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Research 541–570 of 1000+
- Essential Role for Integrin-Linked Kinase in Melanoblast Colonization of the Skin
- μ-Crystallin in Mouse Skeletal Muscle Promotes a Shift from Glycolytic toward Oxidative Metabolism
- New Horizons in the Genetics of Polycystic Ovary Syndrome: From Predisposition to Precision Medicine.
- A Single-Arm, Open-Label, Phase Ib Clinical Study Evaluating the Efficacy and Safety of Durvalumab in Combination with Albumin-Bound Paclitaxel and Carboplatin as Neoadjuvant Therapy for Resectable Stage III Non-Small Cell Lung Cancer
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Androgen receptor activation integrates complex transcriptional effects in osteoblasts, involving the growth factors TGF-β and IGF-I, and transcription factor C/EBPδ
- Decision letter: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- O21 Single-cell RNA sequencing and proteomic analysis of dermal fibroblasts cultured from female scalp identifies significant alterations in cell populations with age
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- SFRP2/DPP4 and FMO1/LSP1 Define Major Fibroblast Populations in Human Skin
- GhDET2, a steroid 5α‐reductase, plays an important role in cotton fiber cell initiation and elongation
- The activin binding proteins follistatin and follistatin-related protein are differentially regulated in vitro and during cutaneous wound repair
- Epigen Transgenic Mice Develop Enlarged Sebaceous Glands
- Non-canonical dimerization of the androgen receptor and other nuclear receptors: implications for human disease
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- URB expression in human dermal papilla cells
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- Hair Follicle Stem Cell SLC3A2 Regulates Epithelial Regenerative Properties
- Mesenchymal Meis2 controls whisker development independently from trigeminal sensory innervation
- Faculty Opinions recommendation of The Venus flytrap trigger hair-specific potassium channel KDM1 can reestablish the K+ gradient required for hapto-electric signaling.
- Generating LacZ-reporter transgenic mice to identify α1 (XIX) Collagen (Col19a1) expression in Dermal Papilla Cells
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- The Membrane-Anchored <i>BOTRYTIS-INDUCED KINASE1</i> Plays Distinct Roles in <i>Arabidopsis</i> Resistance to Necrotrophic and Biotrophic Pathogens
- The role of AUTS2 in neurodevelopment and human evolution
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp