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Research 31–60 of 1000+
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Stem cell niches in mammals
- Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments
- Compartmentalized organization: a common and required feature of stem cell niches?
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Regulation of stem cell function by protein ubiquitylation
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- FGF5 is a crucial regulator of hair length in humans
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Frontiers in Topical Photoprotection
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Expression of Kruppel-Like Factor KLF4 in Mouse Hair Follicle Stem Cells Contributes to Cutaneous Wound Healing
- Hox genes in development and beyond
- Towards Defining the Pathogenesis of the Hairless Phenotype
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Morphogenetic Mechanisms in the Cyclic Regeneration of Hair Follicles and Deer Antlers from Stem Cells
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Research on the balance of thiol-disulfide in blood serum in women with telogen effluvium
- Endocrinology
- Apoptosis in Hair and Skin: A Review
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice