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Role of PTEN, a Lipid Phosphatase Upstream Effector of Protein Kinase B, in Epithelial Thyroid Carcinogenesis.
- Published in:
- Annals of the New York Academy of Sciences, 2002, v. 968, n. 1, p. 213, doi. 10.1111/j.1749-6632.2002.tb04337.x
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- Publication type:
- Article
Germline and somatic DNA methylation and epigenetic regulation of KILLIN in renal cell carcinoma.
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- Genes, Chromosomes & Cancer, 2011, v. 50, n. 8, p. 654, doi. 10.1002/gcc.20887
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- Publication type:
- Article
HPV status-independent association of alcohol and tobacco exposure or prior radiation therapy with promoter methylation of FUSSEL18, EBF3, IRX1, and SEPT9, but not SLC5A8, in head and neck squamous cell carcinomas.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 4, p. 319, doi. 10.1002/gcc.20742
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- Publication type:
- Article
Opposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma cases.
- Published in:
- Human Genetics, 2001, v. 109, n. 2, p. 146, doi. 10.1007/s004390100563
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- Publication type:
- Article
Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease.
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- Human Genetics, 2001, v. 108, n. 5, p. 409, doi. 10.1007/s004390100506
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- Publication type:
- Article
Constitutional mislocalization of Pten drives precocious maturation in oligodendrocytes and aberrant myelination in model of autism spectrum disorder.
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- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0364-7
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- Publication type:
- Article
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours.
- Published in:
- Oncogene, 2001, v. 20, n. 51, p. 7573, doi. 10.1038/sj.onc.1204968
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- Publication type:
- Article
Over-representation of a germline variant in the gene encoding RET co-receptor GFRα-1 but not GFRα-2 or GFRα-3 in cases with sporadic medullary thyroid carcinoma.
- Published in:
- Oncogene, 2001, v. 20, n. 17, p. 2161, doi. 10.1038/sj.onc.1204289
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- Publication type:
- Article
Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours.
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- Oncogene, 2000, v. 19, n. 16, p. 2060, doi. 10.1038/sj.onc.1203537
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- Publication type:
- Article
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation.
- Published in:
- Oncogene, 1999, v. 18, n. 6, p. 1369, doi. 10.1038/sj.onc.1202418
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- Publication type:
- Article
Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer.
- Published in:
- Oncogene, 1998, v. 17, n. 6, p. 727, doi. 10.1038/sj.onc.1201984
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- Publication type:
- Article
PTEN/MMAC1/TEP1 involvement in primary prostate cancers.
- Published in:
- Oncogene, 1998, v. 16, n. 22, p. 2879, doi. 10.1038/sj.onc.1202081
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- Publication type:
- Article
A highly conserved processed PTEN pseudogene is located on chromosome band 9p21.
- Published in:
- Oncogene, 1998, v. 16, n. 18, p. 2403, doi. 10.1038/sj.onc.1201762
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- Publication type:
- Article
PTEN mutations in gliomas and glioneuronal tumors.
- Published in:
- Oncogene, 1998, v. 16, n. 17, p. 2259, doi. 10.1038/sj.onc.1201756
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- Publication type:
- Article
Analysis of PTEN and the 10q23 region in primary prostate carcinomas.
- Published in:
- Oncogene, 1998, v. 16, n. 13, p. 1743, doi. 10.1038/sj.onc.1200205
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- Publication type:
- Article
Genomic structure and chromosomal localization of the human GDNFR-α gene.
- Published in:
- Oncogene, 1998, v. 16, n. 5, p. 597, doi. 10.1038/sj.onc.1201573
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- Publication type:
- Article
Increased PTEN expression due to transcriptional activation of PPARγ by Lovastatin and Rosiglitazone.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 10, p. 2390, doi. 10.1002/ijc.21799
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- Publication type:
- Article
Coffee consumption and breast cancer risk among BRCA1 and BRCA2 mutation carriers.
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- International Journal of Cancer, 2006, v. 118, n. 1, p. 103, doi. 10.1002/ijc.21296
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- Publication type:
- Article
Nuclear PTEN expression and clinicopathologic features in a population-based series of primary cutaneous melanoma.
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- International Journal of Cancer, 2002, v. 99, n. 1, p. 63, doi. 10.1002/ijc.10294
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- Publication type:
- Article
Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain.
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- International Journal of Cancer, 2002, v. 98, n. 5, p. 774, doi. 10.1002/ijc.10240
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- Publication type:
- Article
Mutation analysis of NTRK2 and NTRK3, encoding 2 tyrosine kinase receptors, in sporadic human medullary thyroid carcinoma reveals novel sequence variants.
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- International Journal of Cancer, 2001, v. 92, n. 1, p. 70, doi. 10.1002/1097-0215(200102)9999:9999<::AID-IJC1153>3.0.CO;2-N
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- Publication type:
- Article
No evidence for germline PTEN mutations in families with breast and brain tumours.
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- International Journal of Cancer, 1999, v. 84, n. 3, p. 216, doi. 10.1002/(SICI)1097-0215(19990621)84:3<216::AID-IJC3>3.0.CO;2-E
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- Publication type:
- Article
Germline nuclear-predominant Pten murine model exhibits impaired social and perseverative behavior, microglial activation, and increased oxytocinergic activity.
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- Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00448-4
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- Publication type:
- Article
Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autism.
