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Research 121–150 of 1000+
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Connecting corporations and communities: Towards a theory of social inclusive open innovation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Toxicity studies of iron-containing ayurvedic drug Kasisa Bhasma
- Necrosulfonamide promotes hair growth and ameliorates DHT-induced hair growth inhibition
- Uji Fitokimia dan Stabilitas Fisik Sediaan Hair Tonic Ekstrak Jeruk Nipis (Citrus aurantifolia)
- Regulation of stem cell function by protein ubiquitylation
- Polycystic ovary syndrome and its management: In view of oxidative stress
- Hydroxytyrosol Alleviates Acute Liver Injury by Inhibiting the TNF-α/PI3K/AKT Signaling Pathway via Targeting TNF-α Signaling
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Carbon, nitrogen, and sulfur elemental and isotopic variations in mouse hair and bone collagen during short-term graded calorie restriction
- CuCS/Cur composite wound dressings promote neuralized skin regeneration by rebuilding the nerve cell "factory" in deep skin burns
- 93 Setting Up an Office and the Surgical Suite
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Unlocking the Power of Light on the Skin: A Comprehensive Review on Photobiomodulation
- Molecular signaling in feather morphogenesis
- Nanocarriers as Active Ingredients Enhancers in the Cosmetic Industry—The European and North America Regulation Challenges
- The Localization of Label-Retaining Cells in Mouse Nails
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Evaluating the Metabolomic Profile and Anti-Pathogenic Properties of Cannabis Species
- Leveraging deep neural networks to uncover unprecedented levels of precision in the diagnosis of hair and scalp disorders
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Prediction of cell states and key transcription factors of the human cornea through integrated single-cell omics analyses
- Spherical Skin Model: Stratified Co‐Culture of Fibroblasts and Keratinocytes on Spherical Beads Toward Compound Screening
- Innovative Teaching Strategies for Medical Students: Encouraging Reflection on Patient Experiences Through Creative Methods and Meaningful Connections