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Research 601–630 of 1000+
- Skin tissue engineering
- Global Trends in Research of Androgen Receptor Associated With Breast Cancer From 2011 to 2020: A Scientometric Analysis
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Trichoscopy and Computational Models for Hair and Scalp Disorders: Image Analysis, Quantification, and Clinical Integration
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- Plant elicitor Peptides regulate root hair development in Arabidopsis
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Short Peptides Induce Development of Root Hair Nicotiana tabacum
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Transcriptomes reveal microRNAs and mRNAs in different photoperiods influencing cashmere growth in goat