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Research 331–360 of 1000+
- Keratin disorders: from gene to therapy
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Physiologic functions of PP2A: Lessons from genetically modified mice
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Cell Types Promoting Goosebumps Form a Niche to Regulate Hair Follicle Stem Cells
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Localisation of members of the notch system and the differentiation of vibrissa hair follicles: Receptors, ligands, and fringe modulators
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The activin binding proteins follistatin and follistatin-related protein are differentially regulated in vitro and during cutaneous wound repair
- Regulation of masculinization: androgen signalling for external genitalia development
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Oxidative stress management in the hair follicle: Could targeting NRF2 counter age‐related hair disorders and beyond?
- Expression of<i>Sfrp2</i>Is Increased in Catagen of Hair Follicles and Inhibits Keratinocyte Proliferation
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Fibroblast heterogeneity and tertiary lymphoid tissues in the kidney
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Abstracts
- Depletion of S100A4+ stromal cells results in abnormal nipple development and nursing failure
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Prediction of male-pattern baldness from genotypes
- Surface modification and endothelialization of biomaterials as potential scaffolds for vascular tissue engineering applications
- Is dehydroepiandrosterone a hormone?
- The Rotterdam Study: 2016 objectives and design update