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Research 751–780 of 802
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Integrated Multi-Omics Analysis Reveals Dysregulated Lipid Metabolism as a Novel Mechanism in Androgenetic Alopecia
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Multi-omics analyses, cell experiments, and network pharmacology tools identified key proteins and candidate drugs for alopecia areata treatment
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- The Role of BMP7 in the Proliferation of Hu Sheep Dermal Papilla Cells Is Influenced by DNA Methylation
- Hair
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Pathogenesis and regenerative therapy in vitiligo and alopecia areata: focus on hair follicle
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- Pharmacogenetics of the Androgen Metabolic Pathway
- Proteome Analysis of Human Hair Shaft
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Hordenine Activated Dermal Papilla Cells and Promoted Hair Regrowth by Activating Wnt Signaling Pathway
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- SRD5A2 and emerging therapies in androgen-driven disorders
- MOESM1 of A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- Association between TLR1 polymorphisms and alopecia areata
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Siberian cats help in solving part of the mystery surrounding golden cats
- Genetics of blond hair
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease
- 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)
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Electrophysiological and Histopathological Effects of Minoxidil on Penicillin-Induced Epilepsy Model in Rats