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Research 61–90 of 1000+
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Local circadian clock gates cell cycle progression of transient amplifying cells during regenerative hair cycling
- Clock genes, hair growth and aging
- Diagnostic Value of VDR in Bone Metastasis and Prognosis of Patients with Breast Cancer and Expression Correlation between Vitamin D Receptor and Hairless Protein
- Hair & Cutaneous Development
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- DKK4 as a novel candidate marker for Zhexi Angora rabbit wool quality
- Boron deficiency responses in maize (<i>Zea mays</i> L.) roots
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Hormone receptor positive, HER2 negative metastatic breast cancer: Impact of CDK4/6 inhibitors on the current treatment paradigm
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Le gène<i>hairless</i>de la souris
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- A missense mutation in Lama3 causes androgen alopecia
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Gab1 and Mapk Signaling Are Essential in the Hair Cycle and Hair Follicle Stem Cell Quiescence
- Insertional mutation of the hairless locus on mouse Chromosome 14