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Research 451–480 of 1000+
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The Genetics of Human Skin Disease
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Is polycystic ovary syndrome a sexual conflict? A review
- CCN2 modulates hair follicle cycling in mice
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- A curated catalog of canine and equine keratin genes
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Recent discoveries and developments of androgen receptor based therapy for prostate cancer
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Increased dipicolinic acid production with an enhanced <i>spoVF</i> operon in <i>Bacillus subtilis</i> and medium optimization
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- Demethylation of ITGAV accelerates osteogenic differentiation in a blast-induced heterotopic ossification in vitro cell culture model
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Predominant expression of 5 alpha-reductase type 1 in pubic skin from normal subjects and hirsute patients.
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Structural optimization of pep7, a small peptide extracted from epimorphin, for effective induction of hair follicle anagen