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TMEM98
Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Product Datasheet Qprest
Supplemental Figure 1
Autosomal Dominant Nanophthalmos and High Hyperopia Associated with a C-Terminal Frameshift Variant in MYRF
UNIVERSITY of CALIFORNIA RIVERSIDE Impact of Alcohol on Intestinal Homeostasis a Dissertation Submitted in Partial Satisfaction
Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse
Identification of Expression Qtls Targeting Candidate Genes For
TMEM98 (C-18): Sc-241083
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Computational Proteogenomic Identification and Functional
Mutation in TMEM98 in a Large White Kindred with Autosomal Dominant Nanophthalmos Linked to 17P12-Q12
Agricultural University of Athens
TMEM98 (NM 015544) Human Recombinant Protein – TP301829
Missense Mutations in the Human Nanophthalmos Gene TMEM98
Distinct Transcriptomes Define Rostral and Caudal 5Ht Neurons
Molecular Signatures of the Pathogenesis ISBN-10: 90-9021312-0 ISBN-13: 978-90-9021312-5
Molecular and Systemic Functions of the Vertebrate-Specific
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Flipping the Hemoglobin Switch and Discovering Regulators Involved in Fetal Hemoglobin Reactivation
A Case Study Involving Hexagenia Spp
Identification of Expression Qtls Targeting Candidate Genes for Residual Feed Intake in Dairy Cattle Using Systems Genomics
Expression Profiling of Macrophages Reveals Multiple Populations With
Novel TMEM98, MFRP, PRSS56 Variants in a Large United States High Hyperopia and Nanophthalmos Cohort Lev Prasov1,2*, Bin Guan3, Ehsan Ullah3, Steven M
The Nanophthalmos Protein TMEM98 Inhibits MYRF Self-Cleavage and Is
Modeling Gene Regulation from Paired Expression and Chromatin Accessibility Data
Downloaded from the TCGA Database
Edematous Severe Acute Malnutrition Is Characterized by Hypomethylation of DNA
Novel TMEM98 Mutations in Pedigrees with Autosomal Dominant Nanophthalmos
Table S1 the Statistical Metrics for Key Differentially Expressed Genes (Degs)
An Epigenetic Mechanism for Cavefish Eye Degeneration
The Nanophthalmos Protein TMEM98 Inhibits MYRF Self-Cleavage and Is
Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
Characterization of Cellular and Molecular Heterogeneity of Bone Marrow Stromal Cells
Genomic Architecture of Schizophrenia Across Diverse
Wo2018/191558