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Research 511–540 of 1000+
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Birt–Hogg–Dubé syndrome
- Sperm extraction in nonmosaic Klinefelter syndrome patients: A case series and literature review of sperm extraction in Klinefelter syndrome patients
- A malignant proliferating trichilemmal cyst arising on the elbow of a man: A case report and review of the literature
- LB943 Tofacitinib treatment of inflammatory skin conditions in patients with Down Syndrome
- 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
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- The Pharmacokinetics of Topical Finasteride 0.25% Spray in Chinese Adult Male Volunteers with Androgenic Alopecia: A Phase I Study
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Netherton Syndrome
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Abstract C4: Sp2: A regulator of stem cell differentiation and tumorigenesis
- Uncomplicated differentiation of stem cells into bipolar neurons and myelinating glia
- Cellular and Immunological Aspects of Basel Cell Carcinoma
- Cellular and Immunological Aspects of Basel Cell Carcinoma
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- Evaluating the Therapeutic Potential of Ritlecitinib for the Treatment of Alopecia Areata
- Characterization and expression analysis of KAP7.1, KAP8.2 gene in Liaoning new-breeding cashmere goat hair follicle
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- A Comprehensive Review on Skin Pigmentation-Types, Causes, and Treatment
- The fiber diameter traits of Tibetan cashmere goats are governed by the inherent differences in stress, hypoxic, and metabolic adaptations: an integrative study of proteome and transcriptome
- Diversity of Trichocyte Keratins and Keratin Associated Proteins
- Improving the treatment of bacterial infections caused by multidrug-resistant bacteria through drug repositioning
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- New hyaluronan-based biomatrix for 3-D follicle culture yields functionally competent oocytes
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat