scholarly article | Q13442814 |
P2093 | author name string | Pierre-Olivier Frappart | |
Anielle L Gomes | |||
Gabriel E Matos-Rodrigues | |||
Rodrigo A P Martins | |||
P2860 | cites work | RINT-1, a novel Rad50-interacting protein, participates in radiation-induced G(2)/M checkpoint control | Q24290563 |
RINT-1 regulates the localization and entry of ZW10 to the syntaxin 18 complex | Q24311852 | ||
Implication of ZW10 in membrane trafficking between the endoplasmic reticulum and Golgi | Q24317648 | ||
Chk1 is an essential kinase that is regulated by Atr and required for the G(2)/M DNA damage checkpoint | Q24604730 | ||
The DNA-damage response in human biology and disease | Q24606586 | ||
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009 | Q24653924 | ||
RINT-1 serves as a tumor suppressor and maintains Golgi dynamics and centrosome integrity for cell survival | Q24675915 | ||
Moonlighting functions of the NRZ (mammalian Dsl1) complex | Q26825961 | ||
Math5 is required for retinal ganglion cell and optic nerve formation | Q28345639 | ||
Requirement for math5 in the development of retinal ganglion cells | Q28345916 | ||
Math5 determines the competence state of retinal ganglion cell progenitors | Q28506349 | ||
An essential function for NBS1 in the prevention of ataxia and cerebellar defects | Q28507300 | ||
Defective neurogenesis resulting from DNA ligase IV deficiency requires Atm | Q28510231 | ||
Ocular Anomalies in Seckel's Syndrome | Q69040073 | ||
A P53-Independent DNA Damage Response Suppresses Oncogenic Proliferation and Genome Instability | Q89548697 | ||
The Role of Autophagy in Glaucomatous Optic Neuropathy | Q90643285 | ||
An intrinsic S/G2 checkpoint enforced by ATR | Q91113594 | ||
DNA double-strand break repair-pathway choice in somatic mammalian cells | Q91529889 | ||
RAG-2 deficiency results in fewer phosphorylated histone H2AX foci, but increased retinal ganglion cell death and altered axonal growth | Q91767877 | ||
The multiple mechanisms that regulate p53 activity and cell fate | Q92062954 | ||
De novo genesis of retinal ganglion cells by targeted expression of Klf4 in vivo | Q92576583 | ||
Neurogenesis and Specification of Retinal Ganglion Cells | Q92637310 | ||
RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities | Q92780373 | ||
Aneuploid acute myeloid leukemia exhibits a signature of genomic alterations in the cell cycle and protein degradation machinery | Q93336562 | ||
Conditional inactivation of the NBS1 gene in the mouse central nervous system leads to neurodegeneration and disorganization of the visual system | Q41938037 | ||
Bloom syndrome: multiple retinopathies in a chromosome breakage disorder | Q42219871 | ||
DNA-PK promotes the survival of young neurons in the embryonic mouse retina | Q43071286 | ||
Retinal Features in Seckel's Syndrome | Q44618676 | ||
Radiation-induced apoptosis in developing mouse retina exhibits dose-dependent requirement for ATM phosphorylation of p53. | Q44749119 | ||
Timing and topography of cell genesis in the rat retina | Q44911589 | ||
Cell differentiation in the retina of the mouse | Q45193462 | ||
Congenital hypertrophy of retinal pigment epithelium in non-Gardner's polyposis kindreds | Q45879873 | ||
Genome integrity and disease prevention in the nervous system | Q47148140 | ||
Characterization of the phenotype and birthdates of pyknotic dead cells in the nervous system by a combination of DNA staining and immunohistochemistry for 5'-bromodeoxyuridine and neural antigens | Q48277761 | ||
The early development of the optic nerve and chiasm in embryonic rat. | Q48385159 | ||
Synergistic tumor suppressor activity of BRCA2 and p53 in a conditional mouse model for breast cancer. | Q52544495 | ||
Bilateral retinal detachment in Seckel syndrome. | Q52873379 | ||
BRCA2 function and the central nervous system. | Q53530318 | ||
The MRE11-RAD50-NBS1 Complex Conducts the Orchestration of Damage Signaling and Outcomes to Stress in DNA Replication and Repair. | Q54980026 | ||
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families | Q64075131 | ||
The intersection between DNA damage response and cell death pathways | Q28611423 | ||
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers | Q28652056 | ||
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data | Q29616810 | ||
The intersection of Golgi-ER retrograde and autophagic trafficking | Q33357109 | ||
Retinal vasculopathy in Fanconi anemia | Q33505745 | ||
A p53-independent role for the MDM2 antagonist Nutlin-3 in DNA damage response initiation | Q33825730 | ||
The MRN complex in double-strand break repair and telomere maintenance | Q34127693 | ||
Regulating proliferation during retinal development | Q34238084 | ||
The p53 network: cellular and systemic DNA damage responses in aging and cancer | Q34248711 | ||
Requirement for Atm in ionizing radiation-induced cell death in the developing central nervous system | Q34467644 | ||
The Rb-related p130 protein controls telomere lengthening through an interaction with a Rad50-interacting protein, RINT-1. | Q34511522 | ||
Nbn and atm cooperate in a tissue and developmental stage-specific manner to prevent double strand breaks and apoptosis in developing brain and eye. | Q34919494 | ||
From progenitors to differentiated cells in the vertebrate retina | Q34990515 | ||
Neurogenesis and the Cell Cycle | Q35558404 | ||
Morphological features of cell death | Q35773151 | ||
Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle. | Q35914616 | ||
Cell Cycle Regulation and Apoptotic Responses of the Embryonic Chick Retina by Ionizing Radiation | Q36013224 | ||
Evaluation of Rint1 as a modifier of intestinal tumorigenesis and cancer risk | Q36298287 | ||
Integrative functional genomics identifies RINT1 as a novel GBM oncogene | Q36344771 | ||
Developmental abnormalities of the optic nerve and chiasm | Q36959882 | ||
Mouse models of DNA double-strand break repair and neurological disease | Q37155146 | ||
A new role for RINT-1 in SNARE complex assembly at the trans-Golgi network in coordination with the COG complex | Q37167924 | ||
The p53 family and programmed cell death | Q37310208 | ||
Rint1 inactivation triggers genomic instability, ER stress and autophagy inhibition in the brain. | Q37354009 | ||
The molecular basis of retinal ganglion cell death in glaucoma | Q37966513 | ||
Retinal neurogenesis | Q38175009 | ||
Bilateral retinal detachment in Werner syndrome | Q38265224 | ||
The essential kinase ATR: ensuring faithful duplication of a challenging genome. | Q38622938 | ||
N-myc regulates growth and fiber cell differentiation in lens development | Q38674970 | ||
RINT-1 interacts with MSP58 within nucleoli and plays a role in ribosomal gene transcription | Q38751504 | ||
Autophagy in the eye: Development, degeneration, and aging | Q38938383 | ||
A role for the MRN complex in ATR activation via TOPBP1 recruitment | Q39167332 | ||
ATR maintains chromosomal integrity during postnatal cerebellar neurogenesis and is required for medulloblastoma formation | Q39226312 | ||
Pax6 is required for the multipotent state of retinal progenitor cells | Q40813005 | ||
Birth dates of retinal ganglion cells giving rise to the crossed and uncrossed optic projections in the mouse | Q41387837 | ||
ATR maintains select progenitors during nervous system development | Q41767755 | ||
Neurogenesis requires TopBP1 to prevent catastrophic replicative DNA damage in early progenitors. | Q41826040 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P304 | page(s) | 711 | |
P577 | publication date | 2020-07-30 | |
P1433 | published in | Frontiers in Cell and Developmental Biology | Q27725488 |
P1476 | title | RINT1 Loss Impairs Retinogenesis Through TRP53-Mediated Apoptosis | |
P478 | volume | 8 |
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