These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 22572734)

  • 21. PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome.
    Gielen RCAM; Reinders MGHC; Koillinen HK; Paulussen ADC; Mosterd K; van Geel M
    J Hum Genet; 2018 Sep; 63(9):965-969. PubMed ID: 29930296
    [TBL] [Abstract][Full Text] [Related]  

  • 22. PTCH1 and SMO gene alterations in keratocystic odontogenic tumors.
    Sun LS; Li XF; Li TJ
    J Dent Res; 2008 Jun; 87(6):575-9. PubMed ID: 18502968
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Is PATCHED an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report.
    Roudgari H; Farndon PA; Murray AD; Hardy C; Miedzybrodzka Z
    Clin Genet; 2012 Jul; 82(1):71-6. PubMed ID: 21651513
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Myogenic tumors in nevoid Basal cell carcinoma syndrome.
    Hettmer S; Teot LA; Kozakewich H; Werger AM; Davies KJ; Fletcher CD; Grier HE; Rodriguez-Galindo C; Wagers AJ
    J Pediatr Hematol Oncol; 2015 Mar; 37(2):147-9. PubMed ID: 24517962
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.
    Pastorino L; Cusano R; Nasti S; Faravelli F; Forzano F; Baldo C; Barile M; Gliori S; Muggianu M; Ghigliotti G; Lacaita MG; Lo Muzio L; Bianchi-Scarra G
    Hum Mutat; 2005 Mar; 25(3):322-3. PubMed ID: 15712338
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. PTCH1 mutations in odontogenic keratocysts: are they related to epithelial cell proliferation?
    Pan S; Li TJ
    Oral Oncol; 2009 Oct; 45(10):861-5. PubMed ID: 19362041
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome.
    Le Brun Keris Y; Jouk PS; Saada-Sebag G; Roux JJ; Mattei B; Bagait L; Paoloni-Giacobino A; Grandchamp B; Soufir N; Lespinasse J
    Eur J Med Genet; 2008; 51(5):472-8. PubMed ID: 18539553
    [TBL] [Abstract][Full Text] [Related]  

  • 29.
    Ponti G; Manfredini M; Pastorino L; Maccaferri M; Tomasi A; Pellacani G
    Anticancer Res; 2018 Jan; 38(1):471-476. PubMed ID: 29277811
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Somatic mosaicism containing double mutations in
    Ikemoto Y; Takayama Y; Fujii K; Masuda M; Kato C; Hatsuse H; Fujitani K; Nagao K; Kameyama K; Ikehara H; Toyoda M; Umezawa A; Miyashita T
    J Med Genet; 2017 Aug; 54(8):579-584. PubMed ID: 28363938
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Biallelic disruption of the PTCH1 gene in multiple basal cell carcinomas in Japanese patients with nevoid basal cell carcinoma syndrome.
    Tate G; Kishimoto K; Mitsuya T
    Acta Med Okayama; 2014; 68(3):163-70. PubMed ID: 24942795
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Ultraviolet responses of Gorlin syndrome primary skin cells.
    Brellier F; Valin A; Chevallier-Lagente O; Gorry P; Avril MF; Magnaldo T
    Br J Dermatol; 2008 Aug; 159(2):445-52. PubMed ID: 18510667
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles.
    Savino M; d'Apolito M; Formica V; Baorda F; Mari F; Renieri A; Carabba E; Tarantino E; Andreucci E; Belli S; Lo Muzio L; Dallapiccola B; Zelante L; Savoia A
    Hum Mutat; 2004 Nov; 24(5):441. PubMed ID: 15459969
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.
    Honma M; Ohishi Y; Uehara J; Ibe M; Kinouchi M; Ishida-Yamamoto A; Iizuka H
    J Dermatol Sci; 2008 Apr; 50(1):73-5. PubMed ID: 18068337
    [No Abstract]   [Full Text] [Related]  

  • 36. Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data.
    Gianferante DM; Rotunno M; Dean M; Zhou W; Hicks BD; Wyatt K; Jones K; Wang M; Zhu B; Goldstein AM; Mirabello L
    Mol Genet Genomic Med; 2018 Nov; 6(6):1168-1180. PubMed ID: 30411536
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations: a case report.
    Sasaki R; Miyashita T; Matsumoto N; Fujii K; Saito K; Ando T
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 Aug; 110(2):e41-6. PubMed ID: 20659694
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Regulation of human PTCH1b expression by different 5' untranslated region cis-regulatory elements.
    Ozretić P; Bisio A; Musani V; Trnski D; Sabol M; Levanat S; Inga A
    RNA Biol; 2015; 12(3):290-304. PubMed ID: 25826662
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome.
    Matsuzawa N; Nagao T; Shimozato K; Niikawa N; Yoshiura KI
    J Clin Pathol; 2006 Oct; 59(10):1084-6. PubMed ID: 17021131
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.
    Garavelli L; Piemontese MR; Cavazza A; Rosato S; Wischmeijer A; Gelmini C; Albertini E; Albertini G; Forzano F; Franchi F; Carella M; Zelante L; Superti-Furga A
    Am J Med Genet A; 2013 Nov; 161A(11):2894-901. PubMed ID: 24124115
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.