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Research 151–180 of 1000+
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Review of Promising Off-Label Use of Deucravacitinib
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Pathogenesis and regenerative therapy in vitiligo and alopecia areata: focus on hair follicle
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Effects of Androgen Treatment on Growth in Patients with 5-α-Reductase Type 2 Deficiency
- The role of WNT10B in physiology and disease: A 10-year update
- Subcellular localization of the five members of the human steroid 5α-reductase family
- Premature aging syndromes: From patients to mechanism
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Author response: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Molecular Genetics of Alopecias
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Cyclosporine-Induced Alopecia in Childhood Nephrotic Syndrome – A Case Report
- Spatial variation and associated genes of total hair follicle density in goats
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures