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Research 331–360 of 1000+
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- 129 Genetic transformation of keratoacanthoma-type cutaneous squamous cell carcinoma following intralesional chemotherapy
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Interleukins gene polymorphism in alopecia areata patients: a systematic review
- Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- 0036 IL-27 generates immunosuppressive CD4 T cells and and prevents the development of alopecia areata
- Long- COVID and general health status in hospitalized COVID-19 survivors
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Comparative spatial transcriptomics of hair follicle-T cell interactions in mouse, dog and human reveals conserved drivers of primary cicatricial alopecia
- 498 A Multi-Omics Approach to create a Human Hair Atlas for healthy and AGA models
- Support for dermatological research in Sub‐Saharan Africa: insights from African hair and skin research programs
- Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- In silico analysis of imprinted gene expression in the mouse skin
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- A mouse with bad hair and poor taste
- Loss of Stem Cells Correlates with Premature Aging in Animal Study, Penn Researchers Find
- Next Generation Therapeutics for Androgenetic Alopecia
- 921 Generation of a new rodent model of scleroderma