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Research 31–60 of 52
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Exploring the relationship between anastasis and mitochondrial ROS-mediated ferroptosis in metastatic chemoresistant cancers: a call for investigation
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Micronutrients in hair loss
- Biotin Is Required for the Zinc Homeostasis in the Skin
- Exploring extracellular vesicles as novel therapeutic agents for intervertebral disc degeneration: delivery, applications, and mechanisms
- Nutritional Dermatoses in the Hospitalized Patient
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- The ZIP7 Gene (Slc39a7) Encodes a Zinc Transporter Involved in Zinc Homeostasis of the Golgi Apparatus
- Table 1_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Table 2_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Inherited Acrodermatitis Enteropathica
- P78 Acrodermatitis enteropathica in children: clinical cases
- Zinc Spray for Treatment of Acrodermatitis Enteropathica: A Case Report
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Acquired Acrodermatitis Enteropathica in a 28-Year-Old Male with Type 1 Diabetes
- A Rare Case of Severe Acrodermatitis Enteropathica During Covid-19 Lockdown.
- Cyanidin 3-O-arabinoside suppresses DHT-induced dermal papilla cell senescence by modulating p38-dependent ER-mitochondria contacts
- Alopecia areata as a complication of hair restoration surgery
- Acrodermatitis Dysmetabolica with Concomitant Acquired Acrodermatitis Enteropathica in a Patient with Maple Syrup Urine Disease
- Curcumin-zinc framework encapsulated microneedle patch for promoting hair growth
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- The Biomedical Role of Zinc in the Functioning of the Human Organism
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica