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Research 331–360 of 1000+
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Diffuse loss of hair with papules
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Adult polycystic ovary syndrome begins in childhood
- Nutrition and Hair
- α3β1-integrin regulates hair follicle but not interfollicular morphogenesis in adult epidermis
- Retrospective evaluation of sex hormones and steroid hormone intermediates in dogs with alopecia
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- From a stem-cell–centered to a niche-centered view: the core role of collagen networks in hair loss and hair follicle miniaturization
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Hair Shaft Dysplasias
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Lifestyle changes and Nutrition in Polycystic Ovarian Disorder: A Holistic Review
- Confocal microscopy and optical coherence tomography of inflammatory skin diseases in hairs and pilosebaceous units: A systematic review
- Effect of calcium supplementation on bone deformity and histopathological findings of skin papules in a pediatric patient with vitamin D–dependent rickets type 2A: a case report
- Cycle pilaire et alopécie X chez le chien
- TONGUE, RED
- Acne
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Disorders of ovulation
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Hair shaft disorders
- Ophthalmologic Comorbidities in Alopecia Areata
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A brief report on PCOS: and its inducing model