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Research 391–420 of 1000+
- Biology of melanocytes in mammals
- Latanoprost-Loaded Nanotransfersomes Designed for Scalp Administration Enhance Keratinocytes Proliferation
- The Spectrum of Skin Disease Among Indian Children
- Infertility: Evaluation and Initial Management
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Methotrexate in dermatology
- Wnt signaling: the good and the bad
- Androgenetic Alopecia: Therapy Update
- The clinical spectrum of parathyroid disease
- Oral vitamin A as an adjunct treatment for canine sebaceous adenitis
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Alopecia areata
- Recognition and management of <i>Staphylococcus aureus</i> toxin‐mediated disease
- Aging of hair
- No metabolic impact of surgical normalization of hyperandrogenism in postmenopausal women with ovarian androgen-secreting tumours
- Optimizing skin disease diagnosis: harnessing online community data with contrastive learning and clustering techniques
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Hair Amino Acids: Normal Values and Results in Metabolic Errors
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Membranous nephropathy and lupus-like syndrome after hematopoietic cell transplantation: a case report
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Answer
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Safety assessment of cyclin-dependent kinase 4/6 inhibitors and comparison of time to adverse events