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RCAN1 gene
Known as:
Regulator of Calcineurin 1 Gene
, DOWN SYNDROME CRITICAL REGION GENE 1
, CALCIPRESSIN 1
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This gene is involved in modulation of protein phosphorylation.
National Institutes of Health
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Related topics
Related topics
7 relations
Calcipressin-1
DSCR10 gene
DSCR9 gene
Down Syndrome
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RCAN1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Chronic Expression of RCAN1-1L Protein Induces Mitochondrial Autophagy and Metabolic Shift from Oxidative Phosphorylation to Glycolysis in Neuronal Cells*
G. Ermak
,
S. Sojitra
,
F. Yin
,
E. Cadenas
,
A. Cuervo
,
K. Davies
Journal of Biological Chemistry
2012
Corpus ID: 5719861
Background: RCAN1s are stress-inducible proteins that have been shown to bind to the adenine nucleotide translocator (ANT…
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2012
2012
The phosphatase calcineurin PP2BAβ mediates part of mineralocorticoid receptor transcriptional activity
Anja Seiferth
,
S. Ruhs
,
S. Mildenberger
,
M. Gekle
,
C. Grossmann
The FASEB Journal
2012
Corpus ID: 19772102
Recently it was shown that the mineralocorticoid receptor (MR) may exert part of its transcriptional activity by mediation of…
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2012
2012
Lymphocytes from young healthy persons carrying the ApoE4 allele overexpress stress-related proteins involved in the pathophysiology of Alzheimer's disease.
M. Badia
,
A. Lloret
,
+4 authors
J. Viña
Journal of Alzheimer's Disease
2012
Corpus ID: 23784714
Apolipoprotein E4 (ApoE4) is a major genetic risk factor for the development of Alzheimer's disease (AD). The aim of this work…
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2009
2009
Regulator of Calcineurin (RCAN1-1L) Is Deficient in Huntington Disease and Protective against Mutant Huntingtin Toxicity in Vitro*
G. Ermak
,
Karl J. Hench
,
Kevin Chang
,
S. Sachdev
,
K. Davies
Journal of Biological Chemistry
2009
Corpus ID: 1380393
Our work suggests an important new link between the RCAN1 gene and Huntington disease. Huntington disease is caused by expansion…
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2008
2008
NF-κB-inducing Kinase Phosphorylates and Blocks the Degradation of Down Syndrome Candidate Region 1*
E. Lee
,
S. Seo
,
J. Um
,
Joongkyu Park
,
Yohan Oh
,
K. Chung
Journal of Biological Chemistry
2008
Corpus ID: 37094072
Down syndrome, the most frequent genetic disorder, is characterized by an extra copy of all or part of chromosome 21. Down…
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2008
2008
Regulation of vascular function by RCAN1 (ADAPT78).
D. V. Riper
,
L. Jayakumar
,
+4 authors
D. Crawford
Archives of Biochemistry and Biophysics
2008
Corpus ID: 205195383
2007
2007
Down Syndrome Critical Region-1 Is a Transcriptional Target of Nuclear Factor of Activated T Cells-c1 within the Endocardium during Heart Development*
Hai-liang Wu
,
S. Kao
,
+5 authors
C. Chang
Journal of Biological Chemistry
2007
Corpus ID: 19547565
Patients with Down syndrome have characteristic heart valve lesions resulting from endocardial cushion defects. The Down syndrome…
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Highly Cited
2004
Highly Cited
2004
DSCR1 gene expression is dependent on NFATc1 during cardiac valve formation and colocalizes with anomalous organ development in trisomy 16 mice.
Alexander W. Lange
,
J. Molkentin
,
K. Yutzey
Developmental Biology
2004
Corpus ID: 12210376
Highly Cited
2003
Highly Cited
2003
Oxidative and calcium stress regulate DSCR1 (Adapt78/MCIP1) protein.
Hung Yun Lin
,
H. Michtalik
,
+9 authors
D. Crawford
Free Radical Biology & Medicine
2003
Corpus ID: 26769281
2000
2000
Detection of two novel large deletions in SLC3A1 by semi‐quantitative fluorescent multiplex PCR
J. Purroy
,
L. Bisceglia
,
J. Jaeken
,
P. Gasparini
,
M. Palacín
,
V. Nunes
Human Mutation
2000
Corpus ID: 30821968
Cystinuria is an autosomal recessive aminoaciduria in which two clinical types have been described (type I and non‐type I…
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