121 related articles for article (PubMed ID: 29956681)
1. Novel mutations in
Zhong WL; Wang HJ; Lin ZM; Yang Y
Indian J Dermatol Venereol Leprol; 2019; 85(4):440. PubMed ID: 29956681
[No Abstract] [Full Text] [Related]
2. Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria.
Liu JW; Habulieti X; Wang RR; Ma DL; Zhang X
J Clin Lab Anal; 2021 Jun; 35(6):e23803. PubMed ID: 34028087
[TBL] [Abstract][Full Text] [Related]
3. Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria.
Lu C; Liu J; Liu F; Liu Y; Ma D; Zhang X
J Dermatol Sci; 2014 Dec; 76(3):255-8. PubMed ID: 25288164
[No Abstract] [Full Text] [Related]
4. Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation.
Zhong W; Pan Y; Shao Y; Yang Y; Yu B; Lin Z
Clin Exp Dermatol; 2019 Apr; 44(3):e58-e60. PubMed ID: 30430618
[No Abstract] [Full Text] [Related]
5. Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria.
Cao L; Zhang R; Yong L; Chen S; Zhang H; Chen W; Xu Q; Ge H; Mao Y; Zhen Q; Yu Y; Hu X; Sun L
BMC Med Genomics; 2021 Jun; 14(1):168. PubMed ID: 34174894
[TBL] [Abstract][Full Text] [Related]
6. A novel P53/POMC/Gαs/SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation.
Zhou D; Wei Z; Kuang Z; Luo H; Ma J; Zeng X; Wang K; Liu B; Gong F; Wang J; Lei S; Wang D; Zeng J; Wang T; He Y; Yuan Y; Dai H; He L; Xing Q
J Cell Mol Med; 2017 Apr; 21(4):802-815. PubMed ID: 27885802
[TBL] [Abstract][Full Text] [Related]
7. Mutated SASH1 promotes Mitf expression in a heterozygous mutated SASH1 knock‑in mouse model.
Xu Z; Li Y; Wang D; Wu D; Wang J; Chen L; Deng Y; Zhang J; Wu Z; Wan X; Liu Q; Huang H; Hu P; Zeng J; Zhou D
Int J Mol Med; 2020 Sep; 46(3):1118-1134. PubMed ID: 32582980
[TBL] [Abstract][Full Text] [Related]
8. p53 regulates ERK1/2/CREB cascade via a novel SASH1/MAP2K2 crosstalk to induce hyperpigmentation.
Zhou D; Kuang Z; Zeng X; Wang K; Ma J; Luo H; Chen M; Li Y; Zeng J; Li S; Luan F; He Y; Dai H; Liu B; Li H; He L; Xing Q
J Cell Mol Med; 2017 Oct; 21(10):2465-2480. PubMed ID: 28382689
[TBL] [Abstract][Full Text] [Related]
9. Updated review of genetic reticulate pigmentary disorders.
Zhang J; Li M; Yao Z
Br J Dermatol; 2017 Oct; 177(4):945-959. PubMed ID: 28407215
[TBL] [Abstract][Full Text] [Related]
10. Ultrastructural Investigations in an Autosomal Recessively Inherited Case of Dyschromatosis Universalis Hereditaria.
Gupta A; Sharma Y; Dash KN; Verma S; Natarajan VT; Singh A
Acta Derm Venereol; 2015 Jul; 95(6):738-40. PubMed ID: 25474346
[No Abstract] [Full Text] [Related]
11. Dyschromatosis universalis hereditaria: a rare entity.
Kumar S; Mahajan BB; Singh R
Dermatol Online J; 2011 Jul; 17(7):6. PubMed ID: 21810391
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.
Liu H; Li Y; Hung KK; Wang N; Wang C; Chen X; Sheng D; Fu X; See K; Foo JN; Low H; Liany H; Irwan ID; Liu J; Yang B; Chen M; Yu Y; Yu G; Niu G; You J; Zhou Y; Ma S; Wang T; Yan X; Goh BK; Common JE; Lane BE; Sun Y; Zhou G; Lu X; Wang Z; Tian H; Cao Y; Chen S; Liu Q; Liu J; Zhang F
PLoS One; 2014; 9(2):e87250. PubMed ID: 24498303
[TBL] [Abstract][Full Text] [Related]
13. Four novel and two recurrent mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria.
Wang XP; Wang WJ; Wang JM; Liu Y; Xiao SX
J Dermatol Sci; 2010 Jun; 58(3):217-8. PubMed ID: 20430589
[No Abstract] [Full Text] [Related]
14. A novel missense mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
Dong Y; Xiao S; Ren J; Huo J; Liu Y; Li X
Eur J Dermatol; 2009; 19(3):270-2. PubMed ID: 19251566
[No Abstract] [Full Text] [Related]
15. Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.
Cui YX; Xia XY; Zhou Y; Gao L; Shang XJ; Ni T; Wang WP; Fan XB; Yin HL; Jiang SJ; Yao B; Hu YA; Wang G; Li XJ
PLoS One; 2013; 8(11):e79808. PubMed ID: 24224009
[TBL] [Abstract][Full Text] [Related]
16. Dyschromatosis universalis hereditaria: report of six cases from a family.
Sardar SK; Das A; Bandyopadhyay DB
Dermatol Online J; 2016 Sep; 22(9):. PubMed ID: 28329614
[TBL] [Abstract][Full Text] [Related]
17. Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria.
Binitha MP; Thomas D; Asha LK
Indian J Dermatol Venereol Leprol; 2006; 72(4):300-2. PubMed ID: 16880579
[TBL] [Abstract][Full Text] [Related]
18. Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene.
Murata I; Hayashi M; Hozumi Y; Fujii K; Mitsuhashi Y; Oiso N; Fukai K; Kuroki N; Mori Y; Utani A; Tomita Y; Fujita Y; Suzuki T
J Dermatol Sci; 2010 Jun; 58(3):218-20. PubMed ID: 20439151
[No Abstract] [Full Text] [Related]
19. Mutations in ABCB6 cause dyschromatosis universalis hereditaria.
Zhang C; Li D; Zhang J; Chen X; Huang M; Archacki S; Tian Y; Ren W; Mei A; Zhang Q; Fang M; Su Z; Yin Y; Liu D; Chen Y; Cui X; Li C; Yang H; Wang Q; Wang J; Liu M; Deng Y
J Invest Dermatol; 2013 Sep; 133(9):2221-8. PubMed ID: 23519333
[TBL] [Abstract][Full Text] [Related]
20. Uncovering a new SASH1 mutation associated with dyschromatosis universalis hereditaria using whole-exome-sequencing: A case report.
Yang Y; Jiang N; Mai JQ; Yang S; Xiao Y; Liu S
Medicine (Baltimore); 2023 Aug; 102(31):e34448. PubMed ID: 37543808
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]