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Research 721–750 of 1000+
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Genetically separable determinants of hair keratin gene expression
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Skin Microbiome Shifts in Various Dermatological Conditions
- Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Patologías dermatológicas de origen nutricional en los pequeños animales: una revisión
- A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Exploring the Complexities of Atopic Dermatitis: Pathophysiological Mechanisms and Therapeutic Approaches
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- The study of the altering of cytokines and growth factors secreted by cultured balding dermal papilla cells
- Aging in the sebaceous gland
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Bifidobacterium Is Enriched in Gut Microbiome of Kashmiri Women with Polycystic Ovary Syndrome
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature
- Uncovering novel biomarkers and drug targets for androgenetic alopecia via metabolite regulation and multi-tissue validation
- Ehlers-Danlos syndrome: From bedside to bench