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Research 121–150 of 1000+
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Alopecia induced by lopinavir plus ritonavir therapy in an HIV patient.
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- New and Consolidated Therapeutic Options for Pubertal Induction in Hypogonadism: In-depth Review of the Literature
- A Comprehensive Review of Acne Vulgaris
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Oral Lichen Planus
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Physico-chemical properties of modern cosmetics for styling and their effect on hair structure
- Immunological challenges associated with artificial skin grafts: available solutions and stem cells in future design of synthetic skin
- Polysaccharides from Traditional Chinese Medicines: Extraction, Purification, Modification, and Biological Activity
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- The JAK/STAT signaling pathway: from bench to clinic
- Tannic acid-functionalized 3D porous nanofiber sponge for antibiotic-free wound healing with enhanced hemostasis, antibacterial, and antioxidant properties
- Design, Synthesis and Evaluation of N13-Substituted Evodiamine Derivatives against Human Cancer Cell Lines
- A newborn presenting with congenital blistering
- Hypertension's 3 Dilemmas and 3 Solutions: Pharmacology of the Kidney in Hypertension
- Recent Progress in Health Benefits of Hederagenin and Its Glycosides
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Exploring murE protein inhibitors of Tropheryma whipplei through pharmacoinformatic approaches incorporating solubility-enhancing formulation insights
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation