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Research 901–930 of 1000+
- Hair follicle regeneration suppresses Ras-driven oncogenic growth
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- Melatonin’s effect on hair follicles in a goat (Capra hircus) animal model
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Spatial transcriptomics of a giant pilomatricoma
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- Does Androgenic Alopecia Aggravate the Risk of Prostate Cancer? Evidence from Mendelian Randomization
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Structural insights into SARS-CoV-2 spike protein and its natural mutants found in Mexican population
- Alopecia in patients treated with molecularly targeted anticancer therapies
- Outcomes in Clinically Relevant Patient Subgroups From the EMBRACA Study: Talazoparib vs Physician’s Choice Standard-of-Care Chemotherapy
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Effective holistic characterization of small molecule effects using heterogeneous biological networks
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Wound Healing: A Cellular Perspective
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes