| scholarly article | Q13442814 |
| P50 | author | John Ngai | Q93005267 |
| P2093 | author name string | Cheryl Y Gregory-Evans | |
| Ishaq A Viringipurampeer | |||
| Kevin Gregory-Evans | |||
| Jookyung J Yoon | |||
| Mariya Moosajee | |||
| Shannon DeMaria | |||
| Todd Ferreira | |||
| Xianghong Shan | |||
| P2860 | cites work | p53 activation by knockdown technologies | Q21563456 |
| A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis | Q22010374 | ||
| Cleavage of the death domain kinase RIP by caspase-8 prompts TNF-induced apoptosis | Q22010649 | ||
| FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis | Q24307362 | ||
| Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies | Q24311933 | ||
| WNT5A is regulated by PAX2 and may be involved in blastemal predominant Wilms tumorigenesis | Q24320196 | ||
| Fbxl10/Kdm2b deficiency accelerates neural progenitor cell death and leads to exencephaly | Q24336380 | ||
| Phosphorylation-driven assembly of the RIP1-RIP3 complex regulates programmed necrosis and virus-induced inflammation | Q24338129 | ||
| Neuronal apoptosis inhibitory protein is expressed in developing kidney and is regulated by PAX2 | Q24338358 | ||
| Heterozygous mutations of OTX2 cause severe ocular malformations | Q24530768 | ||
| Vax1, a novel homeobox-containing gene, directs development of the basal forebrain and visual system | Q24596773 | ||
| The Fas-associated death domain protein is required in apoptosis and TLR-induced proliferative responses in B cells | Q24621785 | ||
| GDF6, a novel locus for a spectrum of ocular developmental anomalies | Q24680270 | ||
| FADD: an endogenous inhibitor of RIP3-driven regulated necrosis | Q26823535 | ||
| Stages of embryonic development of the zebrafish | Q27860947 | ||
| Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse | Q28212459 | ||
| SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma | Q28237882 | ||
| FADD: essential for embryo development and signaling from some, but not all, inducers of apoptosis | Q28265012 | ||
| Fas-mediated apoptosis and activation-induced T-cell proliferation are defective in mice lacking FADD/Mort1 | Q28265912 | ||
| FADD: a regulator of life and death | Q28286149 | ||
| In situ detection of fragmented DNA (TUNEL assay) fails to discriminate among apoptosis, necrosis, and autolytic cell death: a cautionary note | Q28300836 | ||
| Pax2 contributes to inner ear patterning and optic nerve trajectory | Q28511597 | ||
| Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes | Q28586361 | ||
| Mechanisms of necroptosis in T cells | Q28592588 | ||
| A series of no isthmus (noi) alleles of the zebrafish pax2.1 gene reveals multiple signaling events in development of the midbrain-hindbrain boundary | Q47073721 | ||
| Mutations affecting development of the notochord in zebrafish | Q47073736 | ||
| Impaired retinal differentiation and maintenance in zebrafish laminin mutants | Q47073779 | ||
| Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain | Q47073829 | ||
| Zebrafish mutants identify an essential role for laminins in notochord formation. | Q48297604 | ||
| The Pax protein Noi is required for commissural axon pathway formation in the rostral forebrain | Q48694650 | ||
| Differential activation of phospholipases during necrosis or apoptosis: a comparative study using tumor necrosis factor and anti-Fas antibodies | Q49171557 | ||
| Identification of starmaker-like in medaka as a putative target gene of Pax2 in the otic vesicle. | Q50442296 | ||
| Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21. | Q52087373 | ||
| Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT). | Q52166624 | ||
| Is programmed cell death required for neural tube closure? | Q52195654 | ||
| Identification of RAPD primers that reveal extensive polymorphisms between laboratory strains of zebrafish. | Q52219588 | ||
| DNA sequence recognition by Pax proteins: bipartite structure of the paired domain and its binding site. | Q52222420 | ||
| FADD prevents RIP3-mediated epithelial cell necrosis and chronic intestinal inflammation. | Q52614520 | ||
| Novel SOX2 mutation associated with ocular coloboma in a Chinese family | Q81262743 | ||
| RIP3, an energy metabolism regulator that switches TNF-induced cell death from apoptosis to necrosis | Q28594624 | ||
| In situ detection of fragmented dna (tunel assay) fails to discriminate among apoptosis, necrosis, and autolytic cell death: A cautionary note | Q29026600 | ||
| Effective targeted gene 'knockdown' in zebrafish | Q29547445 | ||
| Identification of RIP1 kinase as a specific cellular target of necrostatins | Q29616006 | ||
| RIP3 mediates the embryonic lethality of caspase-8-deficient mice | Q29617723 | ||
| Stage-specific expression of TNFα regulates bad/bid-mediated apoptosis and RIP1/ROS-mediated secondary necrosis in Birnavirus-infected fish cells | Q33815339 | ||
| Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma | Q33838251 | ||
| Caspase-8 regulates TNF-α-induced epithelial necroptosis and terminal ileitis. | Q34216810 | ||
| Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. | Q34314263 | ||
| Identification of Pax2-regulated genes by expression profiling of the mid-hindbrain organizer region | Q34416114 | ||
| Functional complementation between FADD and RIP1 in embryos and lymphocytes | Q34768810 | ||
| Epithelial fusions in the embryo | Q34858163 | ||
| Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators | Q34876963 | ||
| Gene-specific differential response to anti-apoptotic therapies in zebrafish models of ocular coloboma. | Q35032282 | ||
| Ocular coloboma: a reassessment in the age of molecular neuroscience | Q35444452 | ||
| Synergistic protective effects of humanin and necrostatin-1 on hypoxia and ischemia/reperfusion injury | Q36141885 | ||
| Sequence alterations in RX in patients with microphthalmia, anophthalmia, and coloboma | Q37066070 | ||
| A transcriptionally silent RXRalpha supports early embryonic morphogenesis and heart development | Q37132891 | ||
| Apoptosis is not required for mammalian neural tube closure. | Q37208642 | ||
| Foxg1 is required for development of the vertebrate olfactory system | Q37251212 | ||
| A gain-of-function screen in zebrafish identifies a guanylate cyclase with a role in neuronal degeneration | Q37270525 | ||
| Fish'n ChIPs: chromatin immunoprecipitation in the zebrafish embryo | Q37545577 | ||
| Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database. | Q37972823 | ||
| Identification of a Pax paired domain recognition sequence and evidence for DNA-dependent conformational changes | Q38310017 | ||
| Impossibility of acridine orange intercalation in nuclear DNA of the living cell | Q39254703 | ||
| Apoptosis and necroptosis are induced in rainbow trout cell lines exposed to cadmium. | Q39708457 | ||
| Necroptosis, necrosis and secondary necrosis converge on similar cellular disintegration features. | Q39763280 | ||
| Necrostatin: a potentially novel cardioprotective agent? | Q40100232 | ||
| Cleavage of RIP3 inactivates its caspase-independent apoptosis pathway by removal of kinase domain. | Q40103903 | ||
| The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype | Q41301123 | ||
| Characterization of zebrafish caspase-3 and induction of apoptosis through ceramide generation in fish fathead minnow tailbud cells and zebrafish embryo | Q42157819 | ||
| FADD deficiency impairs early hematopoiesis in the bone marrow | Q42224191 | ||
| Analysis of beta cell proliferation dynamics in zebrafish. | Q42798572 | ||
| Mutations in N-cadherin and a Stardust homolog, Nagie oko, affect cell-cycle exit in zebrafish retina | Q43110712 | ||
| Necroptosis, a novel form of caspase-independent cell death, contributes to neuronal damage in a retinal ischemia-reperfusion injury model | Q43213260 | ||
| 2001 Warkany lecture: to die or not to die, the role of apoptosis in normal and abnormal mammalian development | Q43424410 | ||
| Hedgehog signalling maintains the optic stalk-retinal interface through the regulation of Vax gene activity | Q44285295 | ||
| N-cadherin mediates retinal lamination, maintenance of forebrain compartments and patterning of retinal neurites | Q44408459 | ||
| Tumor necrosis factor-induced nonapoptotic cell death requires receptor-interacting protein-mediated cellular reactive oxygen species accumulation | Q44710589 | ||
| Translational bypass of nonsense mutations in zebrafish rep1, pax2.1 and lamb1 highlights a viable therapeutic option for untreatable genetic eye disease | Q46352595 | ||
| Necroptosis contributes to the NMDA-induced excitotoxicity in rat's cultured cortical neurons | Q46414173 | ||
| P433 | issue | 10 | |
| P304 | page(s) | 2357-2369 | |
| P577 | publication date | 2012-02-21 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Pax2 regulates a fadd-dependent molecular switch that drives tissue fusion during eye development | |
| P478 | volume | 21 |
| Q37078872 | Bcl6a function is required during optic cup formation to prevent p53-dependent apoptosis and colobomata |
| Q38517281 | Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma |
| Q90382743 | FADD in Cancer: Mechanisms of Altered Expression and Function, and Clinical Implications |
| Q51044275 | Frizzled 3 acts upstream of Alcam during embryonic eye development. |
| Q96640025 | Hyaloid vasculature and mmp2 activity play a role during optic fissure fusion in zebrafish |
| Q27334126 | Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis. |
| Q89919423 | Mutation in Bmpr1b Leads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice |
| Q24319044 | Mutation of SALL2 causes recessive ocular coloboma in humans and mice |
| Q35125578 | Mutations in MAB21L2 result in ocular Coloboma, microcornea and cataracts |
| Q41865714 | Negative and positive auto-regulation of BMP expression in early eye development |
| Q34473649 | Otx2 is involved in the regional specification of the developing retinal pigment epithelium by preventing the expression of sox2 and fgf8, factors that induce neural retina differentiation |
| Q36414959 | Priorities and trends in the study of proteins in eye research, 1924-2014 |
| Q38641936 | Rip3 knockdown rescues photoreceptor cell death in blind pde6c zebrafish |
| Q38822858 | The zebrafish eye-a paradigm for investigating human ocular genetics. |
| Q91630796 | Zebrafish mab21l2 mutants possess severe defects in optic cup morphogenesis, lens and cornea development |
| Q97538301 | dnmt1 function is required to maintain retinal stem cells within the ciliary marginal zone of the zebrafish eye |
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