Search
for
Sort by
Research 241–270 of 1000+
- The roles of autophagy and apoptosis in burn wound progression in rats
- Unraveling the mechanism of action of cepharanthine for the treatment of novel coronavirus pneumonia (COVID-19) from the perspectives of systematic pharmacology
- Influence of Immune Cells and Circulating Inflammatory Cytokines on Pathological Scars: A Mendelian Randomization Study
- Hair Follicle Pigmentation
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Reprogramming adult dermis to a neonatal state through epidermal activation of β-catenin
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Bone morphogenetic protein signaling regulates the size of hair follicles and modulates the expression of cell cycle-associated genes
- Sex hormone binding globulin - an important biomarker for predicting PCOS risk: A systematic review and meta-analysis
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Neuroendocrine Perspectives in Alopecia Areata: Does Stress Play a Role?
- β-Catenin Signaling Increases in Proliferating NG2+ Progenitors and Astrocytes during Post-Traumatic Gliogenesis in the Adult Brain
- TRPV1 Function in Health and Disease
- Male pattern hair loss: current understanding
- Menopause and aging, quality of life and sexuality
- Cystoid macular oedema in uveitis: An unsolved problem
- An overview of JAK/STAT pathways and JAK inhibition in alopecia areata
- GABA<sub>A</sub>receptor modulation by neurosteroids in models of temporal lobe epilepsies
- The mineralocorticoid receptor as a novel player in skin biology: beyond the renal horizon?
- Ethanol intake patterns in female mice: Influence of allopregnanolone and the inhibition of its synthesis
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Comparative Transcriptome Analysis of the Regenerating Zebrafish Telencephalon Unravels a Resource With Key Pathways During Two Early Stages and Activation of Wnt/β-Catenin Signaling at the Early Wound Healing Stage
- Association analysis of oestrogen receptor beta gene ( <i>ESR2</i> ) polymorphisms with female pattern hair loss
- A mouse model of vitiligo based on endogenous auto-reactive CD8 + T cell targeting skin melanocyte
- Validation of the Alopecia Areata Patient Priority Outcomes (AAPPO) Questionnaire in Adults and Adolescents with Alopecia Areata
- lncRNA H19 acts as a ceRNA to regulate the expression of CTGF by targeting miR-19b in polycystic ovary syndrome
- Hair and scalp disorders in women of African descent: an overview
- Practical management of hair loss.
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss