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Research 331–360 of 1000+
- Bone Metabolism in Patients with Hidradenitis Suppurativa: A Case-control Study
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Immunohistochemical, pharmacovigilance, and omics analyses reveal the involvement of ATP-sensitive K+ channel subunits in cancers: role in drug–disease interactions
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Targeting the Warburg Effect in Anaplastic Thyroid Carcinoma: Metabolic Vulnerabilities and Therapeutic Opportunities
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Computational Drug Repositioning in Cardiorenal Disease: Opportunities, Challenges, and Approaches
- Understanding Type 3 Innate Lymphoid Cells and Crosstalk with the Microbiota: A Skin Connection
- Proteins in Scalp Hair of Preschool Children
- E-Poster
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Ectopic olfactory receptors in human: New therapeutic possibilities
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Expression of Peroxisome Proliferator Activated Receptors (PPARs) in Human Hair Follicles and PPARα Involvement in Hair Growth
- Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol