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Research 931–960 of 1000+
- Kelulut Honey Regulates Sex Steroid Receptors in a Polycystic Ovary Syndrome Rat Model
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Dicer- and BSC-dependent miRNAs during murine anagen development
- Woolly Antics between the Sheaths
- Insights into the context-dependent immunological roles of the CXCL12–CXCR4 axis in alopecia
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Exploring differential gene expression and biomarker potential in systemic lupus erythematosus: a retrospective study
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Melatonin-Mediated Circadian Rhythm Signaling Exhibits Bidirectional Regulatory Effects on the State of Hair Follicle Stem Cells
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Autoimmunity and clinical pathology amelioration in SLE by Dexamethasone primed Mesenchymal Stem Cell derived conditioned media
- Topical sodium valproate-loaded nanospanlastics versus conventional topical steroid therapy in alopecia areata: a randomized controlled study
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Two females with hair loss
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Regenerative Medicine of Epidermal Structures
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Congenital hair loss disorders: Rare, but not too rare
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene