274 related articles for article (PubMed ID: 28164237)
21. Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion.
Pradella LM; Zuntini R; Magini P; Ceccarelli C; Neri I; Cerasoli S; Graziano C; Gasparre G; Turchetti D
J Med Genet; 2011 Nov; 48(11):779-82. PubMed ID: 21926107
[TBL] [Abstract][Full Text] [Related]
22. Cowden syndrome.
Gustafson S; Zbuk KM; Scacheri C; Eng C
Semin Oncol; 2007 Oct; 34(5):428-34. PubMed ID: 17920899
[TBL] [Abstract][Full Text] [Related]
23. Cowden syndrome-affected patients with PTEN promoter mutations demonstrate abnormal protein translation.
Teresi RE; Zbuk KM; Pezzolesi MG; Waite KA; Eng C
Am J Hum Genet; 2007 Oct; 81(4):756-67. PubMed ID: 17847000
[TBL] [Abstract][Full Text] [Related]
24. PTEN hamartoma tumor syndrome: clinical risk assessment and management protocol.
Ngeow J; Eng C
Methods; 2015 May; 77-78():11-9. PubMed ID: 25461771
[TBL] [Abstract][Full Text] [Related]
25. Thyroid Follicular Cell-derived Carcinomas in a Background of Multiple Adenomatous Nodules Leading to a Diagnosis of
Liu A; Borges PM; Tay YS; Thompson LDR; Kong MX; Lai J
Anticancer Res; 2022 Mar; 42(3):1481-1485. PubMed ID: 35220242
[TBL] [Abstract][Full Text] [Related]
26. Distinct Alterations in Tricarboxylic Acid Cycle Metabolites Associate with Cancer and Autism Phenotypes in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome.
Yehia L; Ni Y; Feng F; Seyfi M; Sadler T; Frazier TW; Eng C
Am J Hum Genet; 2019 Oct; 105(4):813-821. PubMed ID: 31564436
[TBL] [Abstract][Full Text] [Related]
27. Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma.
Zbuk KM; Patocs A; Shealy A; Sylvester H; Miesfeldt S; Eng C
Nat Clin Pract Oncol; 2007 Oct; 4(10):608-12. PubMed ID: 17898811
[TBL] [Abstract][Full Text] [Related]
28. Differential expression of novel naturally occurring splice variants of PTEN and their functional consequences in Cowden syndrome and sporadic breast cancer.
Agrawal S; Eng C
Hum Mol Genet; 2006 Mar; 15(5):777-87. PubMed ID: 16436456
[TBL] [Abstract][Full Text] [Related]
29. Novel Germline
Lopez C; Abuel-Haija M; Pena L; Coppola D
Cancer Genomics Proteomics; 2018; 15(2):115-120. PubMed ID: 29496690
[TBL] [Abstract][Full Text] [Related]
30. Pten loss in the mouse thyroid causes goiter and follicular adenomas: insights into thyroid function and Cowden disease pathogenesis.
Yeager N; Klein-Szanto A; Kimura S; Di Cristofano A
Cancer Res; 2007 Feb; 67(3):959-66. PubMed ID: 17283127
[TBL] [Abstract][Full Text] [Related]
31. Inhibition of PTEN Ameliorates Secondary Hippocampal Injury and Cognitive Deficits after Intracerebral Hemorrhage: Involvement of AKT/FoxO3a/ATG-Mediated Autophagy.
Zhao M; Gao J; Cui C; Zhang Y; Jiang X; Cui J
Oxid Med Cell Longev; 2021; 2021():5472605. PubMed ID: 33777313
[TBL] [Abstract][Full Text] [Related]
32. KLLN epigenotype-phenotype associations in Cowden syndrome.
Nizialek EA; Mester JL; Dhiman VK; Smiraglia DJ; Eng C
Eur J Hum Genet; 2015 Nov; 23(11):1538-43. PubMed ID: 25669429
[TBL] [Abstract][Full Text] [Related]
33. PTEN: one gene, many syndromes.
Eng C
Hum Mutat; 2003 Sep; 22(3):183-98. PubMed ID: 12938083
[TBL] [Abstract][Full Text] [Related]
34. Neuroendocrine Tumor of the Pancreas as a Manifestation of Cowden Syndrome: A Case Report.
Neychev V; Sadowski SM; Zhu J; Allgaeuer M; Kilian K; Meltzer P; Kebebew E
J Clin Endocrinol Metab; 2016 Feb; 101(2):353-8. PubMed ID: 26678657
[TBL] [Abstract][Full Text] [Related]
35. Germline PIK3CA and AKT1 mutations in Cowden and Cowden-like syndromes.
Orloff MS; He X; Peterson C; Chen F; Chen JL; Mester JL; Eng C
Am J Hum Genet; 2013 Jan; 92(1):76-80. PubMed ID: 23246288
[TBL] [Abstract][Full Text] [Related]
36. Germline PTEN Mutation Analysis for PTEN Hamartoma Tumor Syndrome.
Ngeow J; Eng C
Methods Mol Biol; 2016; 1388():63-73. PubMed ID: 27033071
[TBL] [Abstract][Full Text] [Related]
37. No mutations but an increased frequency of SDHx polymorphisms in patients with sporadic and familial medullary thyroid carcinoma.
Montani M; Schmitt AM; Schmid S; Locher T; Saremaslani P; Heitz PU; Komminoth P; Perren A
Endocr Relat Cancer; 2005 Dec; 12(4):1011-6. PubMed ID: 16322339
[TBL] [Abstract][Full Text] [Related]
38. PTEN in colorectal cancer: a report on two Cowden syndrome patients.
Kersseboom R; Dubbink HJ; Corver WE; van Tilburg AJ; Poley JW; van Leerdam ME; Atmodimedjo PN; van de Laar IM; Collée JM; Dinjens WN; Morreau H; Wagner A
Clin Genet; 2012 Jun; 81(6):555-62. PubMed ID: 21291452
[TBL] [Abstract][Full Text] [Related]
39. Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
Chen HJ; Romigh T; Sesock K; Eng C
Hum Mutat; 2017 Oct; 38(10):1372-1377. PubMed ID: 28677221
[TBL] [Abstract][Full Text] [Related]
40. Comparative genomic and functional analyses reveal a novel cis-acting PTEN regulatory element as a highly conserved functional E-box motif deleted in Cowden syndrome.
Pezzolesi MG; Zbuk KM; Waite KA; Eng C
Hum Mol Genet; 2007 May; 16(9):1058-71. PubMed ID: 17341483
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
