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Research 121–150 of 1000+
- Graft versus host disease–like: A new paraneoplastic syndrome
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Identification of Potential Hub Genes in Alopecia Areata
- I‐Ascorbic acid 2‐phosphate represses the dihydrotestosterone‐induced dickkopf‐1 expression in human balding dermal papilla cells
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- INVESTIGATIONS INTO THE ROLE OF THE X-LINKED EPIGENETIC REGULATOR UTX (KDM6A) IN SELF-RENEWING STRATIFYING EPITHELIA
- Registrars’ Symposium: Summaries of Papers
- The TFIID subunit TAF4 regulates keratinocyte proliferation and has cell-autonomous and non-cell-autonomous tumour suppressor activity in mouse epidermis
- Assessment of Trial to Use Exosomes and Salmon DNA with Minoxidil as Multisource Mixture for Hair Follicle Activation an In Vivo Study
- Effects of oxytocin receptor agonists on hair growth promotion
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Research Snippets
- Genetic Differences between Male and Female Pattern Hair Loss in a Korean Population
- Hair Regenerative Mechanisms of Red Ginseng Oil and Its Major Components in the Testosterone-Induced Delay of Anagen Entry in C57BL/6 Mice
- Deletion of the <i>Sox21</i> gene drastically affects hair lipids
- Plain language summaries
- Hair Loss and Androgen’s Role in the Era of COVID-19
- 410 NON-INVASIVE DIAGNOSIS OF PROSTATE CANCER FROM BODY FLUIDS USING A PANEL OF TUMOR SUPPRESSOR GENES
- Polycomb repressive complex 2 in adult hair follicle stem cells is dispensable for hair regeneration
- EDA2R Is Associated with Androgenetic Alopecia
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- A missense mutation in Lama3 causes androgen alopecia
- Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Chapter-02 Androgenic Alopecia and Hirsutism
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2