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Research 361–390 of 1000+
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Dicer- and BSC-dependent miRNAs during murine anagen development
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- The Role of Histone Demethylases in Disease
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Irradiation-induced hair graying in mice: an experimental model to evaluate the effectiveness of interventions targeting oxidative stress, DNA damage prevention, and cellular senescence
- Androgen excess: a hallmark of polycystic ovary syndrome
- Seasonal Gene Expression Profile Responsible for Hair Follicle Development in Angora Goats
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Ageratum Conyzoides L. Extract Inhibits 5α-Reductase Gene Expression and Prostaglandin D2 Release in Human Hair Dermal Papilla Cells and Improves Symptoms of Hair Loss in Otherwise Healthy Males and Females in an Open Label Pilot Study
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Australasian Society for Dermatology Research Meeting, May 2006
- Registrars’ Symposium: Summaries of Papers
- Syndromes of Severe Insulin Resistance (SSIRs)
- Molecular genetics of androgen insensitivity
- Cutaneous signals of immune system disease
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Fibroblast growth factor 5-short (FGF5s) inhibits the activity of FGF5 in primary and secondary hair follicle dermal papilla cells of cashmere goats
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14