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Research 601–630 of 1000+
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Store-operated calcium channels in skin
- Runx Family Genes in Tissue Stem Cell Dynamics
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- [Proteomics-based screening of differentially expressed proteins in skin of Chinese merino fine sheep (JunKen type) of different gender].
- Specific In Vivo Ablation of Lrig1-Positive Follicular Progenitor Cells Results in Sebaceous Gland Loss in Mice
- Molecular Predictors of Ritlecitinib Efficacy in Alopecia Areata: Role of JAK3-Dependent Inflammation and Follicular Integrity
- The IVIG treatment response in autoimmune polyendocrine syndromes type 2 with anti-GAD65 antibody-associated stiff person syndrome: a case report and literature review
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- 361 p120-catenin regulates epidermal inflammation in a cadherin-dependent manner
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Innate lymphoid cells type 1 may be new, non-antigen-specific player in the pathogenesis of alopecia areata
- 1336 The de novo DNA methyltransferase DNMT3A is required for epidermal homeostasis
- 308 Epidermal keratinocytes regulate bacterial immune responses and host defense through EGFR
- Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ
- Wirkung von Testosteron auf Haut und Haare
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII
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- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
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- Research Snippets
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Loss of PIKFyve Kinase Function Driven by Platelet Factor 4 Promoter Results in Platelet Lysosomal Storage Defects and Infiltration of Multiple Organs with Vacuolated Macrophages
- Knowledge about androgenetic alopecia among women and men – a survey research
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- The transcriptional landscape of seasonal coat colour moult in the snowshoe hare
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Evaluation and Treatment of Gender Dysphoria to Prepare for Gender Confirmation Surgery