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Research 61–90 of 1000+
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- 757 Wound healing in aged skin exhibits systems-level alterations in cellular composition and cell-cell communication
- Skin deep: dermatologic challenges in PCOS through the female lifespan
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Laser therapy on darker ethnic skin
- Phenotypic variation in biotinidase deficiency
- Genomic and phenotypic characterization of Investigator Global Assessment (IGA) scale-based endotypes in atopic dermatitis
- Imbalanced redox dynamics induce fibroblast senescence leading to impaired stem cell pools and skin aging
- Pro‐Regenerative Hydrogel Restores Scarless Skin during Cutaneous Wound Healing
- Biomaterial-based mechanical regulation facilitates scarless wound healing with functional skin appendage regeneration
- Spectrum of Phenotypes Associated with Human MC1R Variations
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Prevalence of various phenotypes of polycystic ovarian syndrome among high school girls of Shiraz (2009)
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Persistently curly hair phenotype with the use of nivolumab for squamous cell lung cancer
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- Amelanocytic Anhidrotic Alopecia Areata-like Phenotype After Allogeneic Hematopoietic Cell Transplant
- Developing human fetal skin demonstrates a unique lymphocyte signature
- 1430 Modeling the onset of senescence associated secretory phenotype predicts therapeutic targets
- THE FREQUENCY OF VISCERAL AND PHENOTYPIC MARKERS IN PATIENTS WITH THE COMBINATION OF UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE AND GASTROESOPHAGEAL REFLUX DISEASE
- Phenotypic, transcriptomic, and genomic analyses reveal the spatiotemporal patterns and associated genes of coarse hair density in goats
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- 489 Seborrhea-like dermatitis phenotype in the Mpzl3 knockout mice
- Human Wharton’s Jelly Mesenchymal Stem Cells Plasticity Augments Scar-Free Skin Wound Healing with Hair Growth
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- 685 Modelling intrinsic and extrinsic cellular senescence in vitro with complex bioengineered human skin constructs
- LB1672 Senescent melanocytes in nevus skin stimulate hair growth