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Research 661–690 of 1000+
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Pegylated-interferon-α<sub>2a</sub>in clinical practice: how to manage patients suffering from side effects
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosis
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Congenital adrenal hyperplasia
- Isoallopregnanolone reduces tic‐like behaviours in the D1 CT ‐7 mouse model of Tourette syndrome
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Indian Hedgehog Controls Proliferation and Differentiation in Skin Tumorigenesis and Protects against Malignant Progression
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Alopecia and Hirsuties
- Androgen Receptor Actions Modify Skin Structure and Chemical Carcinogen-induced Skin Cancer Susceptibility in Mice
- Genetic ablation of myelin protein zero-like 3 in mice increases energy expenditure, improves glycemic control, and reduces hepatic lipid synthesis
- 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
- Inhibition of 5α Reductase Impairs Cognitive Performance, Alters Dendritic Morphology and Increases Tau Phosphorylation in the Hippocampus of Male 3xTg-AD Mice
- Spontaneous cutaneous adverse drug reaction reports—An analysis of a 10‐year dataset in Singapore
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Protective cardiovascular and renal actions of vitamin D and estrogen
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Identifying molecular targets for reverse aging using integrated network analysis of transcriptomic and epigenomic changes during aging
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Isolation and Characterization of a Fetal-Maternal Microchimeric Stem Cell Population in Maternal Hair Follicles Long after Parturition
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatopathology and molecular genetics
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging