Related references
Note: Only part of the references are listed.Cohesins functionally associate with CTCF on mammalian chromosome arms
Vania Parelho et al.
CELL (2008)
A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10
Lionel A. Sanz et al.
EMBO JOURNAL (2008)
Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators
William Stedman et al.
EMBO JOURNAL (2008)
Type 2 diabetes mellitus in a non-obese mouse model induced by Meg 1/Grb10 overexpression
Yoshie Yamamoto et al.
EXPERIMENTAL ANIMALS (2008)
Mitogenic Roles of Gab 1 and Grb 10 as Direct Cellular Partners in the Regulation of MAP Kinase Signaling
Youping Deng et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2008)
Grb10/Nedd4-mediated multiubiquitination of the insulin-like growth factor receptor regulates receptor internalization
Giada Monami et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2008)
The endocrine phenotype in Silver-Russell syndrome is defined by the underlying epigenetic alteration
Gerhard Binder et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome:: paternal deletion of the epsilon-sarcoglycan (SGCE) gene
C. Bonnet et al.
JOURNAL OF HUMAN GENETICS (2008)
Molecular and clinical findings and their correlations in Silver-Russell syndrome:: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas
Kazuki Yamazawa et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2008)
Cohesin mediates transcriptional insulation by CCCTC-binding factor
Kerstin S. Wendt et al.
NATURE (2008)
QUMA: quantification tool for methylation analysis
Yuichi Kumaki et al.
NUCLEIC ACIDS RESEARCH (2008)
CTCF physically links cohesin to chromatin
Eric D. Rubio et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
The genetic aetiology of Silver-Russell syndrome
S. Abu-Amero et al.
JOURNAL OF MEDICAL GENETICS (2008)
Genomic imprinting of Dopa decarboxylase in heart and reciprocal allelic expression with neighboring Grb10
Trevelyan R. Menheniott et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: Clinical scoring system and epigenetic-phenotypic correlations
Irene Netchine et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)
Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome
Natalia T. Leach et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
High-resolution profiling of histone methylations in the human genome
Artern Barski et al.
CELL (2007)
Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10
Yoko Yamasaki-Ishizaki et al.
MOLECULAR AND CELLULAR BIOLOGY (2007)
Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain
T Eggermann et al.
JOURNAL OF MEDICAL GENETICS (2006)
Grb10 mediates insulin-stimulated degradation of the insulin receptor: a mechanism of negative regulation
Fresnida J. Ramos et al.
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM (2006)
Hypomethylation of the h19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype
J Bliek et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality
R Ono et al.
NATURE GENETICS (2006)
Bisulfite sequencing and dinucleotide content analysis of 15 imprinted mouse differentially methylated regions (DMRs): paternally methylated DMRs contain less CpGs than maternally methylated DMRs
H. Kobayashi et al.
CYTOGENETIC AND GENOME RESEARCH (2006)
The adapter protein GRB10 is an endogenous negative regulator of insulin-like growth factor signaling
AM Dufresne et al.
ENDOCRINOLOGY (2005)
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome
C Gicquel et al.
NATURE GENETICS (2005)
Meg1/Grb10 overexpression causes postnatal growth retardation and insulin resistance via negative modulation of the IGF1R and IR cascades
H Shiura et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
Distinct Grb10 domain requirements for effects on glucose uptake and insulin signaling
K Mori et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2005)
Negative regulation of insulin-stimulated mitogen-activated protein kinase signaling by Grb10
P Langlais et al.
MOLECULAR ENDOCRINOLOGY (2004)
Growth factor receptor-binding protein 10 (Grb10) as a partner of phosphatidylinositol 3-kinase in metabolic insulin action
YP Deng et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism
M Charalambous et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
The Grb10/Nedd4 complex regulates ligand-induced ubiquitination and stability of the insulin-like growth factor I receptor
A Vecchione et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
P Arnaud et al.
HUMAN MOLECULAR GENETICS (2003)
Grb10 inhibits insulin-stimulated insulin receptor substrate (IRS)-phosphatidylinositol 3-kinase/Akt signaling pathway by disrupting the association of IRS-1/IRS-2 with the insulin receptor
KR Wick et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes;: roles of brain-specific promoters and mouse-specific CTCF-binding sites
T Hikichi et al.
NUCLEIC ACIDS RESEARCH (2003)
DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed
MP Hitchins et al.
MAMMALIAN GENOME (2002)
Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region
D Monk et al.
HUMAN GENETICS (2002)
An evolutionarily conserved putative insulator element near the 3′ boundary of the imprinted Igf2/H19 domain
K Ishihara et al.
HUMAN MOLECULAR GENETICS (2002)
No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients
S Kobayashi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2001)
Evidence against GRB10 as the gene responsible for Silver-Russell syndrome
JA McCann et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21
R Ono et al.
GENOMICS (2001)
The BPS domain of Grb10 inhibits the catalytic activity of the insulin and IGF1 receptors
EG Stein et al.
FEBS LETTERS (2001)
Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB70 in Silver-Russell syndrome
MP Hitchins et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2001)
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion
N Blagitko et al.
HUMAN MOLECULAR GENETICS (2000)
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
AC Bell et al.
NATURE (2000)
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
AT Hark et al.
NATURE (2000)
Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome
D Monk et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Share Paper
