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GATM (gene)
Functional Characterization of BC039389-GATM and KLK4
Laboratory Diagnosis of Creatine Deficiency Syndromes: a Technical Standard and Guideline of the American College of Medical Genetics and Genomics
Chuanxiong Rhizoma Compound on HIF-VEGF Pathway and Cerebral Ischemia-Reperfusion Injury’S Biological Network Based on Systematic Pharmacology
Inherited Renal Tubulopathies—Challenges and Controversies
Potential Role of Genomic Imprinted Genes and Brain Developmental
GATM Gene Glycine Amidinotransferase
Brain-Specific Functional Relationship Networks Inform Autism Spectrum
Regulation of Normal B-Cell Differentiation and Malignant B-Cell Survival by OCT2
GATM Mutations Cause a Dominant Fibrillar Conformational Disease In
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
GAMT, GATM Division of Human Genetics
Case Report of Cerebral Creatine Deficiency Syndrome with Novel Mutation of SLC6A8 Gene in a Male Child in Bangladesh
Polymorphism in the GATM Locus Associated with Dialysis-Independent Chronic Kidney Disease but Not Dialysis-Dependent Kidney Failure
Creatine Maintains Intestinal Homeostasis and Protects Against
(12) United States Patent (10) Patent No.: US 7.655,397 B2 Khan Et Al
Arginine:Glycine Amidinotransferase Deficiency
Anti-GATM Antibody (ARG58725)
Guide to Understanding CCDS Brochure
Top View
Characterization of Global Loss of Imprinting in Fetal Overgrowth Syndrome Induced by Assisted Reproduction
Investigating the Influence of Perinatal Nicotine and Alcohol Exposure On
Proteome Profile of Peripheral Myelin in Healthy Mice and in a Neuropathy
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure
Supp Tables 1-2.Pdf
GATM, the Human Ortholog of the Mouse Imprinted Gatm Gene, Escapes Genomic Imprinting in Placenta
Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder
For Peer Review 21 1 Medical Cell Biology, University Regensburg, Germany
Gatm, a Creatine Synthesis Enzyme, Is Imprinted in Mouse Placenta