Search
for
Sort by
Research 811–840 of 1000+
- Industry updates in advanced therapy medicinal products and regenerative medicine – March 2026
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- Fibroblast Growth Factor-7 and Hair Biology: Bridging Basic Science and Therapeutic Applications
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Who Tells the Story of the Treatment of Androgenetic Alopecia?—A Bibliometric Analysis From 2003 to 2023
- The GPR30 agonist G-1 promotes hair growth via Wnt/Hedgehog signaling in mice
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Disturbance of Immune Microenvironment in Androgenetic Alopecia through Spatial Transcriptomics
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- Effects of Natural Herbal Marker Compounds on Human Dermal Papilla Cell Growth Regulation
- A missense mutation in Lama3 causes androgen alopecia
- Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders
- Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein
- Bachmann–Bupp syndrome and treatment
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Pathogenesis of androgenetic alopecia
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Divergent genetic mechanism leads to spiny hair in rodents
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Generalized atrophic benign epidermolysis bullosa.
- Control by a hair’s breadth: the role of microRNAs in the skin
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Optimal processing for proteomic genotyping of single human hairs
- Evolution of Trichocyte Keratins