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Research 961–990 of 1000+
- Premature Graying, Balding, and Low Bone Mineral Density in Older Women and Men
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Epigenetic regulation and factors that influence the effect of iPSCs-derived neural stem/progenitor cells (NS/PCs) in the treatment of spinal cord injury
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Auditory Threshold Variability in the SAMP8 Mouse Model of Age-Related Hearing Loss: Functional Loss and Phenotypic Change Precede Outer Hair Cell Loss
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Pili annulati with fragility: Electron microscopic findings of a case
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- Male Androgenetic Alopecia
- Hair shaft disorders in children – An update
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Male fertility and skin diseases
- Comparison of pemetrexed and docetaxel as salvage chemotherapy for the treatment for nonsmall-cell lung cancer after the failure of epidermal growth factor receptor-tyrosine kinase inhibitors
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A rare case of woolly hair with unusual associations
- Activation of mitochondrial aldehyde dehydrogenase 2 promotes hair growth in human hair follicles
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Molecular Basis of Androgenetic Alopecia
- Electro-optical imaging of F-actin and endoplasmic reticulum in living and fixed plant cells.
- Biological characteristics of age-related changes in C57BL/6 mice sub-strains in the national center for geriatrics and gerontology aging farm
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Sex-limited chromosomes and non-reproductive traits
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin