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Research 451–480 of 680
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Role of janus kinase inhibitors in the treatment of alopecia areata
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Network pharmacology and molecular docking analysis on potential molecular targets and mechanism of action of BRAF inhibitors for application in wound healing
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Building Models for Keratin Disorders
- Psychological Stress-Induced Pathogenesis of Alopecia Areata: Autoimmune and Apoptotic Pathways
- The incidental pore: Ca<sub>V</sub>1.2 and stem cell activation in quiescent hair follicles
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
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- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Ovarian hormones and adrenal androgens during a woman's life span
- Correction of Tear Trough Deformity Using Autologous Fibroblast Combined with Keratin: New Soft Tissue Filler
- A review of hyperandrogenism state in polycystic ovarian syndrome
- Soft Tissue Augmentation of the Temporal Brow in Browlifting Surgery
- Pharmacogenetics of the Androgen Metabolic Pathway
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation