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GTF2IRD1
Program Nr: 1 from the 2004 ASHG Annual Meeting Mutations in A
Gene Expression Is Related to Parental Origin and Regional Coordinate Control
The Nuclear Localization Pattern and Interaction Partners of GTF2IRD1 Demonstrate a Role in Chromatin Regulation
GTF2IRD1 Rabbit Polyclonal Antibody – AP06760PU-N | Origene
Effects of Altered Gtf2i and Gtf2ird1 Expression on the Growth of Neural Progenitors and Organization of the Mouse Cortex
Integrative Prediction of Functionally Relevant Sumoylated Proteins
Determining the Genetic Contributions of the Williams Syndrome Critical Region to Behavior Using Mouse Models and Human Genetics
Williams Syndrome
RNA-Seq Analysis of Gtf2ird1 Knockout Epidermal Tissue Provides Potential Insights Into Molecular Mechanisms Underpinning Williams-Beuren Syndrome Susan M
GTF2IRD2 Is Located in the Williams–Beuren Syndrome Critical Region 7Q11.23 and Encodes a Protein with Two TFII-I-Like Helix–Loop–Helix Repeats
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
An Atypical 7Q11.23 Deletion in a Normal IQ Williams&Ndash
Essential Functions of the Williams-Beuren Syndrome-Associated TFII-I Genes in Embryonic Development
Genes Contained Within the Interval Between Rhbdd2 and D12rat8 (1.7Mb)§
An in Vivo Study of GTF2IRD1 Function and Its Contribution to the Physical Features of Williams Beuren Syndrome
The Molecular Role of GTF2IRD1: a Protein Involved in The
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
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AK005040 Ncf1 Gtf2i Gtf2ird1 Cyln2 Rfc2 Limk1 Eln Cldn4 AK017044
Neuroscore: a Genome-Wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System
Beuren Syndrome Associated Genes in Mouse Embryonic Stem Cells
Investigating the Influence of Perinatal Nicotine and Alcohol Exposure On
Copy Number Variants at Williams–Beuren Syndrome 7Q11.23 Region
Molecular Analysis of GTF2IRD1: a Protein Implicated in the Neurobehavioural Features of Williams-Beuren Syndrome
UCLA Previously Published Works
Maternal and Indirect Genetic Effects on Behavioural And
Poster Session I 2
Isolation and Characterisation of GTF2IRD2, a Novel Fusion Gene and Member of the TFII-I Family of Transcription Factors, Deleted in Williams–Beuren Syndrome
Transcriptomic Changes in the Pre-Implantation Uterus Highlight
GTF2IRD1 Gene GTF2I Repeat Domain Containing 1
New TFII-I Family Target Genes Involved in Embryonic Development Aleksandr V
1 1 Functions of Gtf2i and Gtf2ird1 in the Developing Brain
Spatiotemporal 7Q11.23 Protein Network Analysis Implicates the Role of DNA Repair Pathway During Human Brain Development
JCI Suppli Fig1 Revised Ver1のコピー
Atypical Deletion of Williams-Beuren Syndrome Reveals the Mechanism of Neurodevelopmental Disorders
Global Analysis of Gene Expression in the Developing Brain of Gtf2ird1