11733-1-AP
antibody from Proteintech Group
Targeting: CUX1
CASP, CDP, CDP/Cut, CDP/Cux, CDP1, Clox, CUT, CUTL1, CUX, Cux/CDP, GOLIM6
Antibody data
- Antibody Data
- Antigen structure
- References [58]
- Comments [0]
- Validations
- Western blot [1]
- Immunocytochemistry [1]
Submit
Validation data
Reference
Comment
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- Product number
- 11733-1-AP - Provider product page
- Provider
- Proteintech Group
- Proper citation
- Proteintech Cat#11733-1-AP, RRID:AB_2086995
- Product name
- CUX1 antibody
- Antibody type
- Polyclonal
- Description
- KD/KO validated CUX1 antibody (Cat. #11733-1-AP) is a rabbit polyclonal antibody that shows reactivity with human, mouse, rat and has been validated for the following applications: IF, IHC, IP, WB,ELISA.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references Cortico-thalamic communication for action coordination in a skilled motor sequence.
BRN1/2 Function in Neocortical Size Determination and Microcephaly.
Cell type specific roles of FOXP1 during early neocortical murine development.
iPSC-derived models of PACS1 syndrome reveal transcriptional and functional deficits in neuron activity.
A C-terminal motif containing a PKC phosphorylation site regulates γ-Protocadherin-mediated dendrite arborization in the cerebral cortex in vivo.
Disruption of lysosomal nutrient sensing scaffold contributes to pathogenesis of a fatal neurodegenerative lysosomal storage disease.
Neonatal brain injury unravels transcriptional and signaling changes underlying the reactivation of cortical progenitors.
The GDNF-gel/HA-Mg conduit promotes the repair of peripheral nerve defects by regulating PPAR-γ/RhoA/ROCK signaling pathway.
Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model.
P53 independent pathogenic mechanisms contribute to BubR1 microcephaly.
Taok1 haploinsufficiency leads to autistic-like behaviors in mice via the dorsal raphe nucleus.
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.
Pituitary adenylate cyclase-activating polypeptide deficient mice show length abnormalities of the axon initial segment.
Stem cell competition driven by the Axin2-p53 axis controls brain size during murine development.
Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder.
Notch directs telencephalic development and controls neocortical neuron fate determination by regulating microRNA levels.
A Robust Pipeline for the Multi-Stage Accelerated Differentiation of Functional 3D Cortical Organoids from Human Pluripotent Stem Cells.
An entosis-like process induces mitotic disruption in Pals1 microcephaly pathogenesis.
Effect of CUX1 on the Proliferation of Hu Sheep Dermal Papilla Cells and on the Wnt/β-Catenin Signaling Pathway.
RNA methylation-related genes of m6A, m5C, and m1A predict prognosis and immunotherapy response in cervical cancer.
An adhesion signaling axis involving Dystroglycan, β1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold.
Npas3 regulates stemness maintenance of radial glial cells and neuronal migration in the developing mouse cerebral cortex.
Astrocytic Piezo1-mediated mechanotransduction determines adult neurogenesis and cognitive functions.
Increased glycine contributes to synaptic dysfunction and early mortality in Nprl2 seizure model.
TMEM106B deficiency impairs cerebellar myelination and synaptic integrity with Purkinje cell loss.
Divergent transcriptional regulation of astrocyte reactivity across disorders.
CUX1 promotes epithelial-mesenchymal transition (EMT) in renal fibrosis of UUO model by targeting MMP7.
Post-GWAS functional analysis identifies CUX1 as a regulator of p16(INK4a) and cellular senescence.
Length impairments of the axon initial segment in rodent models of attention-deficit hyperactivity disorder and autism spectrum disorder.
Merkel cell polyomavirus small T antigen is a viral transcription activator that is essential for viral genome maintenance.
GRN-/- iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis.
Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.
Restoration of Visual Function and Cortical Connectivity After Ischemic Injury Through NeuroD1-Mediated Gene Therapy.
CUX1 Facilitates the Development of Oncogenic Properties Via Activating Wnt/β-Catenin Signaling Pathway in Glioma.
Neuroserpin Is Strongly Expressed in the Developing and Adult Mouse Neocortex but Its Absence Does Not Perturb Cortical Lamination and Synaptic Proteome.
RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity.
IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype.
Cellular and Behavioral Characterization of Pcdh19 Mutant Mice: subtle Molecular Changes, Increased Exploratory Behavior and an Impact of Social Environment.
Centrosome defects cause microcephaly by activating the 53BP1-USP28-TP53 mitotic surveillance pathway.
Overexpressed P75CUX1 promotes EMT in glioma infiltration by activating β-catenin.
Astragalus polysaccharide regulates brown adipogenic differentiation through miR-1258-5p-modulated cut-like homeobox 1 expression.
miR-143 Targeting CUX1 to Regulate Proliferation of Dermal Papilla Cells in Hu Sheep.
Differential Expression Levels of Sox9 in Early Neocortical Radial Glial Cells Regulate the Decision between Stem Cell Maintenance and Differentiation.
ZBTB20 is crucial for the specification of a subset of callosal projection neurons and astrocytes in the mammalian neocortex.
Cut-like homeobox 1 (CUX1) tumor suppressor gene haploinsufficiency induces apoptosis evasion to sustain myeloid leukemia.
AIF3 splicing switch triggers neurodegeneration.
Liquid Biopsy of Extracellular Vesicle-Derived miR-193a-5p in Colorectal Cancer and Discovery of Its Tumor-Suppressor Functions.
hGFAP-Positive Stem Cells Depend on Brg1 for Proper Formation of Cerebral and Cerebellar Structures.
Reversing a model of Parkinson's disease with in situ converted nigral neurons.
The basic helix-loop-helix transcription factor TCF4 impacts brain architecture as well as neuronal morphology and differentiation.
PRISM: A Progenitor-Restricted Intersectional Fate Mapping Approach Redefines Forebrain Lineages.
Large-Area Fluorescence and Electron Microscopic Correlative Imaging With Multibeam Scanning Electron Microscopy.
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.
A trap mutant reveals the physiological client spectrum of TRC40.
Upregulated Expression of CUX1 Correlates with Poor Prognosis in Glioma Patients: a Bioinformatic Analysis.
Loss of homeoprotein Msx1 and Msx2 leading to athletic and kinematic impairment related to the increasing neural excitability of neurons in aberrant neocortex in mice.
Inactivating CUX1 mutations promote tumorigenesis.
Quantitative proteomic and genetic analyses of the schizophrenia susceptibility factor dysbindin identify novel roles of the biogenesis of lysosome-related organelles complex 1.
Li Y, An X, Mulcahey PJ, Qian Y, Xu XH, Zhao S, Mohan H, Suryanarayana SM, Bachschmid-Romano L, Brunel N, Whishaw IQ, Huang ZJ
bioRxiv : the preprint server for biology 2024 Oct 30;
bioRxiv : the preprint server for biology 2024 Oct 30;
BRN1/2 Function in Neocortical Size Determination and Microcephaly.
Barão S, Xu Y, Llongueras JP, Vistein R, Goff L, Nielsen K, Bae BI, Smith RS, Walsh CA, Stein-O'Brien G, Müller U
bioRxiv : the preprint server for biology 2024 May 15;
bioRxiv : the preprint server for biology 2024 May 15;
Cell type specific roles of FOXP1 during early neocortical murine development.
Ortiz A, Ayhan F, Harper M, Konopka G
bioRxiv : the preprint server for biology 2024 Jun 8;
bioRxiv : the preprint server for biology 2024 Jun 8;
iPSC-derived models of PACS1 syndrome reveal transcriptional and functional deficits in neuron activity.
Rylaarsdam L, Rakotomamonjy J, Pope E, Guemez-Gamboa A
Nature communications 2024 Jan 27;15(1):827
Nature communications 2024 Jan 27;15(1):827
A C-terminal motif containing a PKC phosphorylation site regulates γ-Protocadherin-mediated dendrite arborization in the cerebral cortex in vivo.
Hanes CM, Mah KM, Steffen DM, Marcucci CG, Fuller LC, Burgess RW, Garrett AM, Weiner JA
bioRxiv : the preprint server for biology 2024 Jan 25;
bioRxiv : the preprint server for biology 2024 Jan 25;
Disruption of lysosomal nutrient sensing scaffold contributes to pathogenesis of a fatal neurodegenerative lysosomal storage disease.
