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Research 721–750 of 1000+
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Mucosal TLR5 activation controls healthspan and longevity
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Dicer- and BSC-dependent miRNAs during murine anagen development
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- The amazing miniorgan: Hair follicle
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Systemic humoral activation facilitates tissue regeneration by D-chiral biomaterial scaffolds
- Skin manifestations of hyperandrogenism: an update
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- 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
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Exploring differential gene expression and biomarker potential in systemic lupus erythematosus: a retrospective study
- Recombinant Type XVII Collagen Promotes Hair Growth by Activating the Wnt/β-Catenin and SHH/GLI Signaling Pathways
- 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
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- Retinoic acid drives hair follicle stem cell activation via Wnt/β‐catenin signalling in androgenetic alopecia
- Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
- SP1 and KROX20 Regulate the Proliferation of Dermal Papilla Cells and Target the CUX1 Gene
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Repurposing DPP4-Inhibition to Improve Hair Follicle Activation and Regeneration
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation