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Research 961–990 of 1000+
- 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
- The hair shaft: normality, abnormality, and genetics
- Eyebrow restoration: the approach, considerations, and technique in follicular unit transplantation
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Proposed mechanisms of low-level light therapy in the treatment of androgenetic alopecia
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- The clinical spectrum of parathyroid disease
- Proprietary Herbal Extract Downregulates the Gene Expression of Il-1 and #945; in HaCaT Cells: Possible Implications Against Nonscarring Alopecia
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Skin eruptions specific to pregnancy: an overview
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Diagnosis of an indistinct Leydig cell tumor by positron emission tomography-computed tomography
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Low-level light therapy (LLLT) for cosmetics and dermatology
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Expression of lipid-protein gene PLP2 in Liaoning cashmere goat
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- The urine as a diagnostic key for a homozygous EGFR mutation
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Diversity of Adult Stem Cell Niches in the Dermal Compartment of Skin