Bagh MB, Appu AP, Sadhukhan T, Mondal A, Plavelil N, Raghavankutty M, Supran AM, Sadhukhan S, Liu A, Mukherjee AB
The Journal of biological chemistry 2024 Feb;300(2):105641
The Journal of biological chemistry 2024 Feb;300(2):105641
Neonatal brain injury unravels transcriptional and signaling changes underlying the reactivation of cortical progenitors.
Foucault L, Capeliez T, Angonin D, Lentini C, Bezin L, Heinrich C, Parras C, Donega V, Marcy G, Raineteau O
Cell reports 2024 Feb 27;43(2):113734
Cell reports 2024 Feb 27;43(2):113734
The GDNF-gel/HA-Mg conduit promotes the repair of peripheral nerve defects by regulating PPAR-γ/RhoA/ROCK signaling pathway.
Cai Y, Chen Y, Zhang G, Lin Y, Zhang J, Liang J, Lv L, Wang Y, Fang X, Dang X
iScience 2024 Feb 16;27(2):108969
iScience 2024 Feb 16;27(2):108969
Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model.
Yuan Y, Lopez-Santiago L, Denomme N, Chen C, O'Malley HA, Hodges SL, Ji S, Han Z, Christiansen A, Isom LL
Brain : a journal of neurology 2024 Apr 4;147(4):1231-1246
Brain : a journal of neurology 2024 Apr 4;147(4):1231-1246
P53 independent pathogenic mechanisms contribute to BubR1 microcephaly.
Sterling NA, Terry BK, McDonnell JM, Kim S
Frontiers in cell and developmental biology 2023;11:1282182
Frontiers in cell and developmental biology 2023;11:1282182
Taok1 haploinsufficiency leads to autistic-like behaviors in mice via the dorsal raphe nucleus.
Wang J, Li W, Li Z, Xue Z, Zhang Y, Yuan Y, Shi Y, Shan S, Han W, Li F, Qiu Z
Cell reports 2023 Sep 26;42(9):113078
Cell reports 2023 Sep 26;42(9):113078
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.
Oppermann H, Marcos-Grañeda E, Weiss LA, Gurnett CA, Jelsig AM, Vineke SH, Isidor B, Mercier S, Magnussen K, Zacher P, Hashim M, Pagnamenta AT, Race S, Srivastava S, Frazier Z, Maiwald R, Pergande M, Milani D, Rinelli M, Levy J, Krey I, Fontana P, Lonardo F, Riley S, Kretzer J, Rankin J, Reis LM, Semina EV, Reuter MS, Scherer SW, Iascone M, Weis D, Fagerberg CR, Brasch-Andersen C, Hansen LK, Kuechler A, Noble N, Gardham A, Tenney J, Rathore G, Beck-Woedl S, Haack TB, Pavlidou DC, Atallah I, Vodopiutz J, Janecke AR, Hsieh TC, Lesmann H, Klinkhammer H, Krawitz PM, Lemke JR, Jamra RA, Nieto M, Tümer Z, Platzer K
European journal of human genetics : EJHG 2023 Nov;31(11):1251-1260
European journal of human genetics : EJHG 2023 Nov;31(11):1251-1260
Pituitary adenylate cyclase-activating polypeptide deficient mice show length abnormalities of the axon initial segment.
Iwahashi M, Yoshimura T, Harigai W, Takuma K, Hashimoto H, Katayama T, Hayata-Takano A
Journal of pharmacological sciences 2023 Nov;153(3):175-182
Journal of pharmacological sciences 2023 Nov;153(3):175-182
Stem cell competition driven by the Axin2-p53 axis controls brain size during murine development.
Sun XL, Chen ZH, Guo X, Wang J, Ge M, Wong SZH, Wang T, Li S, Yao M, Johnston LA, Wu QF
Developmental cell 2023 May 8;58(9):744-759.e11
Developmental cell 2023 May 8;58(9):744-759.e11
Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder.
Gandhi T, Canepa CR, Adeyelu TT, Adeniyi PA, Lee CC
Brain sciences 2023 May 31;13(6)
Brain sciences 2023 May 31;13(6)
Notch directs telencephalic development and controls neocortical neuron fate determination by regulating microRNA levels.
Han JS, Fishman-Williams E, Decker SC, Hino K, Reyes RV, Brown NL, Simó S, Torre A
Development (Cambridge, England) 2023 Jun 1;150(11)
Development (Cambridge, England) 2023 Jun 1;150(11)
A Robust Pipeline for the Multi-Stage Accelerated Differentiation of Functional 3D Cortical Organoids from Human Pluripotent Stem Cells.
Whye D, Wood D, Saber WA, Norabuena EM, Makhortova NR, Sahin M, Buttermore ED
Current protocols 2023 Jan;3(1):e641
Current protocols 2023 Jan;3(1):e641
An entosis-like process induces mitotic disruption in Pals1 microcephaly pathogenesis.
Sterling NA, Park JY, Park R, Cho SH, Kim S
Nature communications 2023 Jan 5;14(1):82
Nature communications 2023 Jan 5;14(1):82
Effect of CUX1 on the Proliferation of Hu Sheep Dermal Papilla Cells and on the Wnt/β-Catenin Signaling Pathway.
Zhou H, Huang S, Lv X, Wang S, Cao X, Yuan Z, Getachew T, Mwacharo JM, Haile A, Quan K, Li Y, Reverter A, Sun W
Genes 2023 Feb 7;14(2)
Genes 2023 Feb 7;14(2)
RNA methylation-related genes of m6A, m5C, and m1A predict prognosis and immunotherapy response in cervical cancer.
Wang Y, Mao Y, Wang C, Jiang X, Tang Q, Wang L, Zhu J, Zhao M
Annals of medicine 2023 Dec;55(1):2190618
Annals of medicine 2023 Dec;55(1):2190618
An adhesion signaling axis involving Dystroglycan, β1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold.
Wong W, Estep JA, Treptow AM, Rajabli N, Jahncke JN, Ubina T, Wright KM, Riccomagno MM
PLoS biology 2023 Aug;21(8):e3002212
PLoS biology 2023 Aug;21(8):e3002212
Npas3 regulates stemness maintenance of radial glial cells and neuronal migration in the developing mouse cerebral cortex.
Liu JW, Li H, Zhang Y
Frontiers in cellular neuroscience 2022;16:865681
Frontiers in cellular neuroscience 2022;16:865681
Astrocytic Piezo1-mediated mechanotransduction determines adult neurogenesis and cognitive functions.
Chi S, Cui Y, Wang H, Jiang J, Zhang T, Sun S, Zhou Z, Zhong Y, Xiao B
Neuron 2022 Sep 21;110(18):2984-2999.e8
Neuron 2022 Sep 21;110(18):2984-2999.e8
Increased glycine contributes to synaptic dysfunction and early mortality in Nprl2 seizure model.
Dentel B, Angeles-Perez L, Ren C, Jakkamsetti V, Holley AJ, Caballero D, Oh E, Gibson J, Pascual JM, Huber KM, Tu BP, Tsai PT
iScience 2022 May 20;25(5):104334
iScience 2022 May 20;25(5):104334
TMEM106B deficiency impairs cerebellar myelination and synaptic integrity with Purkinje cell loss.
Feng T, Luan L, Katz II, Ullah M, Van Deerlin VM, Trojanowski JQ, Lee EB, Hu F
Acta neuropathologica communications 2022 Mar 14;10(1):33
Acta neuropathologica communications 2022 Mar 14;10(1):33
Divergent transcriptional regulation of astrocyte reactivity across disorders.
Burda JE, O'Shea TM, Ao Y, Suresh KB, Wang S, Bernstein AM, Chandra A, Deverasetty S, Kawaguchi R, Kim JH, McCallum S, Rogers A, Wahane S, Sofroniew MV
Nature 2022 Jun;606(7914):557-564
Nature 2022 Jun;606(7914):557-564
CUX1 promotes epithelial-mesenchymal transition (EMT) in renal fibrosis of UUO model by targeting MMP7.
Teng S, Liu G, Li L, Ou J, Yu Y
Biochemical and biophysical research communications 2022 Jun 11;608:128-134
Biochemical and biophysical research communications 2022 Jun 11;608:128-134
Post-GWAS functional analysis identifies CUX1 as a regulator of p16(INK4a) and cellular senescence.
Jiang D, Sun W, Wu T, Zou M, Vasamsetti SB, Zhang X, Zhao Y, Phillippi JA, Sawalha AH, Tavakoli S, Dutta P, Florentin J, Chan SY, Tollison TS, Di Wu, Cui J, Huntress I, Peng X, Finkel T, Li G
Nature aging 2022 Feb;2(2):140-154
Nature aging 2022 Feb;2(2):140-154
Length impairments of the axon initial segment in rodent models of attention-deficit hyperactivity disorder and autism spectrum disorder.
Usui N, Tian X, Harigai W, Togawa S, Utsunomiya R, Doi T, Miyoshi K, Shinoda K, Tanaka J, Shimada S, Katayama T, Yoshimura T
Neurochemistry international 2022 Feb;153:105273
Neurochemistry international 2022 Feb;153:105273
Merkel cell polyomavirus small T antigen is a viral transcription activator that is essential for viral genome maintenance.
Rapchak K, Yagobian SD, Moore J, Khattri M, Shuda M
PLoS pathogens 2022 Dec;18(12):e1011039
PLoS pathogens 2022 Dec;18(12):e1011039
GRN-/- iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosis.
Bossolasco P, Cimini S, Maderna E, Bardelli D, Canafoglia L, Cavallaro T, Ricci M, Silani V, Marucci G, Rossi G
Neurobiology of disease 2022 Dec;175:105891
Neurobiology of disease 2022 Dec;175:105891
Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.
Wang S, Wu T, Sun J, Li Y, Yuan Z, Sun W
Frontiers in cell and developmental biology 2021;9:800157
Frontiers in cell and developmental biology 2021;9:800157
Restoration of Visual Function and Cortical Connectivity After Ischemic Injury Through NeuroD1-Mediated Gene Therapy.
Tang Y, Wu Q, Gao M, Ryu E, Pei Z, Kissinger ST, Chen Y, Rao AK, Xiang Z, Wang T, Li W, Chen G, Chubykin AA
Frontiers in cell and developmental biology 2021;9:720078
Frontiers in cell and developmental biology 2021;9:720078
CUX1 Facilitates the Development of Oncogenic Properties Via Activating Wnt/β-Catenin Signaling Pathway in Glioma.
Feng F, Zhao Z, Zhou Y, Cheng Y, Wu X, Heng X
Frontiers in molecular biosciences 2021;8:705008
Frontiers in molecular biosciences 2021;8:705008
Neuroserpin Is Strongly Expressed in the Developing and Adult Mouse Neocortex but Its Absence Does Not Perturb Cortical Lamination and Synaptic Proteome.
Kement D, Reumann R, Schostak K, Voß H, Douceau S, Dottermusch M, Schweizer M, Schlüter H, Vivien D, Glatzel M, Galliciotti G
Frontiers in neuroanatomy 2021;15:627896
Frontiers in neuroanatomy 2021;15:627896
RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity.
Proietti Onori M, Koene LMC, Schäfer CB, Nellist M, de Brito van Velze M, Gao Z, Elgersma Y, van Woerden GM
PLoS biology 2021 May;19(5):e3001279
PLoS biology 2021 May;19(5):e3001279
IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype.
Hayano Y, Ishino Y, Hyun JH, Orozco CG, Steinecke A, Potts E, Oisi Y, Thomas CI, Guerrero-Given D, Kim E, Kwon HB, Kamasawa N, Taniguchi H
Science advances 2021 Jul;7(29)
Science advances 2021 Jul;7(29)
Cellular and Behavioral Characterization of Pcdh19 Mutant Mice: subtle Molecular Changes, Increased Exploratory Behavior and an Impact of Social Environment.
Galindo-Riera N, Newbold SA, Sledziowska M, Llinares-Benadero C, Griffiths J, Mire E, Martinez-Garay I
eNeuro 2021 Jul-Aug;8(4)
eNeuro 2021 Jul-Aug;8(4)
Centrosome defects cause microcephaly by activating the 53BP1-USP28-TP53 mitotic surveillance pathway.
Phan TP, Maryniak AL, Boatwright CA, Lee J, Atkins A, Tijhuis A, Spierings DC, Bazzi H, Foijer F, Jordan PW, Stracker TH, Holland AJ
The EMBO journal 2021 Jan 4;40(1):e106118
The EMBO journal 2021 Jan 4;40(1):e106118
Overexpressed P75CUX1 promotes EMT in glioma infiltration by activating β-catenin.
Xu A, Wang X, Luo J, Zhou M, Yi R, Huang T, Lin J, Wu Z, Xie C, Ding S, Zeng Y, Song Y
Cell death & disease 2021 Feb 4;12(2):157
Cell death & disease 2021 Feb 4;12(2):157
Astragalus polysaccharide regulates brown adipogenic differentiation through miR-1258-5p-modulated cut-like homeobox 1 expression.
Cao Y, Deng B, Zhang S, Gao H, Song P, Zhang J, Zhao J
Acta biochimica et biophysica Sinica 2021 Dec 8;53(12):1713-1722
Acta biochimica et biophysica Sinica 2021 Dec 8;53(12):1713-1722
miR-143 Targeting CUX1 to Regulate Proliferation of Dermal Papilla Cells in Hu Sheep.
Hu T, Huang S, Lv X, Wang S, Getachew T, Mwacharo JM, Haile A, Sun W
Genes 2021 Dec 18;12(12)
Genes 2021 Dec 18;12(12)
Differential Expression Levels of Sox9 in Early Neocortical Radial Glial Cells Regulate the Decision between Stem Cell Maintenance and Differentiation.
Fabra-Beser J, Alves Medeiros de Araujo J, Marques-Coelho D, Goff LA, Costa MR, Müller U, Gil-Sanz C
The Journal of neuroscience : the official journal of the Society for Neuroscience 2021 Aug 18;41(33):6969-6986
The Journal of neuroscience : the official journal of the Society for Neuroscience 2021 Aug 18;41(33):6969-6986
ZBTB20 is crucial for the specification of a subset of callosal projection neurons and astrocytes in the mammalian neocortex.
Medeiros de Araújo JA, Barão S, Mateos-White I, Espinosa A, Costa MR, Gil-Sanz C, Müller U
Development (Cambridge, England) 2021 Aug 15;148(16)
Development (Cambridge, England) 2021 Aug 15;148(16)
Cut-like homeobox 1 (CUX1) tumor suppressor gene haploinsufficiency induces apoptosis evasion to sustain myeloid leukemia.
Supper E, Rudat S, Iyer V, Droop A, Wong K, Spinella JF, Thomas P, Sauvageau G, Adams DJ, Wong CC
Nature communications 2021 Apr 30;12(1):2482
Nature communications 2021 Apr 30;12(1):2482
AIF3 splicing switch triggers neurodegeneration.
Liu S, Zhou M, Ruan Z, Wang Y, Chang C, Sasaki M, Rajaram V, Lemoff A, Nambiar K, Wang JE, Hatanpaa KJ, Luo W, Dawson TM, Dawson VL, Wang Y
Molecular neurodegeneration 2021 Apr 14;16(1):25
Molecular neurodegeneration 2021 Apr 14;16(1):25
Liquid Biopsy of Extracellular Vesicle-Derived miR-193a-5p in Colorectal Cancer and Discovery of Its Tumor-Suppressor Functions.
Wei R, Chen L, Qin D, Guo Q, Zhu S, Li P, Min L, Zhang S
Frontiers in oncology 2020;10:1372
Frontiers in oncology 2020;10:1372
hGFAP-Positive Stem Cells Depend on Brg1 for Proper Formation of Cerebral and Cerebellar Structures.
Holdhof D, Schoof M, Hellwig M, Holdhof NH, Niesen J, Schüller U
Cerebral cortex (New York, N.Y. : 1991) 2020 Mar 14;30(3):1382-1392
Cerebral cortex (New York, N.Y. : 1991) 2020 Mar 14;30(3):1382-1392
Reversing a model of Parkinson's disease with in situ converted nigral neurons.
Qian H, Kang X, Hu J, Zhang D, Liang Z, Meng F, Zhang X, Xue Y, Maimon R, Dowdy SF, Devaraj NK, Zhou Z, Mobley WC, Cleveland DW, Fu XD
Nature 2020 Jun;582(7813):550-556
Nature 2020 Jun;582(7813):550-556
The basic helix-loop-helix transcription factor TCF4 impacts brain architecture as well as neuronal morphology and differentiation.
Schoof M, Hellwig M, Harrison L, Holdhof D, Lauffer MC, Niesen J, Virdi S, Indenbirken D, Schüller U
The European journal of neuroscience 2020 Jun;51(11):2219-2235
The European journal of neuroscience 2020 Jun;51(11):2219-2235
PRISM: A Progenitor-Restricted Intersectional Fate Mapping Approach Redefines Forebrain Lineages.
Poulin JF, Luppi MP, Hofer C, Caronia G, Hsu PK, Chan CS, Awatramani R
Developmental cell 2020 Jun 22;53(6):740-753.e3
Developmental cell 2020 Jun 22;53(6):740-753.e3
Large-Area Fluorescence and Electron Microscopic Correlative Imaging With Multibeam Scanning Electron Microscopy.
Shibata S, Iseda T, Mitsuhashi T, Oka A, Shindo T, Moritoki N, Nagai T, Otsubo S, Inoue T, Sasaki E, Akazawa C, Takahashi T, Schalek R, Lichtman JW, Okano H
Frontiers in neural circuits 2019;13:29
Frontiers in neural circuits 2019;13:29
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.
Ivanova EL, Gilet JG, Sulimenko V, Duchon A, Rudolf G, Runge K, Collins SC, Asselin L, Broix L, Drouot N, Tilly P, Nusbaum P, Vincent A, Magnant W, Skory V, Birling MC, Pavlovic G, Godin JD, Yalcin B, Hérault Y, Dráber P, Chelly J, Hinckelmann MV
Nature communications 2019 May 13;10(1):2129
Nature communications 2019 May 13;10(1):2129
A trap mutant reveals the physiological client spectrum of TRC40.
Coy-Vergara J, Rivera-Monroy J, Urlaub H, Lenz C, Schwappach B
Journal of cell science 2019 Jul 1;132(13)
Journal of cell science 2019 Jul 1;132(13)
Upregulated Expression of CUX1 Correlates with Poor Prognosis in Glioma Patients: a Bioinformatic Analysis.
Wu X, Feng F, Yang C, Zhang M, Cheng Y, Zhao Y, Wang Y, Che F, Zhang J, Heng X
Journal of molecular neuroscience : MN 2019 Dec;69(4):527-537
Journal of molecular neuroscience : MN 2019 Dec;69(4):527-537
Loss of homeoprotein Msx1 and Msx2 leading to athletic and kinematic impairment related to the increasing neural excitability of neurons in aberrant neocortex in mice.
Yu B, Jin Y, Shen Y, Yang Y, Wang G, Zhu H, Yu Y, Wang J
Biochemical and biophysical research communications 2019 Aug 13;516(1):229-235
Biochemical and biophysical research communications 2019 Aug 13;516(1):229-235
Inactivating CUX1 mutations promote tumorigenesis.
Wong CC, Martincorena I, Rust AG, Rashid M, Alifrangis C, Alexandrov LB, Tiffen JC, Kober C, Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium, Green AR, Massie CE, Nangalia J, Lempidaki S, Döhner H, Döhner K, Bray SJ, McDermott U, Papaemmanuil E, Campbell PJ, Adams DJ
Nature genetics 2014 Jan;46(1):33-8
Nature genetics 2014 Jan;46(1):33-8
Quantitative proteomic and genetic analyses of the schizophrenia susceptibility factor dysbindin identify novel roles of the biogenesis of lysosome-related organelles complex 1.
Gokhale A, Larimore J, Werner E, So L, Moreno-De-Luca A, Lese-Martin C, Lupashin VV, Smith Y, Faundez V
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 Mar 14;32(11):3697-711
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 Mar 14;32(11):3697-711
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Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- human brain tissue were subjected to SDS PAGE followed by western blot with 11733-1-AP(CUX1 antibody) at dilution of 1:2000
- Sample type
- tissue
Supportive validation
- Submitted by
- Proteintech Group (provider)
- Main image
- Experimental details
- Immunofluorescent analysis of HepG2 cells, using CUX1 antibody 11733-1-AP at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red).
- Sample type
- cell line