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Research 30 of 161
- 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
- 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
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- Can hair be protected from oxidative damage during and after bleaching
- The Rotterdam Study: 2016 objectives and design update
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)