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 *

134 related articles for article (PubMed ID: 27577212)

  • 21. Clinical and mutational heterogeneity of Darier disease in Tunisian families.
    Bchetnia M; Charfeddine C; Kassar S; Zribi H; Guettiti HT; Ellouze F; Cheour M; Boubaker S; Osman AD; Abdelhak S; Mokni M
    Arch Dermatol; 2009 Jun; 145(6):654-6. PubMed ID: 19528419
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exon 12 of the ATP2A2 gene in patients with Darier disease: one novel mutation and one previously described.
    Shi BJ; Xue M; Zhu YJ; Wang SP; Du Y; Chen DY; Diao QC
    J Eur Acad Dermatol Venereol; 2015 Feb; 29(2):394-396. PubMed ID: 24552170
    [No Abstract]   [Full Text] [Related]  

  • 23. Darier disease in Slovenia: spectrum of ATP2A2 mutations and relation to patients' phenotypes.
    Godic A; Strazisar M; Zupan A; Korosec B; Kansky A; Glavac D
    Eur J Dermatol; 2010; 20(3):271-5. PubMed ID: 20423818
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The ATP2A2 gene in patients with Darier's disease: one novel splicing mutation.
    Shi BJ; Xue M; Zhong GS; Jiang Y; Chen DY; Feng J; Hao J; Diao QC
    Int J Dermatol; 2012 Sep; 51(9):1074-7. PubMed ID: 22909361
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.
    Nellen RG; Steijlen PM; van Steensel MA; Vreeburg M; ; Frank J; van Geel M
    Hum Mutat; 2017 Apr; 38(4):343-356. PubMed ID: 28035777
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel splice-site mutation of ATP2A2 gene in a Chinese family with Darier disease.
    Huo J; Liu Y; Ma J; Xiao S
    Arch Dermatol Res; 2010 Dec; 302(10):769-72. PubMed ID: 20857128
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Darier's disease: a novel ATP2A2 missense mutation at one of the calcium-binding residues.
    Kaibuchi-Noda K; Sugiura K; Takeichi T; Miura S; Kagami S; Takama H; Hino H; Akiyama M
    Acta Derm Venereol; 2015 Mar; 95(3):362-3. PubMed ID: 24979555
    [No Abstract]   [Full Text] [Related]  

  • 28. Three novel mutations of the ATP2A2 gene in Chinese patients with Darier disease.
    Zhao Q; Fu F; Fu X; Wang Z; Liu H; Zhang F
    Australas J Dermatol; 2019 May; 60(2):e171-e172. PubMed ID: 30450560
    [No Abstract]   [Full Text] [Related]  

  • 29. 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]  

  • 30. Sporadic case of Darier disease caused by a novel splice-site mutation in the ATP2A2 gene.
    Yasuno S; Miyoshi Y; Asano N; Okita T; Yamaguchi M; Shimomura N; Kashiwagi K; Shimomura Y
    Clin Exp Dermatol; 2019 Mar; 44(2):e10-e12. PubMed ID: 30294936
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. P160L mutation in the Ca(2+) ATPase 2A domain in a patient with severe Darier disease.
    Godic A; Glavac D; Korosec B; Miljković J; Potocnik M; Kansky A
    Dermatology; 2004; 209(2):142-4. PubMed ID: 15316170
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey.
    Nakamura T; Kazuno AA; Nakajima K; Kusumi I; Tsuboi T; Kato T
    Psychiatry Clin Neurosci; 2016 Aug; 70(8):342-50. PubMed ID: 27106560
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Clinical case of acral hemorrhagic Darier's disease is not caused by mutations in exon 15 of the ATP2A2 gene.
    Pećina-Slaus N; Milavec-Puretić V; Kubat M; Furac I; Karija M; Fischer-Zigmund M; Lipozencić J
    Coll Antropol; 2003 Jun; 27(1):125-33. PubMed ID: 12974140
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Late-onset comedonal Darier's disease caused by a recurrent ATP2A2 mutation.
    Guevara BEK; Hou PC; Huang HY; Chen WR; Wen YK; Chen WC; Lee JY; Hsu CK
    J Dermatol; 2019 Jun; 46(6):e211-e212. PubMed ID: 30663125
    [No Abstract]   [Full Text] [Related]  

  • 37. Genetic heterogeneity in acrokeratosis verruciformis of Hopf.
    Wang PG; Gao M; Lin GS; Yang S; Lin D; Liang YH; Zhang GL; Zhu YG; Cui Y; Zhang KY; Huang W; Zhang XJ
    Clin Exp Dermatol; 2006 Jul; 31(4):558-63. PubMed ID: 16716163
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel mutation in the ATP2A2 gene in a Japanese Darier's disease patient with extremely hyperkeratotic lesions.
    Miyabe C; Mitsuhashi Y; Saito M; Tsuboi R
    J Dermatol; 2012 Apr; 39(4):401-3. PubMed ID: 22035154
    [No Abstract]   [Full Text] [Related]  

  • 39. A novel ATP2A2 missense mutation p.Asp254Gly in Darier disease restricted to the extremities.
    Moriuchi R; Akiyama M; Onozuka T; Shimizu H
    J Am Acad Dermatol; 2008 May; 58(5 Suppl 1):S116-8. PubMed ID: 18489043
    [No Abstract]   [Full Text] [Related]  

  • 40. A Postzygotic ATP2A2 Novel Mutation Identified by Next-generation Sequencing in Mosaic Darier Disease.
    Guerra L; Pedicelli C; Proto V; Condorelli AG; Mazzanti C; Castiglia D
    Acta Derm Venereol; 2019 Jan; 99(1):115-116. PubMed ID: 30085326
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.