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Fig4
Mouse Germ Line Mutations Due to Retrotransposon Insertions Liane Gagnier1, Victoria P
Molecular Mechanisms Involved Involved in the Interaction Effects of HCV and Ethanol on Liver Cirrhosis
Protein Identities in Evs Isolated from U87-MG GBM Cells As Determined by NG LC-MS/MS
Mutations in Pi(3,5)P2 Signaling and Neurodegeneration in Mouse and Human
Identification of Transcriptional Mechanisms Downstream of Nf1 Gene Defeciency in Malignant Peripheral Nerve Sheath Tumors Daochun Sun Wayne State University
Loss of Pikfyve in Platelets Causes a Lysosomal Disease Leading to Inflammation and Thrombosis in Mice
Genetic Differences Between Extreme and Composite Constitution Types from Whole Exome Sequences Reveal Actionable Variations
Genetic and Functional Investigation of Inherited Neuropathies
FIG4 Variants in Central European Patients with Amyotrophic Lateral Sclerosis: a Whole-Exome and Targeted Sequencing Study
Tepzz 8Z6z54a T
Diagnostics of Halitosis Complaints by a Multidisciplinary Team
WO 2014/089124 Al 12 June 20 14 ( 12.06.20 14) W P O P C T
Supplemental Solier
Macaque Gene Symbols Were Mapped to Human Gene Symbols on June 2011
Mrna Expression in Human Leiomyoma and Eker Rats As Measured by Microarray Analysis
Supplementary Figure 1. Epigenomic Maps of Endocrine Therapy Sensitive and Resistant Cell Lines
WO 2016/004387 Al 7 January 2016 (07.01.2016) P O P C T
AAV9-Mediated FIG4 Delivery Prolongs Life Span in Charcot-Marie-Tooth Disease Type 4J Mouse Model
Top View
Supplementary File S4. Genes Within Each Module Mackay Et Al
Alteration of Gene Expression in Mammary Gland Tissue of 31 Dairy Cows in Response to Dietary Unsaturated Fatty Acids
Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Human
Protein List (6009)
Phosphatidylinositol 3,5Bisphosphate
Rab35-Regulated Lipid Turnover by Myotubularins Represses Mtorc1 Activity and Controls Myelin Growth
(Human and Monkey) and Mouse Pscs Mouse Primed
Comparison of Genes Expressed in Primed States of Human And
Doctoral Dissertation by Yongsheng Huang
1 Reference Sequence Number Gene Symbol Alleles Chromosomal
ABSTRACT Gene Expression Profiling to Understand the Alterations In
Role of the Phosphoinositide Phosphatase FIG4 Gene in Familial Epilepsy with Polymicrogyria
Screening for Mutations in the Genes VCP and KIAA0196 in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Supplementary Table 1. Table of 16 Gene Classes Based on Age-Specific Expression
Comprehensive Genetic Test Menu
Supplementary File 2B Revised
Yunis-Varon Syndrome Is Caused by Mutations in FIG4
Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Human