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- Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-020-00406-6
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- Publication type:
- Article
Decreased nuclear Pten in neural stem cells contributes to deficits in neuronal maturation.
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- Molecular Autism, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13229-020-00337-2
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- Publication type:
- Article
Non-canonical role of wild-type SEC23B in the cellular stress response pathway.
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- Cell Death & Disease, 2021, v. 12, n. 4, p. 1, doi. 10.1038/s41419-021-03589-9
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- Publication type:
- Article
WWP1 germline variants are associated with normocephalic autism spectrum disorder.
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- Cell Death & Disease, 2020, v. 11, n. 7, p. 1, doi. 10.1038/s41419-020-2681-z
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- Publication type:
- Article
Pulmonary arterial hypertension in a patient with Cowden syndrome and the PTEN mutation.
- Published in:
- 2014
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- Publication type:
- Case Study
Germline Genomic Homozygosity and Cancer Risk.
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- 2008
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- Publication type:
- Letter
Frequency of germline genomic homozygosity associated with cancer cases.
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- 2008
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- Publication type:
- journal article
Frequency of Germline Genomic Homozygosity Associated With Cancer Cases.
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- JAMA: Journal of the American Medical Association, 2008, v. 299, n. 12, p. 1437
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- Publication type:
- Article
Genomic Instability Within Tumor Stroma and Clinicopathological Characteristics of Sporadic Primary Invasive Breast Carcinoma.
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- JAMA: Journal of the American Medical Association, 2007, v. 297, n. 19, p. 2103, doi. 10.1001/jama.297.19.2103
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- Publication type:
- Article
Microenvironmental Genomic Alterations and Clinicopathological Behavior in Head and Neck Squamous Cell Carcinoma.
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- JAMA: Journal of the American Medical Association, 2007, v. 297, n. 2, p. 187, doi. 10.1001/jama.297.2.187
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- Publication type:
- Article
Salpingo-oophorectomy and the Risk of Ovarian, Fallopian Tube, and Peritoneal Cancers in Women With a BRCA1 or BRCA2 Mutation.
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- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 2, p. 185, doi. 10.1001/jama.296.2.185
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- Publication type:
- Article
Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis.
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- JAMA: Journal of the American Medical Association, 2005, v. 294, n. 19, p. 2465, doi. 10.1001/jama.294.19.2465
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- Publication type:
- Article
Distinct Clinical Features of Paraganglioma Syndromes Associated With SDHB and SDHD Gene Mutations.
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- JAMA: Journal of the American Medical Association, 2004, v. 292, n. 8, p. 943, doi. 10.1001/jama.292.8.943
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- Publication type:
- Article
Decision aids from genetics to treatment of breast cancer: long-term clinical utility or temporary solution?
- Published in:
- 2004
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- Publication type:
- commentary
The association between the myelodysplastic syndromes and Crohn disease.
- Published in:
- 1992
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- Publication type:
- journal article
Shape shifting: The multiple conformational substates of the PTEN N‐terminal PIP<sub>2</sub>‐binding domain.
- Published in:
- Protein Science: A Publication of the Protein Society, 2022, v. 31, n. 5, p. 1, doi. 10.1002/pro.4308
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- Publication type:
- Article
Structure‐based Computational Modeling of Germline PTEN Mutations in Cancer and Autism Risk: Implications for Therapeutic Targeting.
- Published in:
- FASEB Journal, 2022, v. 36, p. N.PAG, doi. 10.1096/fasebj.2022.36.S1.R2719
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- Publication type:
- Article
Genetics and genomics in healthcare: the future is now.
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- Singapore Medical Journal, 2023, v. 64, n. 1, p. 4, doi. 10.4103/SINGAPOREMEDJ.SMJ-2021-346
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- Publication type:
- Article
Should providers warn others of genetic results?
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- Medical Ethics Advisor, 2012, v. 28, n. 7, p. 79
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- Publication type:
- Article
Mendelian genetics of rare-and not so rare-cancers.
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- Annals of the New York Academy of Sciences, 2010, v. 1214, n. 1, p. 70, doi. 10.1111/j.1749-6632.2010.05789.x
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- Publication type:
- Article
Genetic and Clinical Investigation of Pheochromocytoma.
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- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 122, doi. 10.1196/annals.1353.013
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- Publication type:
- Article
FROM DEVELOPMENTAL DISORDER TO HERITABLE CANCER: IT'S ALL IN THE BMP/TGF-β FAMILY.
- Published in:
- Nature Reviews Genetics, 2003, v. 4, n. 10, p. 763, doi. 10.1038/nrg1178
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- Publication type:
- Article
Maternal genetics influences fetal neurodevelopment and postnatal autism spectrum disorder-like phenotype by modulating in-utero immunosuppression.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01472-x
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- Publication type:
- Article
184. The microbiome of temporal arteries.
- Published in:
- 2019
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- Publication type:
- Abstract
183. Microbiome in aortitis.
- Published in:
- 2019
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- Publication type:
- Abstract
Cowden syndrome-associated germline SDHD variants alter PTEN nuclear translocation through SRC-induced PTEN oxidation
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 1, p. 142, doi. 10.1093/hmg/ddu425
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- Publication type:
- Article
Germline disruption of Pten localization causes enhanced sex-dependent social motivation and increased glial production.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 12, p. 3212, doi. 10.1093/hmg/ddu031
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- Publication type:
- Article