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Research 601–630 of 1000+
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Influence of <i>FHIT</i> on benzo[ <i>a</i> ]pyrene-induced tumors and alopecia in mice: Chemoprevention by budesonide and <i>N</i> -acetylcysteine
- Changes of serum trace elements level in patients with alopecia areata: A meta‐analysis
- Serum vitamin D3 level in patients with female pattern hair loss
- Alpha tocopherol-Nanocellulose loaded alginate membranes and Pluronic hydrogels for diabetic wound healing
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Factors associated with anti-SARS-CoV-2 IgG antibody production in patients convalescing from COVID-19
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Hair Minerals and Metabolic Health in Belgian Elementary School Girls
- Androgens stimulate specific aspects of maternal nest-building and reduce food intake in rabbits
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- High‐frequency (22‐MHz) ultrasound for assessing the depth of basal cell carcinoma invasion
- The Inhibition Activity of Tannin on the Formation of Mono-Species and Polymicrobial Biofilm Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans
- Topical minoxidil for extended areate alopecia
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- A second <i>KRT</i>71 allele in curly coated dogs
- Economic Burden and Healthcare Resource Use of Alopecia Areata in an Insured Population in the USA
- The anxiolytic-like effects of estazolam on a PTSD animal model
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Scalp involvement in pemphigus: a prognostic marker
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Sulphate conjugation of minoxidil in rat skin
- Serum Zinc Levels in Women with Polycystic Ovarian Syndrome are Lower as Compared to Those without Polycystic Ovarian Syndrome: A Cohort Study
- Influence of Chemical Straightening on the Stability of Drugs of Abuse in Hair
- Follicle trauma and the role of the dissecting microscope in hair transplantation. A Multicenter Study