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Research 181–210 of 247
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Incidence Rates of Infections, Malignancies, Thromboembolism, and Cardiovascular Events in an Alopecia Areata Cohort from a US Claims Database
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Keratinic amyloid deposition in canine hair follicle tumors
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Reporting in clinical studies on platelet-rich plasma therapy among all medical specialties: A systematic review of Level I and II studies
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
- Boundary Conditions Cause Different Generic Bifurcation Structures in Turing Systems
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- Social Perception of Male Faces. Individuals, Clusters, Dimensions
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- HAIR DISEASES
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Platelet-Rich Plasma in the Treatment of Androgenetic Alopecia: An Equation with Many Unknowns
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Scalp Dysesthesia
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Extraction and Detection of mRNA from Horsehair
- DRUG‐ASSOCIATED ALOPECIA
- Cyberbabes: (Self-) representation of women and the virtual male gaze
- Rapid Screening of Anticoagulation Compounds for Biological Target-Associated Adverse Effects Using a Deep-Learning Framework in the Management of Atrial Fibrillation
- Hair transparency decoding in Asia: From stylists’ perception to in vitro measurement