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DNA methylation-based subclassification of psoriasis in the Chinese Han population.
- Published in:
- Frontiers of Medicine, 2018, v. 12, n. 6, p. 717, doi. 10.1007/s11684-017-0588-6
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- Article
Noninvasive Analysis Using Data-Independent Acquisition Mass Spectrometry: New Epidermal Proteins That Reveal Sex Differences in the Aging Process.
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- Oxidative Medicine & Cellular Longevity, 2021, p. 1, doi. 10.1155/2021/8849328
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- Article
DNA methylation age is not affected in psoriatic skin tissue.
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- Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0584-y
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- Article
Epigenome-wide association data implicates DNA methylation-mediated genetic risk in psoriasis.
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- Clinical Epigenetics, 2016, v. 8, p. 1, doi. 10.1186/s13148-016-0297-z
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- Article
Genome‐wide meta‐analyses identify five new risk loci for nonsyndromic orofacial clefts in the Chinese Han population.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 10, p. 1, doi. 10.1002/mgg3.2226
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- Article
Gene interaction analysis of psoriasis in Chinese Han population.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 5, p. 1, doi. 10.1002/mgg3.1858
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- Article
A Novel Mutation of CYLD Gene in a Chinese Family with Multiple Familial Trichoepithelioma.
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- Australasian Journal of Dermatology, 2014, v. 55, n. 3, p. 232, doi. 10.1111/ajd.12210
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- Article
Fine Mapping Analysis of the MHC Region to Identify Variants Associated With Chinese Vitiligo and SLE and Association Across These Diseases.
- Published in:
- Frontiers in Immunology, 2022, v. 12, p. 1, doi. 10.3389/fimmu.2021.758652
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- Article
A commentary on exome sequencing identifies a de novo mutation in HDAC8 associated with Cornelia de Lange syndrome.
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- Journal of Human Genetics, 2014, v. 59, n. 9, p. 479, doi. 10.1038/jhg.2014.68
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- Article
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy.
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- Nature Genetics, 2011, v. 43, n. 12, p. 1247, doi. 10.1038/ng.973
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- Article
Four genetic variants interact to confer susceptibility to atopic dermatitis in Chinese Han population.
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- Molecular Genetics & Genomics, 2015, v. 290, n. 4, p. 1493, doi. 10.1007/s00438-015-1014-x
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- Article
Diverse phenotype of Brooke–Spiegler syndrome associated with a nonsense mutation in the CYLD tumor suppressor gene.
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- Experimental Dermatology, 2006, v. 15, n. 12, p. 966, doi. 10.1111/j.1600-0625.2006.00501.x
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- Article
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
- Published in:
- Scientific Reports, 2017, p. 44155, doi. 10.1038/srep44155
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- Article
Filaggrin Gene Mutation c.3321delA Is Associated with Various Clinical Features of Atopic Dermatitis in the Chinese Han Population.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098235
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- Article
Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071771
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- Article
An Effort to Use Human-Based Exome Capture Methods to Analyze Chimpanzee and Macaque Exomes.
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- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040637
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- Article
HLA-A*01:01 in MHC is associated with psoriatic arthritis in Chinese Han population.
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- Archives of Dermatological Research, 2019, v. 311, n. 4, p. 277, doi. 10.1007/s00403-019-01902-3
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- Article
Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci.
- Published in:
- Frontiers in Genetics, 2016, p. 1, doi. 10.3389/fgene.2016.00003
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- Article
Correlation between double‐stranded DNA and acute urticaria.
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- International Journal of Dermatology, 2024, v. 63, n. 8, p. e140, doi. 10.1111/ijd.17086
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- Article
A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population.
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- Journal of the European Academy of Dermatology & Venereology, 2012, v. 26, n. 9, p. 1137, doi. 10.1111/j.1468-3083.2011.04259.x
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- Article
Cutaneous Calcium/Calmodulin‐Dependent Protein Kinase II‐γ–Positive Sympathetic Nerves Secreting Norepinephrine Dictate Psoriasis.
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- Advanced Science, 2024, v. 11, n. 23, p. 1, doi. 10.1002/advs.202306772
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- Article
Cutaneous Calcium/Calmodulin‐Dependent Protein Kinase II‐γ–Positive Sympathetic Nerves Secreting Norepinephrine Dictate Psoriasis (Adv. Sci. 23/2024).
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- Advanced Science, 2024, v. 11, n. 23, p. 1, doi. 10.1002/advs.202470137
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- Article
Platelet-derived Growth Factor Receptor Alpha Gene Mutations in Vitiligo Vulgaris.
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- Acta Dermato-Venereologica, 2010, v. 90, n. 2, p. 131, doi. 10.2340/00015555-0820
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- Article
Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus.
- Published in:
- Arthritis Research & Therapy, 2015, v. 17, n. 1, p. 1, doi. 10.1186/s13075-015-0577-6
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- Article
Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.
- Published in:
- Nature Communications, 2015, v. 6, n. 4, p. 6793, doi. 10.1038/ncomms7793
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- Publication type:
- Article
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.
- Published in:
- Nature Communications, 2015, v. 6, n. 4, p. 6916, doi. 10.1038/ncomms7916
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- Article
Knockdown of myosin VI by lentivirus-mediated short hairpin RNA suppresses proliferation of melanoma.
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- Molecular Medicine Reports, 2015, v. 12, n. 5, p. 6801, doi. 10.3892/mmr.2015.4261
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- Article
A Genetic Variant rs1020760at NFKB1 is Associated with Clinical Features of Psoriasis Vulgaris in a Han Chinese Population.
- Published in:
- Annals of Human Genetics, 2016, v. 80, n. 4, p. 197, doi. 10.1111/ahg.12156
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- Article
Six Mutations in AAGAB Confirm Its Pathogenic Role in Chinese Punctate Palmoplantar Keratoderma Patients.
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- Journal of Investigative Dermatology, 2013, v. 133, n. 11, p. 2631, doi. 10.1038/jid.2013.198
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- Article
Evidence for Two Susceptibility Loci on Chromosomes 22q12 and 6p21–p22 in Chinese Generalized Vitiligo Families.
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- Journal of Investigative Dermatology, 2007, v. 127, n. 11, p. 2552, doi. 10.1038/sj.jid.5700904
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- Article
A method mediated AAVS1 recombination with Rep mRNA and homologous arms.
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- Acta Biochimica et Biophysica Sinica, 2012, v. 44, n. 12, p. 1015, doi. 10.1093/abbs/gms076
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- Article
Mutational analysis of epidermal and hyperproliferative type I keratins in mild and moderate psoriasis vulgaris patients: a possible role in the pathogenesis of psoriasis along with disease severity.
- Published in:
- Human Genomics, 2018, v. 12, n. 1, p. N.PAG, doi. 10.1186/s40246-018-0158-2
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- Article
Genome‐wide association study of 7661 Chinese Han individuals and fine‐mapping major histocompatibility complex identifies HLA‐DRB1 as associated with IgA vasculitis.
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- Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 6, p. 1, doi. 10.1002/jcla.24457
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- Article
Novel susceptibility loci for A(H7N9) infection identified by next generation sequencing and functional analysis.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68675-y
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- Article
Low-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese men.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 19, p. 5628, doi. 10.1093/hmg/ddv257
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- Article
Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 1, p. 274, doi. 10.1093/hmg/ddu429
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- Article
Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 2, p. 524, doi. 10.1093/hmg/ddt424
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- Article
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 11, p. 2325, doi. 10.1093/hmg/ddt066
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- Article
Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01014-w
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- Article
Rs4948496 within ARID5B gene is associated with clinical features of systemic lupus erythematosus in the Chinese Han population.
- Published in:
- Journal of Dermatology, 2015, v. 42, n. 6, p. 608, doi. 10.1111/1346-8138.12841
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- Article
MST1 modulates Th17 activation in psoriasis via regulating TLR4-NF-κB pathway.
- Published in:
- Human Cell, 2021, v. 34, n. 1, p. 28, doi. 10.1007/s13577-020-00423-w
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- Article
Correction to: Rare mutations in NLRP3 and NLRP12 associated with familial cold autoinflammatory syndrome: two Chinese pedigrees.
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- 2022
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- Correction Notice
Rare mutations in NLRP3 and NLRP12 associated with familial cold autoinflammatory syndrome: two Chinese pedigrees.
- Published in:
- Clinical Rheumatology, 2022, v. 41, n. 11, p. 3461, doi. 10.1007/s10067-022-06292-y
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- Publication type:
- Article
Knockdown of asparagine synthetase by RNAi suppresses cell growth in human melanoma cells and epidermoid carcinoma cells.
- Published in:
- Biotechnology & Applied Biochemistry, 2016, v. 63, n. 3, p. 328, doi. 10.1002/bab.1383
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- Article
Knockdown of EIF3D suppresses proliferation of human melanoma cells through G2/M phase arrest.
- Published in:
- Biotechnology & Applied Biochemistry, 2015, v. 62, n. 5, p. 615, doi. 10.1002/bab.1305
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- Article
Association of the Polymorphism rs13259960 in SLEAR With Predisposition to Systemic Lupus Erythematosus.
- Published in:
- Arthritis & Rheumatology, 2020, v. 72, n. 6, p. 985, doi. 10.1002/art.41200
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- Publication type:
- Article
Gene-Based Meta-Analysis of Genome-Wide Association Study Data Identifies Independent Single-Nucleotide Polymorphisms in ANXA6 as Being Associated With Systemic Lupus Erythematosus in Asian Populations.
- Published in:
- Arthritis & Rheumatology, 2015, v. 67, n. 11, p. 2966, doi. 10.1002/art.39275
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- Article
Fine-Mapping of the Major Histocompatibility Complex Region Linked to Leprosy in Northern China.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.768259
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- Article
Author Correction: Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.
- Published in:
- Nature Communications, 2018, v. 9, p. 16186, doi. 10.1038/ncomms16186
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- Publication type:
- Article
Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000523
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- Article