435 related articles for article (PubMed ID: 28342698)
1. 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]
2. Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome.
Morita K; Naruto T; Tanimoto K; Yasukawa C; Oikawa Y; Masuda K; Imoto I; Inazawa J; Omura K; Harada H
PLoS One; 2015; 10(11):e0140480. PubMed ID: 26544948
[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. 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]
5. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.
Hasan Ali O; Yurchenko AA; Pavlova O; Sartori A; Bomze D; Higgins R; Ring SS; Hartmann F; Bühler D; Fritzsche FR; Jochum W; Navarini AA; Kim A; French LE; Dermitzakis E; Christiano AM; Hohl D; Bickers DR; Nikolaev SI; Flatz L
J Eur Acad Dermatol Venereol; 2021 Feb; 35(2):396-402. PubMed ID: 32564428
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing.
Kim B; Kim MJ; Hur K; Jo SJ; Ko JM; Park SS; Seong MW; Mun JH
Sci Rep; 2021 Jan; 11(1):1163. PubMed ID: 33441926
[TBL] [Abstract][Full Text] [Related]
8. 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]
9.
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]
10. Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome.
Kosaki R; Nagao K; Kameyama K; Suzuki M; Fujii K; Miyashita T
Am J Med Genet A; 2012 Jul; 158A(7):1724-8. PubMed ID: 22711650
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular pathogenesis of keratocystic odontogenic tumors developing in nevoid basal cell carcinoma syndrome.
Suzuki M; Nagao K; Hatsuse H; Sasaki R; Saito K; Fujii K; Miyashita T
Oral Surg Oral Med Oral Pathol Oral Radiol; 2013 Sep; 116(3):348-53. PubMed ID: 23953420
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
[TBL] [Abstract][Full Text] [Related]
17. High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndrome.
Fujii K; Ishikawa S; Uchikawa H; Komura D; Shapero MH; Shen F; Hung J; Arai H; Tanaka Y; Sasaki K; Kohno Y; Yamada M; Jones KW; Aburatani H; Miyashita T
Hum Genet; 2007 Dec; 122(5):459-66. PubMed ID: 17703323
[TBL] [Abstract][Full Text] [Related]
18. Polydactyly Patient Carried a Mutation of
Cao R; Liu S; Chai W; Shen P
DNA Cell Biol; 2020 Oct; 39(10):1754-1759. PubMed ID: 32716646
[TBL] [Abstract][Full Text] [Related]
19. Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.
Kijima C; Miyashita T; Suzuki M; Oka H; Fujii K
Fam Cancer; 2012 Dec; 11(4):565-70. PubMed ID: 22829011
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]