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Research 30 of 1000+
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- TOR tour to auxin
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- GLI2-specific Transcriptional Activation of the Bone Morphogenetic Protein/Activin Antagonist Follistatin in Human Epidermal Cells
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Expression and tissue distribution analysis of vimentin and transthyretin proteins associated with coat colors in sheep (Ovis aries)
- Polarity signaling ensures epidermal homeostasis by coupling cellular mechanics and genomic integrity
- Hairless is a nuclear receptor corepressor essential for skin function
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Overactivated sonic hedgehog signaling aggravates intrauterine adhesion via inhibiting autophagy in endometrial stromal cells
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- YAP1 promotes adipogenesis by regulating the negative feedback mechanism of the Hippo signaling pathway via LATS2
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Hair growth-promoting effect of recombinant human sonic hedgehog proteins
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Targeting the Wnt pathways for therapies
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Biology and Genetics of Hair
- Congenital hair loss disorders: Rare, but not too rare
- Molecular Genetics of Alopecias
- Inherited Disorders of the Hair
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Comparative Proteomics Indicates That Biosynthesis of Pectic Precursors Is Important for Cotton Fiber and Arabidopsis Root Hair Elongation
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders