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Research 31–60 of 1000+
- Accelerated Endothelial to Mesenchymal Transition Increased Fibrosis via Deleting Notch Signaling in Wound Vasculature
- Restoration of hair follicle inductive properties by depletion of senescent cells
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Age-induced hair greying - the multiple effects of oxidative stress
- Molecular basis of androgen insensitivity
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- 371 Hair follicles are critical modulators of skin barrier function
- Long‐term culture of skin biopsies: maintenance of fibroblast production and competency of reprogramming
- Transplantation immunology: Solid organ and bone marrow
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Principles of Hair Cycle Control
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- A role of placental growth factor in hair growth
- Retinoic acid and dimethyl sulfoxide promote efficient delivery of transgenes to mouse skin by topically transdermal penetration
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- A mouse with bad hair and poor taste
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Gpr54 deletion accelerates hair cycle and hair regeneration
- 604 DNA dioxygenases TET regulate keratin gene expression and enhancer networks within lineage-specific gene loci during epidermal and hair follicle-specific keratinocyte differentiation
- Deletion of an enhancer in FGF5 is associated with ectopic expression in goat hair follicles and the cashmere growth phenotype
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- MOF-mediated Histone H4 Lysine 16 Acetylation Governs Mitochondrial and Ciliary Functions By Controlling Gene Promoters
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Nelfb promotes dermal white adipose tissue formation through RNA Polymerase II mediated adipogenic gene regulation