Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 222,815,796 papers from all fields of science
Search
Sign In
Create Free Account
GTF2I gene
Known as:
DIWS
, SPIN
, BAP135
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
GTF2I protein, human
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Role of Splice Variants of Gtf2i, a Transcription Factor Localizing at Postsynaptic Sites, and Its Relation to Neuropsychiatric Diseases
Yoshinori Shirai
,
Weidong Li
,
Tatsuo Suzuki
International Journal of Molecular Sciences
2017
Corpus ID: 16665266
We previously reported that various mRNAs were associated with postsynaptic density (PSD) purified from rat forebrain. Among the…
Expand
2016
2016
Proteomic analysis of SRF associated transcription complexes identified TFII-I as modulator of SRF function in neurons.
Christopher Meyer zu Reckendorf
,
S. Anastasiadou
,
F. Bachhuber
,
M. Franz‐Wachtel
,
B. Macek
,
B. Knöll
European Journal of Cell Biology
2016
Corpus ID: 207221278
2009
2009
New TFII-I family target genes involved in embryonic development.
A. Makeyev
,
D. Bayarsaihan
Biochemical and Biophysical Research…
2009
Corpus ID: 1488549
2005
2005
Multiple GTF2I-like Repeats of General Transcription Factor 3 Exhibit DNA Binding Properties
D. Vullhorst
,
A. Buonanno
Journal of Biological Chemistry
2005
Corpus ID: 10781878
A hallmark of general transcription factor 3 (GTF3) is the presence of multiple GTF2I-like repeats that were suggested to mediate…
Expand
2005
2005
Delivery management water requirement for irrigation ditches associated with large-sized paddy plots in Korea
Jin-soo Kim
,
S. Oh
,
K. Oh
,
Jaegab Cho
Paddy and Water Environment
2005
Corpus ID: 10766934
Delivery management water requirement (DMWR) is the use of bypass water in paddy field irrigation to help maintain desired water…
Expand
Highly Cited
2003
Highly Cited
2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype–phenotype analysis of five families with deletions in the Williams syndrome region
C. Morris
,
C. Mervis
,
+11 authors
A. Stock
American Journal of Medical Genetics. Part A
2003
Corpus ID: 8129522
Most individuals with Williams syndrome (WS) have a 1.6 Mb deletion in chromosome 7q11.23 that encompasses the elastin (ELN) gene…
Expand
1999
1999
A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome
M. Tassabehji
,
M. Carette
,
C. Wilmot
,
D. Donnai
,
A. Read
,
K. Metcalfe
European Journal of Human Genetics
1999
Corpus ID: 25764730
Williams-Beuren syndrome (WS) is a developmental disorder caused by a hemizygous microdeletion of approximately 1.4 MB at…
Expand
1998
1998
A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region.
Y. Wang
,
L. Pérez-Jurado
,
U. Francke
Genomics
1998
Corpus ID: 28468088
We have cloned and characterized Gtf2i, the mouse homolog of human GTF2I (general transcription factor II-I), which encodes BAP…
Expand
1995
1995
Modified Ligands to FA and FB in Photosystem I
Lian Yu
,
I. R. Vassiliev
,
Y. Jung
,
D. Bryant
,
J. Golbeck
Journal of Biological Chemistry
1995
Corpus ID: 27863466
A Photosystem I (PS I) complex reconstituted with PsaC-C51D (aspartate in lieu of cysteine in position 51) shows light-induced…
Expand
1983
1983
A Monte Carlo study of the three-states antiferromagnetic Potts model in two dimensions
F. Fucito
1983
Corpus ID: 28588729
Using Monte Carlo methods the author studies the two-dimensional three-stages Potts model with antiferromagnetic nearest…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE