|  Help  |  About  |  Contact Us

Search our database by keyword

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 2601 to 2700 out of 2899 for Fmr1

<< First    < Previous  |  Next >    Last >>
0.057s

Categories

Hits by Pathway

Hits by Strain

Hits by Category

Type Details Score
HT Experiment
GSE140565 | Ribosome profiling and RNA-seq of Fragile X mouse brain cortex
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
•
•
•
•
•
Publication
26240334 | J:332980
First Author: Del'Guidice T
Year: 2015
Journal: Proc Natl Acad Sci U S A
Title: FXR1P is a GSK3β substrate regulating mood and emotion processing.
Volume: 112
Issue: 33
Pages: E4610-9
•
•
•
•
•
Publication
29730159 | J:292659
First Author: Zhang M
Year: 2018
Journal: Dig Liver Dis
Title: FXR deletion in hepatocytes does not affect the severity of alcoholic liver disease in mice.
Volume: 50
Issue: 10
Pages: 1068-1075
•
•
•
•
•
Publication
30803859 | J:291563
First Author: Kong B
Year: 2019
Journal: Dig Liver Dis
Title: FXR deficiency alters bile acid pool composition and exacerbates chronic alcohol induced liver injury.
Volume: 51
Issue: 4
Pages: 570-576
•
•
•
•
•
Publication
25456134 | J:218753
First Author: Cook D
Year: 2014
Journal: Cell Rep
Title: FXR1P limits long-term memory, long-lasting synaptic potentiation, and de novo GluA2 translation.
Volume: 9
Issue: 4
Pages: 1402-1416
•
•
•
•
•
Strain
MGI:5003714 | STOCK Tg(Fmr1-EGFP)HP76Gsat/Mmucd
Attribute String: mutant stock, transgenic
•
•
•
•
•
Genotype
Genotype
Symbol: Rr305/Rr305
Background: Not Specified
Zygosity: hm
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Rr305/Rr305
Background: involves: C57BL/6
Zygosity: hm
Has Mutant Allele: true
•
•
•
•
•
Strain
MGI:5557018 | B6NTac;B6N-A<tm1Brd> Cyfip1<tm2a(EUCOMM)Wtsi>/2WtsiH
Attribute String: coisogenic, targeted mutation, mutant strain
•
•
•
•
•
Strain
MGI:5556956 | B6NTac;B6N-A<tm1Brd> Cyfip1<tm2a(EUCOMM)Wtsi>/WtsiH
Attribute String: mutant strain, targeted mutation, coisogenic
•
•
•
•
•
Strain
MGI:5557099 | B6NTac;B6N-A<tm1Brd> Cyfip2<tm1a(EUCOMM)Wtsi>/WtsiBiat
Attribute String: mutant strain, targeted mutation
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2<+>
Background: (C57BL/6N x C57BL/6J)F1
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip1/Cyfip1<+>
Background: B6J.129S7-Cyfip1
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Nufip1/Nufip1<+>
Background: C57BL/6NCrl-Nufip1/Mmucd
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Fmr1/Fmr1 Fxr2/Fxr2
Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd
Zygosity: cx
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Fxr2/Fxr2<+>
Background: C57BL/6N-Fxr2/Bay
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2<+>
Background: involves: C57BL/6
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2<+>
Background: C57BL/6N-Cyfip2/Wtsi
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2 Tg(Dkk3-cre)D9Tfur/?
Background: involves: C3H * C57BL/6 * C57BL/6N
Zygosity: cn
Has Mutant Allele: true
•
•
•
•
•
Publication
32493902 | J:292550
First Author: Morimoto K
Year: 2020
Journal: Sci Rep
Title: Reverse genetics reveals single gene of every candidate on Hybrid sterility, X Chromosome QTL 2 (Hstx2) are dispensable for spermatogenesis.
Volume: 10
Issue: 1
Pages: 9060
•
•
•
•
•
Publication
25486200 | J:229379
First Author: Hukema RK
Year: 2014
Journal: Cell Cycle
Title: Induced expression of expanded CGG RNA causes mitochondrial dysfunction in vivo.
Volume: 13
Issue: 16
Pages: 2600-8
•
•
•
•
•
Publication
10903848 | J:63605
First Author: Wu M
Year: 2000
Journal: Genomics
Title: An integrated deletion and physical map encompassing l71Rl, a chromosome 7 locus required for peri-implantation survival in the mouse.
Volume: 67
Issue: 2
Pages: 228-31
•
•
•
•
•
Publication
25588502 | J:221371
First Author: Beggs JE
Year: 2015
Journal: Biochem J
Title: The MAP kinase-interacting kinases regulate cell migration, vimentin expression and eIF4E/CYFIP1 binding.
Volume: 467
Issue: 1
Pages: 63-76
•
•
•
•
•
Publication
9712667 | J:49719
First Author: Qiao X
Year: 1998
Journal: J Neurosci
Title: Cerebellar brain-derived neurotrophic factor-TrkB defect associated with impairment of eyeblink conditioning in Stargazer mutant mice.
Volume: 18
Issue: 17
Pages: 6990-9
•
•
•
•
•
Strain
MGI:2159965 | C57BL/6N
Attribute String: inbred strain
•
•
•
•
•
Strain
MGI:2683688 | C57BL/6NCrl
Attribute String: inbred strain
•
•
•
•
•
Strain
MGI:5528299 | C57BL/6N-Cyfip2<M1N>/Cyfip2<tm1a(EUCOMM)Wtsi>
Attribute String: coisogenic, mutant strain, spontaneous mutation, targeted mutation
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2
Background: C57BL/6N-Cyfip2/Cyfip2
Zygosity: ht
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2<+> Fmr1/?
Background: involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NTac
Zygosity: cx
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Nufip1/Nufip1 S100a4/S100a4<+>
Background: involves: C57BL/6J
Zygosity: cn
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2 Shh/Shh<+>
Background: involves: C57BL/6
Zygosity: cn
Has Mutant Allele: true
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2<+> Eda/Eda
Background: involves: C57BL/6
Zygosity: cx
Has Mutant Allele: true
•
•
•
•
•
Publication
32212159 | J:296898
First Author: Tonelli Gombalová Z
Year: 2020
Journal: J Comp Neurol
Title: Majority of cerebrospinal fluid-contacting neurons in the spinal cord of C57Bl/6N mice is present in ectopic position unlike in other studied experimental mice strains and mammalian species.
Volume: 528
Issue: 15
Pages: 2523-2550
•
•
•
•
•
Publication
8895584 | -
First Author: Fridell RA
Year: 1996
Journal: EMBO J
Title: A nuclear role for the Fragile X mental retardation protein.
Volume: 15
Issue: 19
Pages: 5408-14
•
•
•
•
•
Publication
8842725 | -
First Author: Eberhart DE
Year: 1996
Journal: Hum Mol Genet
Title: The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals.
Volume: 5
Issue: 8
Pages: 1083-91
•
•
•
•
•
Publication
9285783 | -
First Author: Corbin F
Year: 1997
Journal: Hum Mol Genet
Title: The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes.
Volume: 6
Issue: 9
Pages: 1465-72
•
•
•
•
•
Publication
11719188 | -
First Author: Brown V
Year: 2001
Journal: Cell
Title: Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome.
Volume: 107
Issue: 4
Pages: 477-87
•
•
•
•
•
Publication
12147688 | -
First Author: Ohashi S
Year: 2002
Journal: J Biol Chem
Title: Identification of mRNA/protein (mRNP) complexes containing Puralpha, mStaufen, fragile X protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor.
Volume: 277
Issue: 40
Pages: 37804-10
•
•
•
•
•
Publication
14570712 | -
First Author: Ceman S
Year: 2003
Journal: Hum Mol Genet
Title: Phosphorylation influences the translation state of FMRP-associated polyribosomes.
Volume: 12
Issue: 24
Pages: 3295-305
•
•
•
•
•
Publication
12927206 | -
First Author: Chen L
Year: 2003
Journal: Neuroscience
Title: The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences.
Volume: 120
Issue: 4
Pages: 1005-17
•
•
•
•
•
Publication
14614133 | -
First Author: Todd PK
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95.
Volume: 100
Issue: 24
Pages: 14374-8
•
•
•
•
•
Publication
15317853 | -
First Author: Stefani G
Year: 2004
Journal: J Neurosci
Title: Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells.
Volume: 24
Issue: 33
Pages: 7272-6
•
•
•
•
•
Publication
15312650 | J:96571
First Author: Kanai Y
Year: 2004
Journal: Neuron
Title: Kinesin transports RNA: isolation and characterization of an RNA-transporting granule.
Volume: 43
Issue: 4
Pages: 513-25
•
•
•
•
•
Publication
16098134 | -
First Author: Antar LN
Year: 2005
Journal: Genes Brain Behav
Title: Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons.
Volume: 4
Issue: 6
Pages: 350-9
•
•
•
•
•
Publication
21490210 | -
First Author: Gross C
Year: 2011
Journal: J Neurosci
Title: Fragile X mental retardation protein regulates protein expression and mRNA translation of the potassium channel Kv4.2.
Volume: 31
Issue: 15
Pages: 5693-8
•
•
•
•
•
Publication
25692235 | -
First Author: Zhang Y
Year: 2014
Journal: RNA Biol
Title: FMRP interacts with G-quadruplex structures in the 3'-UTR of its dendritic target Shank1 mRNA.
Volume: 11
Issue: 11
Pages: 1364-74
•
•
•
•
•
Publication
10524236 | J:57450
First Author: Miyashita A
Year: 1999
Journal: Gene
Title: Five different genes, Eif4a1, Cd68, Supl15h, Sox15 and Fxr2h, are clustered in a 40 kb region of mouse chromosome 11.
Volume: 237
Issue: 1
Pages: 53-60
•
•
•
•
•
Publication
20530197 | J:162785
First Author: Naoe H
Year: 2010
Journal: Mol Cell Biol
Title: The anaphase-promoting complex/cyclosome activator Cdh1 modulates Rho GTPase by targeting p190 RhoGAP for degradation.
Volume: 30
Issue: 16
Pages: 3994-4005
•
•
•
•
•
Publication
28855249 | J:247276
First Author: Neppl RL
Year: 2017
Journal: J Cell Biol
Title: lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy.
Volume: 216
Issue: 11
Pages: 3497-3507
•
•
•
•
•
HT Experiment
GSE176449 | scRNAseq analysis of mouse WT and Fmr1KO dorsal root ganglions
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
•
•
•
•
•
Publication
11725301 | J:72894
First Author: McIntire JJ
Year: 2001
Journal: Nat Immunol
Title: Identification of Tapr (an airway hyperreactivity regulatory locus) and the linked Tim gene family.
Volume: 2
Issue: 12
Pages: 1109-16
•
•
•
•
•
Strain
MGI:3056279 | C57BL/6NJ
Attribute String: inbred strain
•
•
•
•
•
Strain
MGI:2164831 | C57BL/6NTac
Attribute String: inbred strain
•
•
•
•
•
Genotype
Genotype
Symbol: Cyfip2/Cyfip2<+> Shh/Shh<+>
Background: involves: C57BL/6
Zygosity: cn
Has Mutant Allele: true
•
•
•
•
•
Publication
- | J:100221
     
First Author: Oak Ridge National Laboratory
Year: 2005
Journal: Unpublished
Title: Information obtained from the Oak Ridge National Laboratory Mutant Mouse Database (ORNL), Oak Ridge, TN
•
•
•
•
•
Publication
34269176 | J:317350
   
First Author: O'Neil SD
Year: 2021
Journal: Elife
Title: Action potential-coupled Rho GTPase signaling drives presynaptic plasticity.
Volume: 10
•
•
•
•
•
Publication
8601493 | J:29903
First Author: Russell LB
Year: 1995
Journal: Genetics
Title: Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse.
Volume: 141
Issue: 4
Pages: 1547-62
•
•
•
•
•
Publication
23416452 | J:197462
First Author: Dillman AA
Year: 2013
Journal: Nat Neurosci
Title: mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortex.
Volume: 16
Issue: 4
Pages: 499-506
•
•
•
•
•
Publication
25313962 | J:259125
First Author: Yang J
Year: 2014
Journal: Dev Cell
Title: RBM24 is a major regulator of muscle-specific alternative splicing.
Volume: 31
Issue: 1
Pages: 87-99
•
•
•
•
•
HT Experiment
GSE147191 | Single Cell Transcriptomics Reveals Dysregulated Cellular and Molecular Networks in a Fragile X Syndrome Model
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
•
•
•
•
•
Publication
21946561 | J:180006
First Author: Yokoyama K
Year: 2011
Journal: EMBO J
Title: NYAP: a phosphoprotein family that links PI3K to WAVE1 signalling in neurons.
Volume: 30
Issue: 23
Pages: 4739-54
•
•
•
•
•
Publication
16930510 | J:113222
First Author: Li XY
Year: 2006
Journal: Reprod Fertil Dev
Title: Transcription profile during maternal to zygotic transition in the mouse embryo.
Volume: 18
Issue: 6
Pages: 635-45
•
•
•
•
•
Publication
15696166 | J:118818
First Author: Harikrishnan KN
Year: 2005
Journal: Nat Genet
Title: Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing.
Volume: 37
Issue: 3
Pages: 254-64
•
•
•
•
•
Publication
8307561 | J:16129
First Author: Arnaud D
Year: 1993
Journal: Genomics
Title: A panel of deleted mouse X chromosome somatic cell hybrids derived from the embryonic stem cell line HD3 shows preferential breakage in the Hprt-DXHX254E region.
Volume: 18
Issue: 3
Pages: 520-6
•
•
•
•
•
Protein
Q8BHG9
Organism: Mus musculus/domesticus
Length: 167  
Fragment?: false
•
•
•
•
•
Publication
25981527 | -
 
First Author: Agarwal P
Year: 2015
Journal: BMC Genomics
Title: CGGBP1 mitigates cytosine methylation at repetitive DNA sequences.
Volume: 16
Pages: 390
•
•
•
•
•
Publication
26482656 | -
First Author: Singh U
Year: 2015
Journal: Ups J Med Sci
Title: CGGBP1--an indispensable protein with ubiquitous cytoprotective functions.
Volume: 120
Issue: 4
Pages: 219-32
•
•
•
•
•
Publication
25483050 | -
First Author: Agarwal P
Year: 2016
Journal: Cell Cycle
Title: Growth signals employ CGGBP1 to suppress transcription of Alu-SINEs.
Volume: 15
Issue: 12
Pages: 1558-71
•
•
•
•
•
Publication
24196442 | -
First Author: Singh U
Year: 2014
Journal: Cell Cycle
Title: CGGBP1 phosphorylation constitutes a telomere-protection signal.
Volume: 13
Issue: 1
Pages: 96-105
•
•
•
•
•
Publication
31547883 | -
First Author: Patel D
Year: 2019
Journal: Epigenetics Chromatin
Title: CGGBP1 regulates CTCF occupancy at repeats.
Volume: 12
Issue: 1
Pages: 57
•
•
•
•
•
Protein Domain
IPR033375 | Cggbp1
Type: Family
Description: CGG triplet repeat-binding protein 1 (CGGBP1) is a repetitive DNA-binding transcription regulator with target sites at CpG-rich sequences such as CGG repeats and Alu-SINEs and L1-LINEs []. CGGBP1 mitigates cytosine methylation at repetitive DNA sequences []. It also functions in DNA damage/repair and telomere metabolism []. There are indications that it may be involved in mRNA metabolism []. CGGBP1 ensures CTCF occupancy preferentially on repeats over canonical CTCF motifs, being a regulator of CTCF and its binding sites in interspersed repeats [].CGGBP1/p20 is known to bind to nonmethylated 5'-d(CGG)(n)-3' trinucleotide repeats in the in the promoter of the fragile X messenger ribonucleoprotein 1 (FMR1/FMRP) gene [, ], although it seems not to have a direct effect on FMR1 transcription [].
•
•
•
•
•
Publication
28671696 | J:249721
First Author: Li J
Year: 2017
Journal: Nat Neurosci
Title: Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.
Volume: 20
Issue: 8
Pages: 1150-1161
•
•
•
•
•
Publication
27357688 | J:234235
First Author: Miyata H
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: Genome engineering uncovers 54 evolutionarily conserved and testis-enriched genes that are not required for male fertility in mice.
Volume: 113
Issue: 28
Pages: 7704-10
•
•
•
•
•
Publication
- | J:239583
     
First Author: Mouse Genome Informatics and the Consortium: Deciphering the Mechanisms of Developmental Disorders (DMDD)
Year: 2017
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from Deciphering the Mechanisms of Developmental Disorders (DMDD)
•
•
•
•
•
Publication
9562525 | J:47489
First Author: Oostra BA
Year: 1997
Journal: Ann Med
Title: Animal model for fragile X syndrome.
Volume: 29
Issue: 6
Pages: 563-7
•
•
•
•
•
Publication
15621528 | J:95806
First Author: Zarnescu DC
Year: 2005
Journal: Dev Cell
Title: Fragile X protein functions with lgl and the par complex in flies and mice.
Volume: 8
Issue: 1
Pages: 43-52
•
•
•
•
•
Publication
26319558 | J:318363
First Author: Jasińska M
Year: 2016
Journal: Mol Neurobiol
Title: miR-132 Regulates Dendritic Spine Structure by Direct Targeting of Matrix Metalloproteinase 9 mRNA.
Volume: 53
Issue: 7
Pages: 4701-12
•
•
•
•
•
Publication
10368286 | -
First Author: Lewis HA
Year: 1999
Journal: Structure
Title: Crystal structures of Nova-1 and Nova-2 K-homology RNA-binding domains.
Volume: 7
Issue: 2
Pages: 191-203
•
•
•
•
•
Publication
17437720 | -
First Author: García-Mayoral MF
Year: 2007
Journal: Structure
Title: The structure of the C-terminal KH domains of KSRP reveals a noncanonical motif important for mRNA degradation.
Volume: 15
Issue: 4
Pages: 485-98
•
•
•
•
•
Publication
17337072 | -
First Author: Matus-Ortega ME
Year: 2007
Journal: Biochim Biophys Acta
Title: The KH and S1 domains of Escherichia coli polynucleotide phosphorylase are necessary for autoregulation and growth at low temperature.
Volume: 1769
Issue: 3
Pages: 194-203
•
•
•
•
•
Publication
17159918 | -
First Author: Oddone A
Year: 2007
Journal: EMBO Rep
Title: Structural and biochemical characterization of the yeast exosome component Rrp40.
Volume: 8
Issue: 1
Pages: 63-9
•
•
•
•
•
Publication
1160884 | -
 
First Author: Gloor BP
Year: 1975
Journal: Mod Probl Ophthalmol
Title: [Transport of 131I-hippuric acid and 22Na from the space between retina and pigment epithelium after experimental amotio].
Volume: 15
Pages: 115-8
•
•
•
•
•
Publication
14618268 | -
First Author: Kruse C
Year: 2003
Journal: Cell Mol Life Sci
Title: The multi-KH protein vigilin associates with free and membrane-bound ribosomes.
Volume: 60
Issue: 10
Pages: 2219-27
•
•
•
•
•
Protein Domain
IPR004087 | KH_dom
Type: Domain
Description: The K homology (KH) domain was first identified in the human heterogeneous nuclear ribonucleoprotein (hnRNP) K. An evolutionarily conserved sequence of around 70 amino acids, the KH domain is present in a wide variety of nucleic acid-binding proteins. The KH domain binds RNA, and can function in RNA recognition []. It is found in multiple copies in several proteins, where they can function cooperatively or independently. For example, in the AU-rich element RNA-binding protein KSRP, which has 4 KH domains, KH domains 3 and 4 behave as independent binding modules to interact with different regions of the AU-rich RNA targets []. The solution structure of the first KH domain of FMR1 []and of the C-terminal KH domain of hnRNP K []determined by nuclear magnetic resonance(NMR) revealed a β-α-α-β-β-α structure. Proteins containing KH domains include:Bacterial and organelle PNPases [].Archaeal and eukaryotic exosome subunits [].Eukaryotic and prokaryotic RS3 ribosomal proteins [].Vertebrate Fragile X messenger ribonucleoprotein 1 (FMR1) [].Vigilin, which has 14 KH domains [].AU-rich element RNA-binding protein KSRP.hnRNP K, which contains 3 KH domains.Human onconeural ventral antigen-1 (NOVA-1) [].According to structural analyses [, , ], the KH domain can be separated in two groups - type 1 and type 2.
•
•
•
•
•
Publication
31330130 | J:282329
First Author: Hildebrandt MR
Year: 2019
Journal: Dev Biol
Title: Cytoplasmic aggregation of DDX1 in developing embryos: Early embryonic lethality associated with Ddx1 knockout.
Volume: 455
Issue: 2
Pages: 420-433
•
•
•
•
•
Publication
26586428 | J:228946
First Author: Wei N
Year: 2015
Journal: Cell Rep
Title: SRSF10 Plays a Role in Myoblast Differentiation and Glucose Production via Regulation of Alternative Splicing.
Volume: 13
Issue: 8
Pages: 1647-57
•
•
•
•
•
Publication
29539633 | J:261316
First Author: Perez-Garcia V
Year: 2018
Journal: Nature
Title: Placentation defects are highly prevalent in embryonic lethal mouse mutants.
Volume: 555
Issue: 7697
Pages: 463-468
•
•
•
•
•
Publication
19136466 | J:157426
First Author: Bensaid M
Year: 2009
Journal: Nucleic Acids Res
Title: FRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structure.
Volume: 37
Issue: 4
Pages: 1269-79
•
•
•
•
•
Publication
28499489 | J:323511
First Author: Michaelson JJ
Year: 2017
Journal: Biol Psychiatry
Title: Neuronal PAS Domain Proteins 1 and 3 Are Master Regulators of Neuropsychiatric Risk Genes.
Volume: 82
Issue: 3
Pages: 213-223
•
•
•
•
•
Publication
19377084 | J:149320
First Author: Hashem V
Year: 2009
Journal: Hum Mol Genet
Title: Ectopic expression of CGG containing mRNA is neurotoxic in mammals.
Volume: 18
Issue: 13
Pages: 2443-51
•
•
•
•
•
Publication
24108107 | J:205989
First Author: Yao B
Year: 2014
Journal: Hum Mol Genet
Title: Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome.
Volume: 23
Issue: 4
Pages: 1095-107
•
•
•
•
•
Publication
19436069 | J:151259
First Author: Wang H
Year: 2009
Journal: J Biol Chem
Title: Ca2+/calmodulin-dependent protein kinase IV links group I metabotropic glutamate receptors to fragile X mental retardation protein in cingulate cortex.
Volume: 284
Issue: 28
Pages: 18953-62
•
•
•
•
•
Publication
24336735 | J:205490
First Author: Padmashri R
Year: 2013
Journal: J Neurosci
Title: Altered structural and functional synaptic plasticity with motor skill learning in a mouse model of fragile X syndrome.
Volume: 33
Issue: 50
Pages: 19715-23
•
•
•
•
•
Publication
33276083 | J:302734
 
First Author: Torossian A
Year: 2021
Journal: Neurobiol Dis
Title: Increased rates of cerebral protein synthesis in Shank3 knockout mice: Implications for a link between synaptic protein deficit and dysregulated protein synthesis in autism spectrum disorder/intellectual disability.
Volume: 148
Pages: 105213
•
•
•
•
•
Publication
34349265 | J:326210
First Author: Ruth KS
Year: 2021
Journal: Nature
Title: Genetic insights into biological mechanisms governing human ovarian ageing.
Volume: 596
Issue: 7872
Pages: 393-397
•
•
•
•
•
Publication
14526173 | J:86289
First Author: Gu Y
Year: 2003
Journal: Cytogenet Genome Res
Title: FMR2 function: insight from a mouse knockout model.
Volume: 100
Issue: 1-4
Pages: 129-39
•
•
•
•
•
Publication
15564573 | J:96810
First Author: Gabel LA
Year: 2004
Journal: J Neurosci
Title: Visual experience regulates transient expression and dendritic localization of fragile X mental retardation protein.
Volume: 24
Issue: 47
Pages: 10579-83
•
•
•
•
•
Publication
22641815 | J:185984
First Author: Liu J
Year: 2012
Journal: Hum Mol Genet
Title: Signaling defects in iPSC-derived fragile X premutation neurons.
Volume: 21
Issue: 17
Pages: 3795-805
•
•
•
•
•
Publication
22914733 | J:188774
First Author: Lu C
Year: 2012
Journal: Hum Mol Genet
Title: Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice.
Volume: 21
Issue: 23
Pages: 5039-47
•
•
•
•
•
Publication
24763282 | J:226658
First Author: Metsu S
Year: 2014
Journal: PLoS Genet
Title: FRA2A is a CGG repeat expansion associated with silencing of AFF3.
Volume: 10
Issue: 4
Pages: e1004242
•
•
•
•
•




MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

Copyright © 2017 by The Jackson Laboratory. All Rights Reserved

© 2002 - 2017 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom