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TMEM1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
The Genetics of Bipolar Disorder
The Genetic Architecture of Down Syndrome Phenotypes Revealed by High-Resolution Analysis of Human Segmental Trisomies
WO 2012/174282 A2 20 December 2012 (20.12.2012) P O P C T
Chromosome 21 Leading Edge Gene Set
Orphanet Journal of Rare Diseases Biomed Central
Down Syndrome Congenital Heart Disease: a Narrowed Region and a Candidate Gene Gillian M
Supplementary Tables S1-S3
Low Replicative Stress Triggers Cell-Type Specific Inheritable
Analysis Identifies Signature Genes That Distinguish Microglia From
Chromosome 21: a Small Land of Fascinating Disorders with Unknown Pathophysiology
Kazuhiko Kawasaki
510(K) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY
Gene Expression Analysis of Cultured Amniotic Fluid Cell with Down Syndrome by DNA Microarray
Classification of Variations of HSA21 Gene Expression in Down Syndrome Lymphoblastoid Cell Lines : Impact on Disease Phenotype E
Downloaded from the Mouse Lysosome Gene Database, Mlgdb
Perfect Conserved Linkage Across the Entire Mouse Chromosome 10 Region Homologous to Human Chromosome 21
Differential Gene Expression and Specific Gene Duplications
Top View
CAETANO-DISSERTATION-2016.Pdf
Method for the Development of Gene Panels For
Supplementary Figure 1. Comparison Between the Amino Acid Composition Of
A Comprehensive Analysis of Allelic Methylation Status of Cpg Islands
Obesity and Obesogenic Growth Are Both Highly Heritable and Modified by Diet in a Nonhuman Primate Model, the African Green Monk
TMEM1 (TRAPPC10) (NM 003274) Human Recombinant Protein Product Data
Primepcr™Assay Validation Report
Genetic'dissection'of'growth'and' Meat'quality'traits'in'pigs''
An Integrated Analysis of Myeloid Cells Identifies Gaps in in Vitro Models of in Vivo Biology
Hamster PIWI Proteins Bind to Pirnas with Stage-Specific Size Variations During Oocyte Maturation
The Genetic Architecture of Down Syndrome Phenotypes Revealed by High-Resolution Analysis of Human Segmental Trisomies
Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
UC Irvine Electronic Theses and Dissertations
WO 2014/100434 Al 26 June 2014 (26.06.2014) W P O P C T
Long-Range Heterogeneity at the 3 Ends of Human Mrnas
Novel Bioinformatics Approaches for Microrna Detection and Target Prediction
I. Supplemental Methods A. Lipid Analysis B. Proteomics C. Gene Reporter (Luciferase) Assays D
Wo2018/191558
Genome-Wide Association Study on Detailed Profiles of Smoking
TRAPP Complexes in Secretion and Autophagy
Supplementary Table 1. a Full List of Cancer Genes
TMEM1 (S-19): Sc-79159
Gene Expression Profiling in the Adult Down Syndrome Brain ⁎ H.E