Found: 22
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A novel missense mutation in ADAR1 gene causing dyschromatosis symmetrica hereditaria in a Chinese patient.
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2015, v. 81, n. 3, p. 327, doi. 10.4103/0378-6323.155560
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- Article
Mal de Meleda with homozygous mutation p.G86R in SLURP‐1.
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- International Journal of Dermatology, 2020, v. 59, n. 6, p. 751, doi. 10.1111/ijd.14807
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- Publication type:
- Article
Inhibition of MITF and Tyrosinase by Paeonol-Stimulated JNK/SAPK to Reduction of Phosphorylated CREB.
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- American Journal of Chinese Medicine, 2008, v. 36, n. 2, p. 245, doi. 10.1142/S0192415X08005758
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- Article
A Gene Locus Responsible for Reticulate Pigmented Anomaly of the Flexures Maps to Chromosome 17p13.3.
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- Journal of Investigative Dermatology, 2006, v. 126, n. 6, p. 1297, doi. 10.1038/sj.jid.5700271
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- Publication type:
- Article
Identification of a Locus for Punctate Palmoplantar Keratodermas at Chromosome 8q24.13–8q24.21.
- Published in:
- Journal of Investigative Dermatology, 2004, v. 122, n. 5, p. 1121, doi. 10.1111/j.0022-202X.2004.22507.x
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- Publication type:
- Article
Identification of a Locus for Dyschromatosis Symmetrica Hereditaria at Chromosome 1q11–1q21.
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- Journal of Investigative Dermatology, 2003, v. 120, n. 5, p. 776, doi. 10.1046/j.1523-1747.2003.12130.x
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- Publication type:
- Article
Identification of a novel mutation in a Chinese patient with mild Darier's disease Li et al. Novel mutation in Darier's disease.
- Published in:
- International Journal of Dermatology, 2010, v. 49, n. 11, p. 1286, doi. 10.1111/j.1365-4632.2009.04159.x
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- Publication type:
- Article
Acquired latent tuberculosis infection in psoriasis patients treated with etanercept in the People's Republic of China.
- Published in:
- Drug Design, Development & Therapy, 2015, v. 9, p. 5591, doi. 10.2147/DDDT.S87260
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- Article
A modified method for purifying amelanotic melanocytes from human hair follicles.
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- Journal of Dermatology, 2006, v. 33, n. 4, p. 239, doi. 10.1111/j.1346-8138.2006.00059.x
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- Publication type:
- Article
Endothelin-1 combined with extracellular matrix proteins promotes the adhesion and chemotaxis of amelanotic melanocytes from human hair follicles in vitro
- Published in:
- Cell Biology International, 2006, v. 30, n. 12, p. 999, doi. 10.1016/j.cellbi.2006.07.007
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- Article
Eruptive pruritic papular porokeratosis.
- Published in:
- 2021
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- Publication type:
- Case Study
Three novel ATP2C1 mutations in Chinese patients with Hailey-Hailey disease.
- Published in:
- 2019
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- Publication type:
- Letter to the Editor
Linear cutaneous lupus erythematosus/discoid lupus erythematosus in an adult.
- Published in:
- Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2017, v. 34, n. 2, p. 177, doi. 10.5114/ada.2017.67086
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- Article
Severe Darier's disease patient with mutation of ATP2A2.
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- Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2014, v. 31, n. 5, p. 338, doi. 10.5114/pdia.2014.44030
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- Publication type:
- Article
Patchy alopecia areata sparing gray hairs: a case series.
- Published in:
- Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2014, v. 31, n. 2, p. 113, doi. 10.5114/pdia.2014.40956
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- Publication type:
- Article
A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling.
- Published in:
- 2015
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- Publication type:
- Case Study
Successful Treatment of Eczema-Like Mucormycosis in a Child by Combination of Intravenous Drip and Percutaneous Injection Amphotericin B.
- Published in:
- 2019
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- Publication type:
- Case Study
Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH).
- Published in:
- Human Mutation, 2004, v. 23, n. 6, p. 629, doi. 10.1002/humu.9246
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- Article
Four‐color halo congenital nevus.
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- Journal of Cosmetic Dermatology, 2021, v. 20, n. 11, p. 3712, doi. 10.1111/jocd.14056
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- Publication type:
- Article
Two novel nicastrin mutations in Chinese families with acne inversa.
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- Journal of Dermatology, 2020, v. 47, n. 12, p. e449, doi. 10.1111/1346-8138.15575
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- Publication type:
- Article
Two new mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.
- Published in:
- Archives of Dermatological Research, 2010, v. 302, n. 6, p. 477, doi. 10.1007/s00403-010-1037-4
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- Publication type:
- Article
One novel homozygous mutation of SLC39A4 gene in a Chinese patient with acrodermatitis enteropathica.
- Published in:
- Archives of Dermatological Research, 2010, v. 302, n. 4, p. 315, doi. 10.1007/s00403-010-1047-2
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- Publication type:
- Article