Page last updated: 2024-08-23

acitretin and Genetic Predisposition

acitretin has been researched along with Genetic Predisposition in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (20.00)29.6817
2010's7 (70.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Chen, W; He, Y; Kuang, Y; Zhou, X; Zhu, W1
Boldrini, R; Carnevale, C; Castiglia, D; Diociaiuti, A; El Hachem, M; Giancristoforo, S; Proto, V; Zambruno, G1
Batilando, MJ; Koh, MJA; Loo, BKG; Tan, EC1
Chen, W; Chen, X; Wu, L; Zhu, W1
Cao, C; Hai, T; Jia, Q; Lam, SM; Li, Y; Liu, Z; Meng, A; Qin, G; Shui, G; Song, R; Wang, X; Wang, Y; Wei, H; Yao, J; Zhang, H; Zhang, Y; Zhao, J; Zheng, Q; Zhou, Q1
Cheng, R; Guo, Y; Huang, P; Li, M; Liang, J; Lu, Z; Wang, Y; Yan, M; Yao, Z1
O'Rielly, DD; Rahman, P1
Barara, M; Chander, R; Garg, T; Jabeen, M; Jain, M; Mittal, K; Puri, V1
Allen, MH; Barker, JN; Burden, AD; Campalani, E; Crook, MA; Fairhurst, D; Griffiths, CE; Mendonca, CO; Smith, CH; Young, HS1
Bagci, Y; Erdogan, S; Erkek, E; Kurtipek, GS; Ozdemir, S; Ozoguz, P; Tuncez, F1

Reviews

1 review(s) available for acitretin and Genetic Predisposition

ArticleYear
Pharmacogenetics of psoriasis.
    Pharmacogenomics, 2011, Volume: 12, Issue:1

    Topics: Acitretin; Adrenal Cortex Hormones; Antibodies, Monoclonal; Cyclosporine; Genetic Predisposition to Disease; Humans; Methotrexate; Pharmacogenetics; Precision Medicine; Psoriasis

2011

Other Studies

9 other study(ies) available for acitretin and Genetic Predisposition

ArticleYear
    Frontiers in bioscience (Landmark edition), 2022, 09-28, Volume: 27, Issue:9

    Topics: Acitretin; Alleles; Genetic Predisposition to Disease; HLA-C Antigens; HLA-DQ alpha-Chains; HLA-DQ beta-Chains; Humans; Psoriasis

2022
Lipoid Proteinosis: A Previously Unrecognized Mutation and Therapeutic Response to Acitretin.
    Acta dermato-venereologica, 2017, Nov-15, Volume: 97, Issue:10

    Topics: Acitretin; Administration, Oral; Adolescent; DNA Mutational Analysis; Extracellular Matrix Proteins; Genetic Predisposition to Disease; Humans; Keratolytic Agents; Lipoid Proteinosis of Urbach and Wiethe; Male; Mutation; Phenotype; Tomography, X-Ray Computed; Treatment Outcome

2017
Compound heterozygous mutations with novel missense
    BMJ case reports, 2018, Jan-03, Volume: 2018

    Topics: Acitretin; ATP-Binding Cassette Transporters; Female; Genetic Predisposition to Disease; Genotype; Humans; Ichthyosis, Lamellar; Infant, Newborn; Keratolytic Agents; Mutation; Mutation, Missense; Polymorphism, Single Nucleotide; Prenatal Diagnosis; Sequence Deletion; Treatment Outcome

2018
The polymorphisms of growth factor genes (VEGFA & EGF) were associated with response to acitretin in psoriasis.
    Personalized medicine, 2018, 05-01, Volume: 15, Issue:3

    Topics: Acitretin; Adult; Calcitriol; China; Drug Administration Schedule; Epidermal Growth Factor; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Psoriasis; Vascular Endothelial Growth Factor A

2018
A harlequin ichthyosis pig model with a novel ABCA12 mutation can be rescued by acitretin treatment.
    Journal of molecular cell biology, 2019, 12-19, Volume: 11, Issue:12

    Topics: Acitretin; Alleles; Animals; ATP-Binding Cassette Transporters; Biopsy; Cell Differentiation; Chromosome Mapping; Disease Management; Disease Models, Animal; Epidermal Cells; Gene Expression; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Ichthyosis, Lamellar; Immunohistochemistry; Introns; Lipid Metabolism; Mutation; Phenotype; Skin; Swine

2019
Clinical profiles of pediatric patients with GPP alone and with different IL36RN genotypes.
    Journal of dermatological science, 2017, Volume: 85, Issue:3

    Topics: Acitretin; Adolescent; Asian People; Child; Child, Preschool; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Genotype; Heterozygote; Homozygote; Humans; Interleukins; Keratolytic Agents; Male; Mutation; Prospective Studies; Psoriasis; Recurrence; Retrospective Studies; Suppuration; Withholding Treatment

2017
Amyloidosis cutis dyschromica: a rare pigmentary disorder.
    Journal of cutaneous pathology, 2011, Volume: 38, Issue:10

    Topics: Acitretin; Amyloidosis; Family; Female; Genetic Predisposition to Disease; Humans; Keratolytic Agents; Pigmentation Disorders; Skin Diseases, Vesiculobullous; Sunscreening Agents; Young Adult

2011
Apolipoprotein E gene polymorphisms are associated with psoriasis but do not determine disease response to acitretin.
    The British journal of dermatology, 2006, Volume: 154, Issue:2

    Topics: Acitretin; Adolescent; Adult; Aged; Aged, 80 and over; Apolipoprotein E4; Apolipoproteins E; Child; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Hypertriglyceridemia; Keratolytic Agents; Male; Middle Aged; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Psoriasis; Sequence Analysis, DNA; Treatment Outcome

2006
Type I hereditary punctate keratoderma associated with widespread lentigo simplex and successfully treated with low-dose oral acitretin.
    Archives of dermatology, 2006, Volume: 142, Issue:8

    Topics: Acitretin; Administration, Oral; Aged; Diagnosis, Differential; Female; Genetic Predisposition to Disease; Humans; Keratoderma, Palmoplantar; Keratolytic Agents; Lentigo

2006