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Research 151–180 of 161
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single‐cell RNA‐sequencing
- Heavy metals in biological samples of cancer patients: a systematic literature review
- Acrodermatitis Dysmetabolica with Concomitant Acquired Acrodermatitis Enteropathica in a Patient with Maple Syrup Urine Disease
- Bachmann–Bupp syndrome and treatment
- Schizochytrium sp. Extracted Lipids Prevent Alopecia by Enhancing Antioxidation and Inhibiting Ferroptosis of Dermal Papilla Cells
- 1447 Anti-senescence effect of extracellular vesicle from hyaluronic acid primed induced mesenchymal stem cells on aged human dermal fibroblast
- Examining the Effect of Notocactus ottonis Cold Vacuum Isolated Plant Cell Extract on Hair Growth in C57BL/6 Mice Using a Combination of Physiological and OMICS Analyses
- Curcumin-zinc framework encapsulated microneedle patch for promoting hair growth
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Acrodermatitis Enteropathica in an adult: a case report
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- 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
- Hair Follicle Stem Cell SLC3A2 Regulates Epithelial Regenerative Properties
- Identification of SLC40A1, LCN2, CREB5, and SLC7A11 as ferroptosis-related biomarkers in alopecia areata through machine learning
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- The ZIP7 Gene (Slc39a7) Encodes a Zinc Transporter Involved in Zinc Homeostasis of the Golgi Apparatus
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- The Biomedical Role of Zinc in the Functioning of the Human Organism
- An Infant with Worsening Rash
- CD98hc (<i>SLC3A2</i>) regulation of skin homeostasis wanes with age
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Iron Metabolism of the Skin: Recycling versus Release
- Fibronectin meshwork controls epithelial stem cell fate
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- 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