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Research 661–690 of 1000+
- The Basic Science of Hair Biology
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Reprogramming of Human Hair Follicle Dermal Papilla Cells into Induced Pluripotent Stem Cells
- Stem cells and aberrant signaling of molecular systems in skin aging
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Alopecia Areata
- Cicatricial alopecia
- Dermatological Manifestations of Stress in Normal and Psychiatric Populations
- Alopecia.
- Induction of Skin-Derived Precursor Cells from Human Induced Pluripotent Stem Cells
- Defining the identity of mouse embryonic dermal fibroblasts
- Alopecia in Epidermolysis Bullosa
- Clinical Approach to the Patient With Alopecia
- Evaluation of hair loss
- Epimorphic regeneration in mice is p53-independent
- Unruly hair
- Characterization of <i>BMP</i>2 gene expression in embryonic and adult Inner Mongolia Cashmere goat (<i>Capra hircus</i>) hair follicles
- Bioactive Molecules for Skin Repair and Regeneration: Progress and Perspectives
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Histopathological insights into hair loss in Cronkhite-Canada syndrome: Diffuse anagen-telogen conversion precedes clinical hair loss progression
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Dental derived stem cell conditioned media for hair growth stimulation
- Regeneration of rete ridges in Lanyu pig ( <i>Sus scrofa</i> ): Insights for human skin wound healing
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Short anagen syndrome: Case series and literature review
- Loose anagen hair syndrome in children of Upper Egypt
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- Dermatologic manifestations of endocrine disorders
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation