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Research 121–150 of 1000+
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- The semiotics of breast cancer: Signs, symptoms, and sales
- Guava (Psidium guajava L.) Leaf Bioactives: From Phytochemical Characterization to Therapeutic and Technological Applications
- Guava (Psidium guajava L.) Leaf Bioactives: From Phytochemical Characterization to Therapeutic and Technological Applications
- Air Wedge Interferometry for Microscopic Thickness Measurement of Human Hair
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Clinical features of non‐classical 21‐hydroxylase deficiency after normal newborn mass screening
- Comments concerning the real risk of sexual adverse events secondary to the use of 5-ARIs
- Acknowledging the Clinical Heterogeneity of Lupus Erythematosus
- Trichothiodystrophy in a child with occult learning disorder
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Engineering Cell Surfaces with Polyelectrolyte Materials for Translational Applications
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- National scientific medical meeting 1996 abstracts
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Growth and viability of Liaoning Cashmere goat hair follicles during the annual hair follicle cycle
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Tissue engineering; strategies, tissues, and biomaterials
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- 832 Variability in secretion of growth factors by platelets is intrinsic to alopecia patients undergoing platelet-rich plasma therapy
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products
- Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair