Search
for
Sort by
Research 151–180 of 1000+
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- 1418 Characterization of ectomesenchyme as an origin of epidermal stem cells
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Selected Abstracts
- Developmental origin of polycystic ovary syndrome - a hypothesis
- Nonviral in Situ Green Fluorescent Protein Labeling and Culture of Primary, Adult Human Hair Follicle Epithelial Progenitor Cells
- Human platelet lysate versus minoxidil stimulates hair growth by activating anagen promoting signaling pathways
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Two females with hair loss
- This Month in the Journal
- Finding bald spots on chromosome 20p11
- Congenital atrichia with papular lesions
- ダブルストロボレンジファインダの開発(特別講演)(画像センシングおよび一般)
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors
- A mouse with bad hair and poor taste
- News in brief
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS