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- 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
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Фрактальный обнаружитель эхo-сигнала
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Zinc and Zinc Transporters in Dermatology
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- The Biomedical Role of Zinc in the Functioning of the Human Organism
- Role of Zinc in Mucosal Health and Disease: A Review of Physiological, Biochemical, and Molecular Processes
- Generalized Dermatitis Caused by <i>Staphylococcus aureus</i> in the European Bison
- Alopecia induced in young mice by exposure to excess dietary zinc
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Inherited Acrodermatitis Enteropathica
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- An Infant with Worsening Rash
- Distinct transcriptomic landscapes of cutaneous basal cell carcinomas and squamous cell carcinomas
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Comparison of Mineral Levels in Blood and Hair Samples of Healthy Adults: Evaluating the Clinical Utility of Hair Mineral Analysis
- 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
- The Function of Zinc in Animal, Plant, and Human Nutrition