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Research 601–630 of 1000+
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- All‐Natural Immunomodulatory Bioadhesive Hydrogel Promotes Angiogenesis and Diabetic Wound Healing by Regulating Macrophage Heterogeneity
- Cultured dermal papilla cells from androgen-dependent human hair follicles (e.g. beard) contain more androgen receptors than those from non-balding areas of scalp
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Inflammatory priming enhances mesenchymal stromal cell secretome potential as a clinical product for regenerative medicine approaches through secreted factors and EV-miRNAs: the example of joint disease
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Multiple skin tumours in a Doberman Pinscher with colour dilution alopecia
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Skin as a Window to Endocrine Dysfunction: Dermatological and Metabolic Interactions in Polycystic Ovary Syndrome
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- Decision letter: Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- 1433 Epithelially derived, mitochondrial MPZL3 negatively regulates murine and human hair follicle cycling
- Criteria for Defining Polycystic Ovary Syndrome as a Predominantly Hyperandrogenic Syndrome: An Androgen Excess Society Guideline
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis
- ATP-competitive mTOR kinase inhibitors delay plant growth by triggering early differentiation of meristematic cells but no developmental patterning change
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Aromatase deficiency in a male patient - Case report and review of the literature.
- <i>WNT10A</i> , dermatology and dentistry
- Wnt Signaling Influences the Development of Murine Epidermal Langerhans Cells
- Making the head: Caspases in life and death
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review