BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 37646013)

  • 1.
    Jensen MR; Jelsig AM; Gerdes AM; Hölmich LR; Kainu KH; Lorentzen HF; Hansen MH; Bak M; Johansson PA; Hayward NK; Van Overeem Hansen T; Wadt KAW
    HGG Adv; 2023 Oct; 4(4):100225. PubMed ID: 37646013
    [No Abstract]   [Full Text] [Related]  

  • 2. A Truncating Germline Mutation of
    He H; Li W; Comiskey DF; Liyanarachchi S; Nieminen TT; Wang Y; DeLap KE; Brock P; de la Chapelle A
    Thyroid; 2020 Feb; 30(2):204-213. PubMed ID: 31928178
    [No Abstract]   [Full Text] [Related]  

  • 3. Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
    Aoude LG; Pritchard AL; Robles-Espinoza CD; Wadt K; Harland M; Choi J; Gartside M; Quesada V; Johansson P; Palmer JM; Ramsay AJ; Zhang X; Jones K; Symmons J; Holland EA; Schmid H; Bonazzi V; Woods S; Dutton-Regester K; Stark MS; Snowden H; van Doorn R; Montgomery GW; Martin NG; Keane TM; López-Otín C; Gerdes AM; Olsson H; Ingvar C; Borg A; Gruis NA; Trent JM; Jönsson G; Bishop DT; Mann GJ; Newton-Bishop JA; Brown KM; Adams DJ; Hayward NK
    J Natl Cancer Inst; 2015 Feb; 107(2):. PubMed ID: 25505254
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility.
    Koivuluoma S; Vorimo S; Mattila TM; Tervasmäki A; Kumpula T; Kuismin O; Winqvist R; Moilanen J; Mantere T; Pylkäs K
    Fam Cancer; 2023 Jan; 22(1):13-17. PubMed ID: 35590014
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A
    Abu Shtaya A; Kedar I; Bazak L; Basel-Salmon L; Barhom SF; Naftali M; Eskin-Schwartz M; Birk OS; Polager-Modan S; Keidar N; Reznick Levi G; Levi Z; Yablonski-Peretz T; Mahamid A; Segol O; Matar R; Bareli Y; Azoulay N; Goldberg Y
    Genes (Basel); 2024 Mar; 15(3):. PubMed ID: 38540414
    [TBL] [Abstract][Full Text] [Related]  

  • 6. POT1 germline mutations but not TERT promoter mutations are implicated in melanoma susceptibility in a large cohort of Spanish melanoma families.
    Potrony M; Puig-Butille JA; Ribera-Sola M; Iyer V; Robles-Espinoza CD; Aguilera P; Carrera C; Malvehy J; Badenas C; Landi MT; Adams DJ; Puig S
    Br J Dermatol; 2019 Jul; 181(1):105-113. PubMed ID: 30451293
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtype.
    DeBoy EA; Nicosia AM; Liyanarachchi S; Iyer SS; Shah MH; Ringel MD; Brock P; Armanios M
    Am J Hum Genet; 2024 Apr; ():. PubMed ID: 38688277
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline
    Andreotti V; Vanni I; Pastorino L; Ghiorzo P; Bruno W
    Genes (Basel); 2024 Jan; 15(1):. PubMed ID: 38254993
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma.
    Wong K; Robles-Espinoza CD; Rodriguez D; Rudat SS; Puig S; Potrony M; Wong CC; Hewinson J; Aguilera P; Puig-Butille JA; Bressac-de Paillerets B; Zattara H; van der Weyden L; Fletcher CDM; Brenn T; Arends MJ; Quesada V; Newton-Bishop JA; Lopez-Otin C; Bishop DT; Harms PW; Johnson TM; Durham AB; Lombard DB; Adams DJ
    JAMA Dermatol; 2019 May; 155(5):604-609. PubMed ID: 30586141
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenita.
    Savage SA; Giri N; Jessop L; Pike K; Plona T; Burdett L; Alter BP
    J Med Genet; 2011 Apr; 48(4):285-8. PubMed ID: 21209122
    [TBL] [Abstract][Full Text] [Related]  

  • 11.
    Shen E; Xiu J; Lopez GY; Bentley R; Jalali A; Heimberger AB; Bainbridge MN; Bondy ML; Walsh KM
    J Med Genet; 2020 Oct; 57(10):664-670. PubMed ID: 31937561
    [TBL] [Abstract][Full Text] [Related]  

  • 12.
    Schmutz I; Mensenkamp AR; Takai KK; Haadsma M; Spruijt L; de Voer RM; Choo SS; Lorbeer FK; van Grinsven EJ; Hockemeyer D; Jongmans MC; de Lange T
    Elife; 2020 Dec; 9():. PubMed ID: 33258446
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of germline variants in telomere maintenance genes (
    Goldstein AM; Qin R; Chu EY; Elder DE; Massi D; Adams DJ; Harms PW; Robles-Espinoza CD; Newton-Bishop JA; Bishop DT; Harland M; Holland EA; Cust AE; Schmid H; Mann GJ; Puig S; Potrony M; Alos L; Nagore E; Millán-Esteban D; Hayward NK; Broit N; Palmer JM; Nathan V; Berry EG; Astiazaran-Symonds E; Yang XR; Tucker MA; Landi MT; Pfeiffer RM; Sargen MR
    JAAD Int; 2023 Jun; 11():43-51. PubMed ID: 36876055
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.
    Wilson TL; Hattangady N; Lerario AM; Williams C; Koeppe E; Quinonez S; Osborne J; Cha KB; Else T
    Fam Cancer; 2017 Oct; 16(4):561-566. PubMed ID: 28389767
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
    Shi J; Yang XR; Ballew B; Rotunno M; Calista D; Fargnoli MC; Ghiorzo P; Bressac-de Paillerets B; Nagore E; Avril MF; Caporaso NE; McMaster ML; Cullen M; Wang Z; Zhang X; ; ; ; Bruno W; Pastorino L; Queirolo P; Banuls-Roca J; Garcia-Casado Z; Vaysse A; Mohamdi H; Riazalhosseini Y; Foglio M; Jouenne F; Hua X; Hyland PL; Yin J; Vallabhaneni H; Chai W; Minghetti P; Pellegrini C; Ravichandran S; Eggermont A; Lathrop M; Peris K; Scarra GB; Landi G; Savage SA; Sampson JN; He J; Yeager M; Goldin LR; Demenais F; Chanock SJ; Tucker MA; Goldstein AM; Liu Y; Landi MT
    Nat Genet; 2014 May; 46(5):482-6. PubMed ID: 24686846
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a Cancer-Predisposing Germline
    Jajosky AN; Mitchell AL; Akgul M; Shetty S; Yoest JM; Gerson SL; Sadri N; Oduro KA
    Genes (Basel); 2022 Mar; 13(4):. PubMed ID: 35456397
    [TBL] [Abstract][Full Text] [Related]  

  • 17. TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes.
    Walne AJ; Vulliamy T; Beswick R; Kirwan M; Dokal I
    Blood; 2008 Nov; 112(9):3594-600. PubMed ID: 18669893
    [TBL] [Abstract][Full Text] [Related]  

  • 18. TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.
    Savage SA; Giri N; Baerlocher GM; Orr N; Lansdorp PM; Alter BP
    Am J Hum Genet; 2008 Feb; 82(2):501-9. PubMed ID: 18252230
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Population-based analysis of
    Simonin-Wilmer I; Ossio R; Leddin EM; Harland M; Pooley KA; Martil de la Garza MG; Obolenski S; Hewinson J; Wong CC; Iyer V; Taylor JC; Newton-Bishop JA; Bishop DT; Cisneros GA; Iles MM; Adams DJ; Robles-Espinoza CD
    J Med Genet; 2023 Jul; 60(7):692-696. PubMed ID: 36539277
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Constitutional variants in POT1, TERF2IP, and ACD genes in patients with melanoma in the Polish population.
    Malińska K; Deptuła J; Rogoża-Janiszewska E; Górski B; Scott R; Rudnicka H; Kashyap A; Domagała P; Hybiak J; Masojć B; Cybulski C; Kram A; Boer M; Kiedrowicz M; Lubiński J; Dębniak T
    Eur J Cancer Prev; 2020 Nov; 29(6):511-519. PubMed ID: 32976206
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.