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Research 601–630 of 1000+
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Differentiation capacity of stromal fibroblast-like cells from human bone marrow, adipose tissue, hair follicle dermal papilla and derma
- Halting the Progression of Cicatricial Alopecia with Injectable Platelet-Rich Fibrin
- Adipogenic Differentiation of Canine Hair Follicle Stem Cells (cHFSCs)
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Erosive Pustular Dermatosis: Delving into Etiopathogenesis and Management
- Uncommon Presentation of Pityriasis Rubra Pilaris of the Scalp: Clinical, Trichoscopic, and Histopathologic Features and Review of the Literature
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- JAK inhibition decreases the autoimmune burden in Down syndrome
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Recent advances in the genetics of alopecia areata
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Mesenchymal Stem Cell Secretome for Dermatology Application: A Review
- Genetic and molecular aspects of androgenetic alopecia
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Decision letter: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- scMC learns biological variation through the alignment of multiple single-cell genomics datasets
- Mesenchymal Stem Cell Secretome: Toward Cell-Free Therapeutic Strategies in Regenerative Medicine
- Challenges and Strategies for Improving the Regenerative Effects of Mesenchymal Stromal Cell-Based Therapies
- Conditioned Medium from Human Mesenchymal Stromal Cells: Towards the Clinical Translation
- Novel lysophosphoplipid receptors: their structure and function