Found: 107
Select item for more details and to access through your institution.
Transcriptome analysis discloses dysregulated genes in normal appearing tumor-adjacent thyroid tissues from patients with papillary thyroid carcinoma.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-93526-9
- By:
- Publication type:
- Article
Adiposity, metabolites, and colorectal cancer risk: Mendelian randomization study.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Characterizing the function of EPB41L4A in the predisposition to papillary thyroid carcinoma.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-76606-0
- By:
- Publication type:
- Article
Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in APC, BRAF, and KTM2D.
- Published in:
- Thyroid, 2020, v. 30, n. 3, p. 380, doi. 10.1089/thy.2019.0561
- By:
- Publication type:
- Article
A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres.
- Published in:
- Thyroid, 2020, v. 30, n. 2, p. 204, doi. 10.1089/thy.2019.0156
- By:
- Publication type:
- Article
Clinical implications of GWAS variants associated with differentiated thyroid cancer.
- Published in:
- Polish Journal of Endocrinology / Endokrynologia Polska, 2019, v. 70, n. 5, p. 423, doi. 10.5603/EP.a2019.0027
- By:
- Publication type:
- Article
Identification of Rare Variants Predisposing to Thyroid Cancer.
- Published in:
- Thyroid, 2019, v. 29, n. 7, p. 946, doi. 10.1089/thy.2018.0736
- By:
- Publication type:
- Article
Microsatellite Instability Occurs in a Subset of Follicular Thyroid Cancers.
- Published in:
- Thyroid, 2019, v. 29, n. 4, p. 523, doi. 10.1089/thy.2018.0655
- By:
- Publication type:
- Article
Risk Haplotypes Uniquely Associated with Radioiodine-Refractory Thyroid Cancer Patients of High African Ancestry.
- Published in:
- Thyroid, 2019, v. 29, n. 4, p. 530, doi. 10.1089/thy.2018.0687
- By:
- Publication type:
- Article
Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 431, doi. 10.1007/s10689-017-0048-0
- By:
- Publication type:
- Article
Identification of a Recurrent <italic>LMO7–BRAF</italic> Fusion in Papillary Thyroid Carcinoma.
- Published in:
- Thyroid, 2018, v. 28, n. 6, p. 748, doi. 10.1089/thy.2017.0258
- By:
- Publication type:
- Article
The Role of NRG1 in the Predisposition to Papillary Thyroid Carcinoma.
- Published in:
- 2017
- By:
- Publication type:
- journal article
The Olympic Games and Athletic Sex Assignment.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Papillary Thyroid Carcinoma: Association Between Germline DNA Variant Markers and Clinical Parameters.
- Published in:
- Thyroid, 2016, v. 26, n. 9, p. 1276, doi. 10.1089/thy.2015.0665
- By:
- Publication type:
- Article
Primary Cell Culture Systems for Human Thyroid Studies.
- Published in:
- Thyroid, 2016, v. 26, n. 8, p. 1131, doi. 10.1089/thy.2015.0518
- By:
- Publication type:
- Article
Genome-Wide Expression Screening Discloses Long Noncoding RNAs Involved in Thyroid Carcinogenesis.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Structural characterization of NRAS isoform 5.
- Published in:
- Protein Science: A Publication of the Protein Society, 2016, v. 25, n. 5, p. 1069, doi. 10.1002/pro.2916
- By:
- Publication type:
- Article
HABP2 G534E Variant in Papillary Thyroid Carcinoma.
- Published in:
- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0146315
- By:
- Publication type:
- Article
PTCSC3 Is Involved in Papillary Thyroid Carcinoma Development by Modulating S100A4 Gene Expression.
- Published in:
- 2015
- By:
- Publication type:
- journal article
A germline mutation in SRRM2, a splicing factor gene, is implicated in papillary thyroid carcinoma predisposition.
- Published in:
- Scientific Reports, 2015, p. 10566, doi. 10.1038/srep10566
- By:
- Publication type:
- Article
Biallelic MUTYH mutations can mimic Lynch syndrome.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 11, p. 1334, doi. 10.1038/ejhg.2014.15
- By:
- Publication type:
- Article
Intronic miR-3151 Within BAALC Drives Leukemogenesis by Deregulating the TP53 Pathway.
- Published in:
- Science Signaling, 2014, v. 7, n. 321, p. 1, doi. 10.1126/scisignal.2004762
- By:
- Publication type:
- Article
Cumulative Risk Impact of Five Genetic Variants Associated with Papillary Thyroid Carcinoma.
- Published in:
- Thyroid, 2013, v. 23, n. 12, p. 1532, doi. 10.1089/thy.2013.0102
- By:
- Publication type:
- Article
Unraveling the genetic predisposition to differentiated thyroid carcinoma.
- Published in:
- 2013
- By:
- Publication type:
- editorial
Characterization of a New Chronic Lymphocytic Leukemia Cell Line for Mechanistic <i>In Vitro</i> and <i>In Vivo</i> Studies Relevant to Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0076607
- By:
- Publication type:
- Article
In-depth characterization of the microRNA transcriptome in normal thyroid and papillary thyroid carcinoma.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Germline Allele-Specific Expression of DAPK1 in Chronic Lymphocytic Leukemia.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055261
- By:
- Publication type:
- Article
Identification of Lynch Syndrome Among Patients With Colorectal Cancer.
- Published in:
- JAMA: Journal of the American Medical Association, 2012, v. 308, n. 15, p. 1555, doi. 10.1001/jama.2012.13088
- By:
- Publication type:
- Article
Cancer Risks for Relatives of Patients With Serrated Polyposis.
- Published in:
- American Journal of Gastroenterology (Springer Nature), 2012, v. 107, n. 5, p. 770, doi. 10.1038/ajg.2012.52
- By:
- Publication type:
- Article
An American founder mutation in MLH1.
- Published in:
- International Journal of Cancer, 2012, v. 130, n. 9, p. 2088, doi. 10.1002/ijc.26233
- By:
- Publication type:
- Article
Evaluation of Allele-Specific Somatic Changes of Genome-Wide Association Study Susceptibility Alleles in Human Colorectal Cancers.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037672
- By:
- Publication type:
- Article
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
- Published in:
- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 56, doi. 10.1186/1750-1172-7-56
- By:
- Publication type:
- Article
MicroRNA Signature in Thyroid Fine Needle Aspiration Cytology Applied to 'Atypia of Undetermined Significance' Cases.
- Published in:
- Thyroid, 2012, v. 22, n. 1, p. 9, doi. 10.1089/thy.2011.0081
- By:
- Publication type:
- Article
MicroRNAs in Thyroid Cancer.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 11, p. 3326, doi. 10.1210/jc.2011-1004
- By:
- Publication type:
- Article
Telomere length and telomerase reverse transcriptase gene copy number in patients with papillary thyroid carcinoma.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Thyroid hormone receptor beta (THRB) is a major target gene for microRNAs deregulated in papillary thyroid carcinoma (PTC).
- Published in:
- 2011
- By:
- Publication type:
- journal article
Allele-specific expression of TGFBR1 in colon cancer patients.
- Published in:
- Carcinogenesis, 2010, v. 31, n. 10, p. 1800, doi. 10.1093/carcin/bgq165
- By:
- Publication type:
- Article
Low cancer incidence rates in Ohio Amish.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Identifying Lynch syndrome.
- Published in:
- International Journal of Cancer, 2009, v. 125, n. 6, p. 1492, doi. 10.1002/ijc.24491
- By:
- Publication type:
- Article
Lynch syndrome deletions in unexpected places.
- Published in:
- Human Mutation, 2009, v. 30, n. 2, p. v, doi. 10.1002/humu.20984
- By:
- Publication type:
- Article
The Frequency of Muir-Torre Syndrome Among Lynch Syndrome Families.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 4, p. 277, doi. 10.1093/jnci/djm291
- By:
- Publication type:
- Article
Molecular profiling of chronic lymphocytic leukaemia: genetics meets epigenetics to identify predisposing genes.
- Published in:
- British Journal of Haematology, 2007, v. 139, n. 5, p. 744, doi. 10.1111/j.1365-2141.2007.06875.x
- By:
- Publication type:
- Article
Identification of a novel noncoding RNA gene, NAMA, that is downregulated in papillary thyroid carcinoma with BRAF mutation and associated with growth arrest.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 4, p. 767, doi. 10.1002/ijc.22701
- By:
- Publication type:
- Article
Evidence for heritable predisposition to epigenetic silencing of MLH1.
- Published in:
- International Journal of Cancer, 2007, v. 120, n. 8, p. 1684, doi. 10.1002/ijc.22406
- By:
- Publication type:
- Article
Response to: getting rid of the PMS2 pseudogenes: mission impossible?
- Published in:
- Human Mutation, 2007, v. 28, n. 4, p. 415, doi. 10.1002/humu.20446
- By:
- Publication type:
- Article
Long-range PCR facilitates the identification of PMS2-specific mutations.
- Published in:
- Human Mutation, 2006, v. 27, n. 11, p. 1155, doi. 10.1002/humu.20437
- By:
- Publication type:
- Article
Long-range PCR facilitates the identification of PMS2-specific mutations.
- Published in:
- Human Mutation, 2006, v. 27, n. 5, p. 490, doi. 10.1002/humu.20318
- By:
- Publication type:
- Article
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 390, doi. 10.1038/sj.ejhg.5201584
- By:
- Publication type:
- Article
American founder mutation for Lynch syndrome: Prevalence estimates and implications.
- Published in:
- Cancer (0008543X), 2006, v. 106, n. 2, p. 448
- By:
- Publication type:
- Article
The Incidence of Lynch Syndrome.
- Published in:
- Familial Cancer, 2005, v. 4, n. 3, p. 233
- By:
- Publication type:
- Article