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 *

141 related articles for article (PubMed ID: 27107679)

  • 1. Wall paintings facies and their possible genetic correlates in the ancient Pompeii: A bio-anthropologic message from the past?
    Ponti G; Manfredini M; Ruini C
    Gene; 2016 Sep; 589(2):151-6. PubMed ID: 27107679
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Skeletal stigmata as keys to access to the composite and ancient Gorlin-Goltz syndrome history: The Egypt, Pompeii and Herculaneum lessons.
    Ponti G; Pellacani G; Tomasi A; Sammaria G; Manfredini M
    Gene; 2016 Sep; 589(2):104-11. PubMed ID: 26794802
    [TBL] [Abstract][Full Text] [Related]  

  • 3.
    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]  

  • 4. Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation.
    Ponti G; Ruini C; Pastorino L; Loschi P; Pecchi A; Malagoli M; Mandel VD; Boano R; Conti A; Pellacani G; Tomasi A
    Future Oncol; 2014 May; 10(6):917-25. PubMed ID: 24941978
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Ocular manifestations in Gorlin-Goltz syndrome.
    Moramarco A; Himmelblau E; Miraglia E; Mallone F; Roberti V; Franzone F; Iacovino C; Giustini S; Lambiase A
    Orphanet J Rare Dis; 2019 Sep; 14(1):218. PubMed ID: 31533758
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nevoid basal cell carcinoma syndrome (Gorlin syndrome).
    Lo Muzio L
    Orphanet J Rare Dis; 2008 Nov; 3():32. PubMed ID: 19032739
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Nevoid basal cell carcinoma syndrome with corpus callosum agenesis, PTCH1 mutation and absence of basal cell carcinoma].
    Mazzuoccolo LD; Martínez MF; Muchnik C; Azurmendi PJ; Stengel F
    Medicina (B Aires); 2014; 74(4):307-10. PubMed ID: 25188659
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Skeletal and dermatological manifestations of the nevoid Basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Results of 8 patients in 12 years].
    Rupprecht M; Mensing CH; Barvencik F; Ittrich H; Heiland M; Rueger JM; Amling M; Pogoda P
    Rofo; 2007 Jun; 179(6):618-26. PubMed ID: 17492539
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genodermatoses among the ancients: basal cell nevus syndrome in Egyptian dynastic brothers.
    Lowenstein EJ
    Skinmed; 2011; 9(2):117-8. PubMed ID: 21548519
    [No Abstract]   [Full Text] [Related]  

  • 14. Genetic and clinicopathologic aspects of Gorlin-Goltz syndrome (NBCCS): presentation of two case reports and literature review.
    Acocella A; Sacco R; Bertolai R; Sacco N
    Minerva Stomatol; 2009; 58(1-2):43-53. PubMed ID: 19234436
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.
    Musani V; Ozretić P; Trnski D; Sabol M; Poduje S; Tošić M; Šitum M; Levanat S
    Croat Med J; 2018 Feb; 59(1):20-24. PubMed ID: 29498494
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Unexpected phenotype in a frameshift mutation of PTCH1.
    Beltrami B; Prada E; Tolva G; Scuvera G; Silipigni R; Graziani D; Bulfamante G; Gervasini C; Marchisio P; Milani D
    Mol Genet Genomic Med; 2020 Jan; 8(1):e987. PubMed ID: 31578813
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.