Search
for
Sort by
Research 241–270 of 1000+
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- Modulation of the differentiated phenotype of keratinocytes of the hair follicle and from epidermis
- ATP6AP1‐CDG: Follow‐up and female phenotype
- 0873 Modeling junctional epidermolysis bullosa using tissue-engineered skin substitutes
- 237 Unveiling Skin Cancers Pathophysiology via the Modeling of Xeroderma Pigmentosum Disease Modeling Using CRISPR-Cas9 Technology
- LB1059 Neuromediators associated with neurogenic skin inflammation promote M2 differentiation of macrophages in human skin ex vivo
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Store-operated calcium channels in skin
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- Natural killer cells in atopic and autoimmune diseases of the skin
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- TCDD-induced activation of aryl hydrocarbon receptor regulates the skin stem cell population
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- Transduction‐induced overexpression of Merkel cell T antigens in human hair follicles induces formation of pathological cell clusters with Merkel cell carcinoma‐like phenotype
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Through the lens of hair follicle neogenesis, a new focus on mechanisms of skin regeneration after wounding
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Characterization of the Role of Transferrin receptor 1 (Tfr1) in the Intestinal Epithelium, Pancreas, and Skin
- Impaired turnover of autophagolysosomes in cathepsin L deficiency
- Morpho-Regulation of Ectodermal Organs
- A missense mutation in Lama3 causes androgen alopecia
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis