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Research 511–540 of 1000+
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Congenital atrichia and hypotrichosis
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- Hyperadrenocorticism in Ferrets
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Progeroide Syndrome
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Neuroactive Steroids and Ethanol Exposure: Relevance to Ethanol Sensitivity and Alcohol Use Disorders Risk
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Evolutionary Divergence of Fibroblast Growth Factors Across Species: Insight into Functional Diversification
- Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Genetic Defects of Female Sexual Differentiation
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Modelling androgen synthesis and action during human sexual differentiation
- Syndromes of Severe Insulin Resistance (SSIRs)
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Control of hair growth and follicle size by VEGF-mediated angiogenesis