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TANGO2
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
22Q11 Deletion Syndrome: Current Perspective
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Abstract Book (PDF)
Platform Abstracts
Genetics MOLECULAR and HUMAN GENETICS 2021
SUPPLEMENTARY MATERIALS and METHODS PBMC Transcriptomics
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Us 2018 / 0305689 A1
TANGO2: Expanding the Clinical Phenotype and Spectrum of Pathogenic Variants
Biochemical Genetics
Cytogenomic SNP Microarray Abnormal * Patient: Patient
Tango2 Conference
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
By Submitted in Partial Satisfaction of the Requirements for Degree of in in the GRADUATE DIVISION of the UNIVERSITY of CALIFORN
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Differences Between Dorsal Root and Trigeminal Ganglion Nociceptors in Mice Revealed by Translational Profiling
Identification and Characterisation of the Underlying Defects in Patients with Inherited Platelet Bleeding Disorders
Top View
Inherited Metabolic Disorders Presenting with Ataxia
Copy Number Variation at 22Q11.2: from Rare Variants to Common Mechanisms of Developmental Neuropsychiatric Disorders
Blackwood, EA, Hofmann, C, Domingo, MS
Correlated Gene Modules Uncovered by Single-Cell Transcriptomics with High Detectability and Accuracy Authors: Alec R
The Phenotype Associated with Variants in TANGO2 May Be Explained by a Dual Role of the Protein in ER-To-Golgi Transport and at the Mitochondria
Comparative Mapping of the 22Q11. 2 Deletion Region and the Potential of Simple Model Organisms
Db171195supplementarydata2.Pdf
Mayer-Rokitansky-Küster-Hauser
Defining the Effect of the 16P11.2 Duplication on Cognition, Behavior, and Medical Comorbidities
Table of Contents List of Investigators
Identification of New Therapeutic Targets in CRLF2-Overexpressing B-ALL Through Discovery of 2 TF-Gene Regulatory Interactions
Exome Sequencing of Pakistani Consanguineous Families Identifies
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
(A) OX40 Expression on Intratumoral Pdc from HPV-Positive (N= 43) and HPV-Negative (N= 46) HNSCC Patients
Clinical Presentation and Proteomic Signature of Patients with TANGO2 Mutations
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle By
(2018) Investigating the Role of NF-Κb P50 Serine 80 Phosphorylation in the Regulation of Inflammation
JCI Suppli Fig1 Revised Ver1のコピー