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Research 421–450 of 1000+
- Telogen Effluvium
- Gene expression profiling analysis reveals fur development in rex rabbits (<i>Oryctolagus cuniculus</i>)
- Editorial: Stem cell exhaustion in aging
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Physiological Regeneration of Skin Appendages and Implications for Regenerative Medicine
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Thyroid hormone action in epidermal development and homeostasis and its implications in the pathophysiology of the skin
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Pathological sequelae of long-haul COVID
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Tissue Regeneration, Stem Cells, and Wound Healing
- Taurine, a non-proteinous essential amino acid for human body systems: an overview
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Defining the impact of β-catenin/Tcf transactivation on epithelial stem cells
- Stem cells supporting other stem cells
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response