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Research 631–660 of 1000+
- Androgen Receptor Actions Modify Skin Structure and Chemical Carcinogen-induced Skin Cancer Susceptibility in Mice
- Promoting axonal regeneration through exosomes: An update of recent findings on exosomal PTEN and mTOR modifiers
- 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
- 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
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Isolation and Characterization of a Fetal-Maternal Microchimeric Stem Cell Population in Maternal Hair Follicles Long after Parturition
- Dermatopathology and molecular genetics
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Metabolic dysfunction in female mice with disruption of 5α-reductase 1
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Different Requirements for GFRα2-Signaling in Three Populations of Cutaneous Sensory Neurons
- Lineage Tracing of Hair Follicle Stem Cells in Epidermal Whole Mounts
- Drug eruptions in dermatology
- The hair shaft: normality, abnormality, and genetics
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Epidermal growth factor, innovation and safety
- Association of vitamin D level with alopecia areata
- Hyperandrogenism in Adolescent Girls
- Decorin promotes proliferation and migration of ORS keratinocytes and maintains hair anagen in mice
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Dermoscopy: not just for dermatologists
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review