BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 34990798)

  • 1. Inherited rare and common variants in PTCH1 and PTCH2 contributing to the predisposition to reproductive cancers.
    Yang XH; Xu BH; Zhou DL; Long YK; Liu Q; Huang C; Ye ZL; He CY
    Gene; 2022 Mar; 814():146157. PubMed ID: 34990798
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Patched-2 functions to limit Patched-1 deficient skin cancer growth.
    Veenstra VL; Dingjan I; Waasdorp C; Damhofer H; van der Wal AC; van Laarhoven HW; Medema JP; Bijlsma MF
    Cell Oncol (Dordr); 2018 Aug; 41(4):427-437. PubMed ID: 29869097
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital embryonal rhabdomyosarcoma caused by heterozygous concomitant PTCH1 and PTCH2 germline mutations.
    Taeubner J; Brozou T; Qin N; Bartl J; Ginzel S; Schaper J; Felsberg J; Fulda S; Vokuhl C; Borkhardt A; Kuhlen M
    Eur J Hum Genet; 2018 Jan; 26(1):137-142. PubMed ID: 29230040
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The protein-specific activities of the transmembrane modules of Ptch1 and Ptch2 are determined by their adjacent protein domains.
    Fleet AJ; Hamel PA
    J Biol Chem; 2018 Oct; 293(43):16583-16595. PubMed ID: 30166346
    [TBL] [Abstract][Full Text] [Related]  

  • 5. PTCH2 is not a strong candidate gene for gorlin syndrome predisposition.
    Smith MJ; Evans DG
    Fam Cancer; 2022 Jul; 21(3):343-346. PubMed ID: 34170463
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Patched2 modulates tumorigenesis in patched1 heterozygous mice.
    Lee Y; Miller HL; Russell HR; Boyd K; Curran T; McKinnon PJ
    Cancer Res; 2006 Jul; 66(14):6964-71. PubMed ID: 16849540
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.
    Casano K; Meddaugh H; Zambrano RM; Marble M; Torres JI; Lacassie Y
    Eur J Med Genet; 2020 Apr; 63(4):103842. PubMed ID: 31945512
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distinct roles of PTCH2 splice variants in Hedgehog signalling.
    Rahnama F; Toftgård R; Zaphiropoulos PG
    Biochem J; 2004 Mar; 378(Pt 2):325-34. PubMed ID: 14613484
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.
    Onodera S; Saito A; Hasegawa D; Morita N; Watanabe K; Nomura T; Shibahara T; Ohba S; Yamaguchi A; Azuma T
    PLoS One; 2017; 12(9):e0184702. PubMed ID: 28915250
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PTCH2, a novel human patched gene, undergoing alternative splicing and up-regulated in basal cell carcinomas.
    Zaphiropoulos PG; Undén AB; Rahnama F; Hollingsworth RE; Toftgård R
    Cancer Res; 1999 Feb; 59(4):787-92. PubMed ID: 10029063
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.
    Fujii K; Ohashi H; Suzuki M; Hatsuse H; Shiohama T; Uchikawa H; Miyashita T
    Fam Cancer; 2013 Dec; 12(4):611-4. PubMed ID: 23479190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [PTCH2 gene alterations in keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome].
    Xu LL; Li TJ
    Beijing Da Xue Xue Bao Yi Xue Ban; 2008 Feb; 40(1):15-8. PubMed ID: 18278130
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Essential role for ligand-dependent feedback antagonism of vertebrate hedgehog signaling by PTCH1, PTCH2 and HHIP1 during neural patterning.
    Holtz AM; Peterson KA; Nishi Y; Morin S; Song JY; Charron F; McMahon AP; Allen BL
    Development; 2013 Aug; 140(16):3423-34. PubMed ID: 23900540
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ptch2 shares overlapping functions with Ptch1 in Smo regulation and limb development.
    Zhulyn O; Nieuwenhuis E; Liu YC; Angers S; Hui CC
    Dev Biol; 2015 Jan; 397(2):191-202. PubMed ID: 25448692
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome.
    Matsudate Y; Naruto T; Hayashi Y; Minami M; Tohyama M; Yokota K; Yamada D; Imoto I; Kubo Y
    J Dermatol Sci; 2017 Jun; 86(3):206-211. PubMed ID: 28342698
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of rare variants in PTCH2 associated with non-syndromic orofacial clefts.
    Liang X; He Q; Jiao Y; Yang H; Huang W; Liu K; Lin H; Xu L; Hou Y; Ding Y; Zhang Y; Huang H; Zhao H
    Gene; 2024 May; 907():148280. PubMed ID: 38360123
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ptch2/Gas1 and Ptch1/Boc differentially regulate Hedgehog signalling in murine primordial germ cell migration.
    Kim Y; Lee J; Seppala M; Cobourne MT; Kim SH
    Nat Commun; 2020 Apr; 11(1):1994. PubMed ID: 32332736
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nevoid Basal Cell Carcinoma Syndrome:
    Martinez MF; Romano MV; Martinez AP; González A; Muchnik C; Stengel FM; Mazzuoccolo LD; Azurmendi PJ
    Cells; 2019 Feb; 8(2):. PubMed ID: 30754660
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome.
    Durmaz CD; Evans G; Smith MJ; Ertop P; Akay BN; Tuncalı T
    Cytogenet Genome Res; 2018; 154(2):57-61. PubMed ID: 29544218
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expression pattern of Ptch2 in mouse embryonic maxillofacial development.
    Wang X; Ma Z; Wu Y; Chen J; Peng X; Wang Y; Fan M; Du J
    Acta Histochem; 2022 Jan; 124(1):151835. PubMed ID: 34979374
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.