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Research 181–210 of 1000+
- What causes hidradenitis suppurativa ?—15 years after
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Morphological Approach to Hair Disorders
- Alopecia Areata
- Dermal Papilla Cell-Derived Extracellular Vesicles Increase Hair Inductive Gene Expression in Adipose Stem Cells via β-Catenin Activation
- Dermatopathology and molecular genetics
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- The clock within
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- 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
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- <i>Hoxc13</i> mutant mice lack external hair
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Learning from nudity: lessons from the nude phenotype
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Concerted gene duplications in the two keratin gene families
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia