Fol. Biol. 2017, 63, 165-173
Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease
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Novel Mutation (T273R) in Thyroid Hormone Receptor β Gene Provides Further Insight into Cryptic Negative Regulation by Thyroid Hormone
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Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients
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Prorenin Receptor Homologue VHA-20 is Critical for Intestinal pH Regulation, Ion and Water Management and Larval Development in
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Stress Perception and (GT)n Repeat Polymorphism in Haem Oxygenase 1 Promoter Are Both Risk Factors in Development of Eating Disorders
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Microsatellite Polymorphism in Haem Oxygenase 1 Gene Promoter in Multiple Sclerosis
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2012, Vol. 58, Issue 2, pp. 69-74 -
SMED-TLX-1 (NR2E1) Is Critical for Tissue and Body Plan Maintenance in Schmidtea mediterranea in Fasting/Feeding Cycles
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Genetic Variants in Haem Oxygenase-1 and Endothelial Nitric Oxide Synthase Influence the Extent and Evolution of Coronary Artery Atherosclerosis
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