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Research 241–270 of 1000+
- Neurobiology, Stem Cell Biology, and Immunology: An Emerging Triad for Understanding Tissue Homeostasis and Repair
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Generalised Glucocorticoid Resistance
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis
- Inherited Epidermolysis Bullosa: A Clinical Case
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Beyond Expectations
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- FGF5 is a crucial regulator of hair length in humans
- The keratins and their disorders