187 related articles for article (PubMed ID: 28513612)
1. Insertion of Alu elements at a PTEN hotspot in Cowden syndrome.
Crivelli L; Bubien V; Jones N; Chiron J; Bonnet F; Barouk-Simonet E; Couzigou P; Sevenet N; Caux F; Longy M
Eur J Hum Genet; 2017 Sep; 25(9):1087-1091. PubMed ID: 28513612
[TBL] [Abstract][Full Text] [Related]
2. Ovarian Clear Cell Carcinoma in Cowden Syndrome.
Yauy K; Imbert-Bouteille M; Bubien V; Lindet-Bourgeois C; Rathat G; Perrochia H; MacGrogan G; Longy M; Bessis D; Tinat J; Baert-Desurmont S; Blanluet M; Perre PV; Baudry K; Pujol P; Corsini C
J Natl Compr Canc Netw; 2019 Jan; 17(1):7-11. PubMed ID: 30659124
[TBL] [Abstract][Full Text] [Related]
3. Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes.
Ni Y; Zbuk KM; Sadler T; Patocs A; Lobo G; Edelman E; Platzer P; Orloff MS; Waite KA; Eng C
Am J Hum Genet; 2008 Aug; 83(2):261-8. PubMed ID: 18678321
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A case of Cowden syndrome with a novel mutation in the PTEN gene.
Kawase Y; Matsudate Y; Kubo Y
J Med Invest; 2020; 67(1.2):200-201. PubMed ID: 32378608
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel mutation of the PTEN gene in a Japanese patient with Cowden syndrome and bilateral breast cancer.
Tate G; Suzuki T; Endo Y; Mitsuya T
Cancer Genet Cytogenet; 2008 Jul; 184(1):67-71. PubMed ID: 18558293
[TBL] [Abstract][Full Text] [Related]
8. Cowden syndrome: report of two cases with immunohistochemical analysis for PTEN expression.
Zabetian S; Mehregan D
Am J Dermatopathol; 2012 Aug; 34(6):632-4. PubMed ID: 22481496
[TBL] [Abstract][Full Text] [Related]
9. Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations.
Sherman SK; Maxwell JE; Qian Q; Bellizzi AM; Braun TA; Iannettoni MD; Darbro BW; Howe JR
Cancer Genet; 2015; 208(1-2):41-6. PubMed ID: 25554686
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.
Ngeow J; Mester J; Rybicki LA; Ni Y; Milas M; Eng C
J Clin Endocrinol Metab; 2011 Dec; 96(12):E2063-71. PubMed ID: 21956414
[TBL] [Abstract][Full Text] [Related]
12. Breast cancer risk and clinical implications for germline PTEN mutation carriers.
Ngeow J; Sesock K; Eng C
Breast Cancer Res Treat; 2017 Aug; 165(1):1-8. PubMed ID: 26700035
[TBL] [Abstract][Full Text] [Related]
13. Germline SDHx variants modify breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53.
Ni Y; He X; Chen J; Moline J; Mester J; Orloff MS; Ringel MD; Eng C
Hum Mol Genet; 2012 Jan; 21(2):300-10. PubMed ID: 21979946
[TBL] [Abstract][Full Text] [Related]
14. Utility of PTEN protein dosage in predicting for underlying germline PTEN mutations among patients presenting with thyroid cancer and Cowden-like phenotypes.
Ngeow J; He X; Mester JL; Lei J; Romigh T; Orloff MS; Milas M; Eng C
J Clin Endocrinol Metab; 2012 Dec; 97(12):E2320-7. PubMed ID: 23066114
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. PTEN mosaicism with features of Cowden syndrome.
Gammon A; Jasperson K; Pilarski R; Prior T; Kuwada S
Clin Genet; 2013 Dec; 84(6):593-5. PubMed ID: 23240978
[TBL] [Abstract][Full Text] [Related]
17. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients.
Pena-Couso L; Ercibengoa M; Mercadillo F; Gómez-Sánchez D; Inglada-Pérez L; Santos M; Lanillos J; Gutiérrez-Abad D; Hernández A; Carbonell P; Letón R; Robledo M; Rodríguez-Antona C; Perea J; Urioste M;
Orphanet J Rare Dis; 2022 Feb; 17(1):85. PubMed ID: 35227301
[TBL] [Abstract][Full Text] [Related]
18. [Our experience with analysis of the PTEN gene in patients suspected of having Cowden syndrome].
Vasovcák P; Foretová L; Puchmajerová A; Senkeríková M; Martínek J; Krepelová A
Klin Onkol; 2010; 23(2):111-4. PubMed ID: 20465090
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. First report of ovarian dysgerminoma in Cowden syndrome with germline PTEN mutation and PTEN-related 10q loss of tumor heterozygosity.
Cho MY; Kim HS; Eng C; Kim DS; Kang SJ; Eom M; Yi SY; Bronner MP
Am J Surg Pathol; 2008 Aug; 32(8):1258-64. PubMed ID: 18594467
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
