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Research 721–750 of 1000+
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Assessment of the impact of VDR polymorphisms on selected hormonal, metabolic and mineral balance markers in young women with hyperandrogenism
- In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males”
- Mommy — where do tumors come from?
- Keratin disorders: from gene to therapy
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- FOXN1 deficient nude severe combined immunodeficiency
- The molecular pathogenesis of Trichilemmal carcinoma
- Skin precancer.
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Predicting Human Appearance from DNA for Forensic Investigations
- Copper Deficiency a New Reason of Androgenetic Alopecia?
- Functional analysis of the PIP5K1A gene in Liaoning Cashmere goats: an investigation based on bioinformatics, tissue localization, and biological functions
- Trichilemmal Carcinoma of the Thigh
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Investigations of 13 Genes in Non-Cicatricial Alopecia
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Red Blood Cells Folate Level in Patients with Alopecia Areata