92 related articles for article (PubMed ID: 18456716)
1. Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approach.
Chibon F; Primois C; Bressieux JM; Lacombe D; Lok C; Mauriac L; Taieb A; Longy M
J Med Genet; 2008 Oct; 45(10):657-65. PubMed ID: 18456716
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis.
van Hattem WA; Brosens LA; de Leng WW; Morsink FH; Lens S; Carvalho R; Giardiello FM; Offerhaus GJ
Gut; 2008 May; 57(5):623-7. PubMed ID: 18178612
[TBL] [Abstract][Full Text] [Related]
5. Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.
Kim DK; Myung SJ; Yang SK; Hong SS; Kim KJ; Byeon JS; Lee GH; Kim JH; Min YI; Lee SM; Jeong JY; Song K; Jung SA
Dis Colon Rectum; 2005 Sep; 48(9):1714-22. PubMed ID: 16007494
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Skin abnormalities in individuals with macrocephaly: Cowden disease from a dermatologist's point of view.
van der Velden JJ; Vreeburg M; Smeets EE; Schrander-Stumpel CT; van Steensel MA
Int J Dermatol; 2008 Nov; 47 Suppl 1():45-8. PubMed ID: 18986487
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. A novel loss-of-function mutation (N48K) in the PTEN gene in a Spanish patient with Cowden disease.
Vega A; Torres J; Torres M; Cameselle-Teijeiro J; Macia M; Carracedo A; Pulido R
J Invest Dermatol; 2003 Dec; 121(6):1356-9. PubMed ID: 14675182
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation of PTEN gene in a patient with Cowden syndrome with excessive papillomatosis of the lips, discrete cutaneous lesions, and gastrointestinal polyposis.
Vasovcak P; Krepelova A; Puchmajerova A; Spicak J; Voska L; Musilova A; Mestak J; Martinek J
Eur J Gastroenterol Hepatol; 2007 Jun; 19(6):513-7. PubMed ID: 17489063
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Cowden disease and the PTEN gene: a successfully clinical and biological combined approach].
Longy M
Bull Cancer; 2001 Dec; 88(12):1153-8. PubMed ID: 11792608
[TBL] [Abstract][Full Text] [Related]
13. How to recognize Cowden syndrome: A novel PTEN mutation description.
Delannoy P; Debray FG; Verloes A; Beckers A; Valdes-Socin H
Ann Endocrinol (Paris); 2017 Jul; 78(3):188-190. PubMed ID: 28262255
[No Abstract] [Full Text] [Related]
14. 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]
15. Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations.
Banneau G; Guedj M; MacGrogan G; de Mascarel I; Velasco V; Schiappa R; Bonadona V; David A; Dugast C; Gilbert-Dussardier B; Ingster O; Vabres P; Caux F; de Reynies A; Iggo R; Sevenet N; Bonnet F; Longy M
Breast Cancer Res; 2010; 12(4):R63. PubMed ID: 20712882
[TBL] [Abstract][Full Text] [Related]
16. Cowden syndrome: clinical case and a brief review.
Lopes S; Vide J; Moreira E; Azevedo F
Dermatol Online J; 2017 Aug; 23(8):. PubMed ID: 29469739
[TBL] [Abstract][Full Text] [Related]
17. Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome.
Orloff MS; Eng C
Oncogene; 2008 Sep; 27(41):5387-97. PubMed ID: 18794875
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Arteriovenous malformations in Cowden syndrome.
Turnbull MM; Humeniuk V; Stein B; Suthers GK
J Med Genet; 2005 Aug; 42(8):e50. PubMed ID: 16061556
[TBL] [Abstract][Full Text] [Related]
20. Cowden syndrome.
Farooq A; Walker LJ; Bowling J; Audisio RA
Cancer Treat Rev; 2010 Dec; 36(8):577-83. PubMed ID: 20580873
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
