209 related articles for article (PubMed ID: 16541093)
21. Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier's disease.
Klausegger A; Nischler E; Wagner RN; Pletschacher F; Hintner H; Bauer JW
Arch Dermatol Res; 2011 Jul; 303(5):371-4. PubMed ID: 21519848
[TBL] [Abstract][Full Text] [Related]
22. Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder.
Jacobsen NJ; Franks EK; Elvidge G; Jones I; McCandless F; O'Donovan MC; Owen MJ; Craddock N
Mol Psychiatry; 2001 Jan; 6(1):92-7. PubMed ID: 11244492
[TBL] [Abstract][Full Text] [Related]
23. SERCA2 Haploinsufficiency in a Mouse Model of Darier Disease Causes a Selective Predisposition to Heart Failure.
Prasad V; Lorenz JN; Lasko VM; Nieman ML; Huang W; Wang Y; Wieczorek DW; Shull GE
Biomed Res Int; 2015; 2015():251598. PubMed ID: 26064889
[TBL] [Abstract][Full Text] [Related]
24. Expression of SERCA2 (Darier's disease gene product) in acantholytic dermatoses.
Porgpermdee S; Takagi A; Mayuzumi N; Ogawa H; Ikeda S; Nakamura S
J Dermatol Sci; 2006 Aug; 43(2):146-9. PubMed ID: 16675202
[No Abstract] [Full Text] [Related]
25. Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier's disease, causes behavioral abnormalities and a hyper-dopaminergic state.
Nakajima K; Ishiwata M; Weitemier AZ; Shoji H; Monai H; Miyamoto H; Yamakawa K; Miyakawa T; McHugh TJ; Kato T
Hum Mol Genet; 2021 Aug; 30(18):1762-1772. PubMed ID: 34104969
[TBL] [Abstract][Full Text] [Related]
26. Novel mutations of ATP2A2 gene in Japanese patients of Darier's disease.
Takahashi H; Atsuta Y; Sato K; Ishida-Yamamoto A; Suzuki H; Iizuka H
J Dermatol Sci; 2001 Jul; 26(3):169-72. PubMed ID: 11390201
[TBL] [Abstract][Full Text] [Related]
27. Mutations in ATP2A2 in patients with Darier's disease.
Ikeda S; Mayuzumi N; Shigihara T; Epstein EH; Goldsmith LA; Ogawa H
J Invest Dermatol; 2003 Sep; 121(3):475-7. PubMed ID: 12925202
[No Abstract] [Full Text] [Related]
28. Identification of mutations in the ATP2A2 gene in patients with Darier's disease from Hungary.
Rácz E; Csikós M; Kornsée Z; Horváth A; Kárpáti S
Exp Dermatol; 2004 Jun; 13(6):396-9. PubMed ID: 15186327
[TBL] [Abstract][Full Text] [Related]
29. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.
Jacobsen NJ; Lyons I; Hoogendoorn B; Burge S; Kwok PY; O'Donovan MC; Craddock N; Owen MJ
Hum Mol Genet; 1999 Sep; 8(9):1631-6. PubMed ID: 10441325
[TBL] [Abstract][Full Text] [Related]
30. Mosaicism for ATP2A2 mutations causes segmental Darier's disease.
Sakuntabhai A; Dhitavat J; Burge S; Hovnanian A
J Invest Dermatol; 2000 Dec; 115(6):1144-7. PubMed ID: 11121153
[TBL] [Abstract][Full Text] [Related]
31. ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.
Ruiz-Perez VL; Carter SA; Healy E; Todd C; Rees JL; Steijlen PM; Carmichael AJ; Lewis HM; Hohl D; Itin P; Vahlquist A; Gobello T; Mazzanti C; Reggazini R; Nagy G; Munro CS; Strachan T
Hum Mol Genet; 1999 Sep; 8(9):1621-30. PubMed ID: 10441324
[TBL] [Abstract][Full Text] [Related]
32. Novel ATP2A2 mutation in a patient with Darier's disease.
Yoneda K; Demitsu T; Kubota Y
J Dermatol; 2014 Apr; 41(4):349-50. PubMed ID: 24612043
[No Abstract] [Full Text] [Related]
33. Mutation analysis of the ATP2A2 gene in Taiwanese patients with Darier's disease.
Chao SC; Yang MH; Lee JY
Br J Dermatol; 2002 Jun; 146(6):958-63. PubMed ID: 12072062
[TBL] [Abstract][Full Text] [Related]
34. Identification a novel missense mutation p.R761L in Chinese patients with Darier's disease.
Song J; Li M; Yang LJ; Zhang GL
Arch Dermatol Res; 2010 May; 302(4):311-4. PubMed ID: 20204653
[TBL] [Abstract][Full Text] [Related]
35. Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier's disease.
Tavadia S; Authi KS; Hodgins MB; Munro CS
Br J Dermatol; 2004 Aug; 151(2):440-5. PubMed ID: 15327552
[TBL] [Abstract][Full Text] [Related]
36. Identification of mutation c.632G>A (p.G211D) in the ATP2A2 gene and genotype-phenotype correlation in a large Chinese family with Darier's disease.
Lu FY; Xu L; Yin XG; Wan P; Zhang XD; Chen WW; Ding SP; Yao YG
Int J Dermatol; 2011 Nov; 50(11):1366-1370. PubMed ID: 22004489
[TBL] [Abstract][Full Text] [Related]
37. Three novel mutations in the ATP2A2 gene in Hungarian families with Darier's disease, including a novel splice site generating intronic nucleotide change.
Racz E; Csikós M; Benko R; Kornseé Z; Kárpáti S
J Dermatol Sci; 2005 Jun; 38(3):231-4. PubMed ID: 15927817
[No Abstract] [Full Text] [Related]
38. Exacerbation, then clearance, of mutation-proven Darier's disease of the skin after radiotherapy for bronchial carcinoma: a case of radiation-induced epidermal differentiation?
Mac Manus MP; Cavalleri G; Ball DL; Beasley M; Rotstein H; McKay MJ
Radiat Res; 2001 Dec; 156(6):724-30. PubMed ID: 11741496
[TBL] [Abstract][Full Text] [Related]
39. ER-to-Golgi blockade of nascent desmosomal cadherins in SERCA2-inhibited keratinocytes: Implications for Darier's disease.
Li N; Park M; Xiao S; Liu Z; Diaz LA
Traffic; 2017 Apr; 18(4):232-241. PubMed ID: 28156030
[TBL] [Abstract][Full Text] [Related]
40. Endoplasmic reticulum calcium, stress, and cell-to-cell adhesion.
Mauro T
J Invest Dermatol; 2014 Jul; 134(7):1800-1801. PubMed ID: 24924761
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
