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 *

157 related articles for article (PubMed ID: 37460876)

  • 1. Establishment of induced pluripotent stem cells derived from patients and healthy siblings of a nevoid basal cell carcinoma syndrome family.
    Nakase Y; Hamada A; Obayashi F; Kitamura N; Hata T; Yamamoto T; Okamoto T
    In Vitro Cell Dev Biol Anim; 2023 Jun; 59(6):395-400. PubMed ID: 37460876
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4.
    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]  

  • 5. A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome.
    Zhou J; Zhang G; Shi M; Liu Z; Xiao M; Fu S; Gong X; Shi X
    Med Mol Morphol; 2019 Dec; 52(4):235-237. PubMed ID: 30997576
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterozygous PTCH1 Mutations Impact the Bone Metabolism in Patients With Nevoid Basal Cell Carcinoma Syndrome Likely by Regulating SPARC Expression.
    Hong Y; Zhang J; Zhang H; Li X; Qu J; Zhai J; Zhang L; Chen F; Li T
    J Bone Miner Res; 2016 Jul; 31(7):1413-28. PubMed ID: 26890308
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mechanisms of inactivation of PTCH1 gene in nevoid basal cell carcinoma syndrome: modification of the two-hit hypothesis.
    Pan S; Dong Q; Sun LS; Li TJ
    Clin Cancer Res; 2010 Jan; 16(2):442-50. PubMed ID: 20068110
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients: two familial and three sporadic cases including the first Japanese patient with medulloblastoma.
    Fujii M; Noguchi K; Urade M; Muraki Y; Moridera K; Kishimoto H; Hashimoto-Tamaoki T; Nakano Y
    J Hum Genet; 2011 Apr; 56(4):277-83. PubMed ID: 21368767
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel PTCH1 mutations in Japanese familial nevoid basal cell carcinoma syndrome.
    Nakase Y; Hamada A; Kitamura N; Hata T; Toratani S; Yamamoto T; Okamoto T
    Hum Genome Var; 2020 Nov; 7(1):38. PubMed ID: 33298892
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The large intracellular loop of ptch1 mediates the non-canonical Hedgehog pathway through cyclin B1 in nevoid basal cell carcinoma syndrome.
    Yu FY; Hong YY; Qu JF; Chen F; Li TJ
    Int J Mol Med; 2014 Aug; 34(2):507-12. PubMed ID: 24840883
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome.
    Alonso N; Cañueto J; Ciria S; Bueno E; Palacios-Alvarez I; Alegre M; Badenas C; Barreiro A; Pena L; Maldonado C; Nespeira-Jato MV; Peña-Penabad C; Azon A; Gavrilova M; Ferrer I; Sanmartin O; Robles L; Hernandez-Martin A; Urioste M; Puig S; Puig L; Gonzalez-Sarmiento R
    Br J Dermatol; 2018 Jan; 178(1):198-206. PubMed ID: 28733979
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome.
    Pastorino L; Pollio A; Pellacani G; Guarneri C; Ghiorzo P; Longo C; Bruno W; Giusti F; Bassoli S; Bianchi-Scarrà G; Ruini C; Seidenari S; Tomasi A; Ponti G
    PLoS One; 2012; 7(8):e43827. PubMed ID: 22952776
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. PTCH1 gene mutations in Keratocystic odontogenic tumors: a study of 43 Chinese patients and a systematic review.
    Guo YY; Zhang JY; Li XF; Luo HY; Chen F; Li TJ
    PLoS One; 2013; 8(10):e77305. PubMed ID: 24204797
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population.
    Lu N; Wang J; Zhu B; Zhang M; Qi F; Wang X; Gu J
    Cancer Biomark; 2017 Dec; 21(1):161-168. PubMed ID: 29081410
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 5-aminolevulinic acid photodynamic therapy and excision surgery for nevoid basal cell carcinoma syndrome with multiple basal cell carcinomas and PTCH1 mutation.
    Li C; Chen P; Li Z; Wang Y; He S; Shi M; Wang Q; Xu M; Li Q; Chen H; Zeng K; Liang J; Zhang X
    Photodiagnosis Photodyn Ther; 2020 Dec; 32():101968. PubMed ID: 32835883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation.
    Rodrigues AL; Carvalho A; Cabral R; Carneiro V; Gilardi P; Duarte CP; Puente-Prieto J; Santos P; Mota-Vieira L
    Genet Mol Res; 2014 Jul; 13(3):5654-63. PubMed ID: 25117323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. PTCH1 +/- dermal fibroblasts isolated from healthy skin of Gorlin syndrome patients exhibit features of carcinoma associated fibroblasts.
    Valin A; Barnay-Verdier S; Robert T; Ripoche H; Brellier F; Chevallier-Lagente O; Avril MF; Magnaldo T
    PLoS One; 2009; 4(3):e4818. PubMed ID: 19287498
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.