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Research 391–420 of 639
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- 54022 Pooled Safety Assessments from the Multinational Phase 3 THRIVE-AA1 and THRIVE-AA2 Trials of Deuruxolitinib in Adult Patients with Moderate to Severe Alopecia Areata
- Coexistence of dermatomyositis and alopecia areata: Insight into pathogenesis
- Corticotropin releasing hormone and the skin
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A subpopulation of itch‐sensing neurons marked by Ret and somatostatin expression
- Does prostaglandin D<sub>2</sub> hold the cure to male pattern baldness?
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- Role of insulin resistance and diet in acne
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- VEGF165 modulates proliferation, adhesion, migration and differentiation of cultured human outer root sheath cells from central hair follicle epithelium through VEGFR-2 activation in vitro
- VEGF upregulates VEGF receptor-2 on human outer root sheath cells and stimulates proliferation through ERK pathway
- Lysophosphatidic acid and signaling in sensory neurons
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Hair Follicle Chemosensation: TRPM5 Signaling Is Required for Anagen Maintenance
- Serum Zinc Levels in Women with Polycystic Ovarian Syndrome are Lower as Compared to Those without Polycystic Ovarian Syndrome: A Cohort Study
- Store-operated calcium channels in skin
- Alopezien und Hypotrichosen im Kindesalter
- Amphiregulin in Fibrotic Diseases and Cancer
- Lipid signaling in keratinocytes: Lipin-1 plays a PArt
- Skin Stearoyl-CoA Desaturase Genes
- 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
- A new START
- Editor's evaluation: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- Immunohistochemical expressions of mGluR5, P2Y2 receptor, PLC-?1, and IP3R-I and -II in Merkel cells in rat sinus hair follicles
- JAK inhibition in the treatment of alopecia areata – a promising new dawn?
- Acute diffuse and total alopecia of the female scalp associated with borrelia-infection
- Sodium Valproate-Induced Hyperpigmentation
- Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome