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Research 811–840 of 1000+
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- Analysis of histological and microRNA profiles changes in rabbit skin development
- Frontal fibrosing alopecia: a disease fascinating for the researcher, disappointing for the clinician and distressing for the patient
- Dermal EZH2 simultaneously orchestrates dermal differentiation and epidermal proliferation during murine skin development
- Gut microbiota in alopecia areata
- 196 The endocannabinoid tone regulates human sebocyte biology
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Spatial variation and associated genes of total hair follicle density in goats
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- The influence of CD26+ and CD26− fibroblasts on the regeneration of human dermo-epidermal skin substitutes
- Demethylation of ITGAV accelerates osteogenic differentiation in a blast-induced heterotopic ossification in vitro cell culture model
- γδ17 T cell-stromal networks modulate matrix composition and vascularity in foreign body response
- Low Humidity Alters Epidermal Gene Expression in vivo
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1