Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases.

artículo científico publicado en 2012

Targeted Sequencing Reveals Low-Frequency Variants in EPHA Genes as Markers of Paclitaxel-Induced Peripheral Neuropathy.

artículo científico publicado en 2016

The miR-200 family controls -tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients

artículo científico publicado en 2010

The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors

artículo científico publicado en 2009

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations

artículo científico publicado en 2015

Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection.

artículo científico publicado en 2015

Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis

artículo científico publicado en 2013

VEGF, VEGFR3, and PDGFRB protein expression is influenced by RAS mutations in medullary thyroid carcinoma.

artículo científico publicado en 2014

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.

artículo científico publicado en 2015

Lista de obras de L Inglada-Pérez

Allelic variant at -79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels.

An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore

Correction: An Epistatic Interaction between the PAX8 and STK17B Genes in Papillary Thyroid Cancer Susceptibility

DNA Methylation Profiling in Pheochromocytoma and Paraganglioma Reveals Diagnostic and Prognostic Markers

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

DNA methylation profiling of well-differentiated thyroid cancer uncovers markers of recurrence free survival.

Deep sequencing reveals microRNAs predictive of antiangiogenic drug response

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Functional and in silico assessment of MAX variants of unknown significance

Genetic anticipation is associated with telomere shortening in hereditary breast cancer.

Genetic variation in the SLC19A1 gene and methotrexate toxicity in rheumatoid arthritis patients.

Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy

Hematologic β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicity.

High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme

Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

MicroRNA deep-sequencing reveals master regulators of follicular and papillary thyroid tumors.

Molecular insights into the OGG1 gene, a cancer risk modifier in BRCA1 and BRCA2 mutations carriers

Multilayer OMIC Data in Medullary Thyroid Carcinoma Identifies the STAT3 Pathway as a Potential Therapeutic Target in RETM918T Tumors.

Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis.

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy.

Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas

SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency.

Short telomeres are frequent in hereditary breast tumors and are associated with high tumor grade

Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases.

Targeted Sequencing Reveals Low-Frequency Variants in EPHA Genes as Markers of Paclitaxel-Induced Peripheral Neuropathy.

The miR-200 family controls -tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients

The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations

Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection.

Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis

VEGF, VEGFR3, and PDGFRB protein expression is influenced by RAS mutations in medullary thyroid carcinoma.

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.