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Research 121–150 of 1000+
- Human skin color: Origin, variation and significance
- Pigmentary mosaicism: An update
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Serum Ferritin Levels amongst Individuals with Androgenetic Alopecia in Ile-Ife, Nigeria.
- Distinct mechanisms underlie pattern formation in the skin and skin appendages
- Microstructure of Defective Mink Guard Hair
- Polarized microscopy in genetic hair disorders: case series
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Genetic Defects of Female Sexual Differentiation
- Rapid Genetic Analysis of Epithelial-Mesenchymal Signaling During Hair Regeneration
- Female patients complaining about hair loss: documentation of defective scalp hair dynamics with contrast-enhanced phototrichogram
- Biology and Genetics of Hair
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Hair Loss in Children
- Genetic hair and nail disorders
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Trichoscopy in genetic hair shaft abnormalities
- Molecular Genetics of Alopecias
- Advances in Hair Diseases
- Current Genetics in Hair Diseases