{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T22:19:31Z","timestamp":1792016371318,"version":"4.4.0"},"reference-count":50,"publisher":"Elsevier BV","issue":"38","license":[{"start":{"date-parts":[[2019,9,1]],"date-time":"2019-09-01T00:00:00Z","timestamp":1567296000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,9,4]],"date-time":"2020-09-04T00:00:00Z","timestamp":1599177600000},"content-version":"vor","delay-in-days":369,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China (NSF)","doi-asserted-by":"publisher","award":["81800870"],"award-info":[{"award-number":["81800870"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China (NSF)","doi-asserted-by":"publisher","award":["31571303"],"award-info":[{"award-number":["31571303"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China (NSF)","doi-asserted-by":"publisher","award":["31801041"],"award-info":[{"award-number":["31801041"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China (NSF)","doi-asserted-by":"publisher","award":["81670890"],"award-info":[{"award-number":["81670890"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China (NSF)","doi-asserted-by":"publisher","award":["31871260"],"award-info":[{"award-number":["31871260"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["jbc.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Biological Chemistry"],"published-print":{"date-parts":[[2019,9]]},"DOI":"10.1074\/jbc.ra119.008618","type":"journal-article","created":{"date-parts":[[2019,7,30]],"date-time":"2019-07-30T17:45:10Z","timestamp":1564508710000},"page":"13953-13963","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":35,"title":["Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration"],"prefix":"10.1016","volume":"294","author":[{"given":"Zhaojing","family":"Lu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xuebin","family":"Hu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James","family":"Reilly","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Danna","family":"Jia","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0310-1072","authenticated-orcid":false,"given":"Fei","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shanshan","family":"Yu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiliang","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shanglun","family":"Xie","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhen","family":"Qu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yayun","family":"Qin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuwen","family":"Huang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuexia","family":"Lv","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jingzhen","family":"Li","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pan","family":"Gao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fulton","family":"Wong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xinhua","family":"Shu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhaohui","family":"Tang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mugen","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1074\/jbc.RA119.008618_bib1","doi-asserted-by":"crossref","first-page":"2297","DOI":"10.1523\/JNEUROSCI.2034-08.2009","article-title":"Loss of the cholesterol-binding protein prominin-1\/CD133 causes disk dysmorphogenesis and photoreceptor degeneration","volume":"29","author":"Zacchigna","year":"2009","journal-title":"J. Neurosci"},{"key":"10.1074\/jbc.RA119.008618_bib2","doi-asserted-by":"crossref","first-page":"5013","DOI":"10.1182\/blood.V90.12.5013","article-title":"A novel five-transmembrane hematopoietic stem cell antigen: isolation, characterization, and molecular cloning","volume":"90","author":"Miraglia","year":"1997","journal-title":"Blood"},{"key":"10.1074\/jbc.RA119.008618_bib3","doi-asserted-by":"crossref","first-page":"4301","DOI":"10.1242\/jcs.01315","article-title":"Identification of novel prominin-1\/CD133 splice variants with alternative C-termini and their expression in epididymis and testis","volume":"117","author":"Fargeas","year":"2004","journal-title":"J. Cell Sci"},{"key":"10.1074\/jbc.RA119.008618_bib4","doi-asserted-by":"crossref","first-page":"48","DOI":"10.1186\/1471-2407-8-48","article-title":"Expression of the \u201cstem cell marker\u201d CD133 in pancreas and pancreatic ductal adenocarcinomas","volume":"8","author":"Immervoll","year":"2008","journal-title":"BMC Cancer"},{"key":"10.1074\/jbc.RA119.008618_bib5","doi-asserted-by":"crossref","first-page":"1285","DOI":"10.1038\/sj.bjc.6604664","article-title":"CD133 expression is an independent prognostic marker for low survival in colorectal cancer","volume":"99","author":"Horst","year":"2008","journal-title":"Br. J. Cancer"},{"key":"10.1074\/jbc.RA119.008618_bib6","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1093\/hmg\/9.1.27","article-title":"A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration","volume":"9","author":"Maw","year":"2000","journal-title":"Hum. Mol. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib7","first-page":"2908","article-title":"Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice","volume":"118","author":"Yang","year":"2008","journal-title":"J. Clin. Investig"},{"key":"10.1074\/jbc.RA119.008618_bib8","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1186\/s13023-015-0300-3","article-title":"Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation","volume":"10","author":"Boulanger-Scemama","year":"2015","journal-title":"Orphanet J. Rare Dis"},{"key":"10.1074\/jbc.RA119.008618_bib9","doi-asserted-by":"crossref","first-page":"459","DOI":"10.1038\/ejhg.2015.144","article-title":"Homozygosity mapping and whole-genome sequencing reveals a deep intronic PROM1 mutation causing cone-rod dystrophy by pseudoexon activation","volume":"24","author":"Mayer","year":"2016","journal-title":"Eur. J. Hum. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib10","doi-asserted-by":"crossref","first-page":"e95528","DOI":"10.1371\/journal.pone.0095528","article-title":"Molecular diagnosis of putative Stargardt disease by capture next generation sequencing","volume":"9","author":"Zhang","year":"2014","journal-title":"PLoS One"},{"key":"10.1074\/jbc.RA119.008618_bib11","doi-asserted-by":"crossref","first-page":"349","DOI":"10.3109\/13816810.2014.886266","article-title":"Pediatric cone-rod dystrophy with high myopia and nystagmus suggests recessive PROM1 mutations","volume":"36","author":"Khan","year":"2015","journal-title":"Ophthalmic Genet"},{"key":"10.1074\/jbc.RA119.008618_bib12","first-page":"1709","article-title":"Cone-rod dystrophy and a frameshift mutation in the PROM1 gene","volume":"15","author":"Pras","year":"2009","journal-title":"Mol. Vis"},{"key":"10.1074\/jbc.RA119.008618_bib13","doi-asserted-by":"crossref","first-page":"1149","DOI":"10.1167\/iovs.13-13625","article-title":"Identification of mutations causing inherited retinal degenerations in the Israeli and Palestinian populations using homozygosity mapping","volume":"55","author":"Beryozkin","year":"2014","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib14","doi-asserted-by":"crossref","first-page":"5943","DOI":"10.1167\/iovs.10-5797","article-title":"Homozygosity mapping in patients with cone-rod dystrophy: novel mutations and clinical characterizations","volume":"51","author":"Littink","year":"2010","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib15","first-page":"1295","article-title":"An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy","volume":"21","author":"Eidinger","year":"2015","journal-title":"Mol. Vis"},{"key":"10.1074\/jbc.RA119.008618_bib16","doi-asserted-by":"crossref","first-page":"2259","DOI":"10.1167\/iovs.13-13567","article-title":"Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes","volume":"55","author":"Jinda","year":"2014","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib17","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1007\/s00439-014-1512-7","article-title":"Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland","volume":"134","author":"Zhao","year":"2015","journal-title":"Hum. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib18","doi-asserted-by":"crossref","first-page":"e78496","DOI":"10.1371\/journal.pone.0078496","article-title":"Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies","volume":"8","author":"Eisenberger","year":"2013","journal-title":"PLoS One"},{"key":"10.1074\/jbc.RA119.008618_bib19","doi-asserted-by":"crossref","first-page":"2656","DOI":"10.1167\/iovs.09-4857","article-title":"Autosomal recessive retinitis pigmentosa with early macular affectation caused by premature truncation in PROM1","volume":"51","author":"Permanyer","year":"2010","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib20","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1007\/s00439-007-0395-2","article-title":"Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene","volume":"122","author":"Zhang","year":"2007","journal-title":"Hum. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib21","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1167\/iovs.11-8635","article-title":"Prominin-1 localizes to the open rims of outer segment lamellae in Xenopus laevis rod and cone photoreceptors","volume":"53","author":"Han","year":"2012","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib22","doi-asserted-by":"crossref","first-page":"1849","DOI":"10.1002\/dvdy.22307","article-title":"Expression of the zebrafish CD133\/prominin1 genes in cellular proliferation zones in the embryonic central nervous system and sensory organs","volume":"239","author":"McGrail","year":"2010","journal-title":"Dev. Dyn"},{"key":"10.1074\/jbc.RA119.008618_bib23","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1016\/j.preteyeres.2015.12.002","article-title":"PRPH2\/RDS and ROM-1: historical context, current views and future considerations","volume":"52","author":"Stuck","year":"2016","journal-title":"Prog. Retin. Eye Res"},{"key":"10.1074\/jbc.RA119.008618_bib24","doi-asserted-by":"crossref","first-page":"3507","DOI":"10.1093\/hmg\/ddy240","article-title":"Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation","volume":"27","author":"Zulliger","year":"2018","journal-title":"Hum. Mol. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib25","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1080\/13816810.2016.1275022","article-title":"PROM1 gene variations in Brazilian patients with macular dystrophy","volume":"38","author":"Salles","year":"2017","journal-title":"Ophthalmic Genet"},{"key":"10.1074\/jbc.RA119.008618_bib26","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1242\/dmm.017913","article-title":"Biology and therapy of inherited retinal degenerative disease: insights from mouse models","volume":"8","author":"Veleri","year":"2015","journal-title":"Dis. Model. Mech"},{"key":"10.1074\/jbc.RA119.008618_bib27","doi-asserted-by":"crossref","first-page":"bio036632","DOI":"10.1242\/bio.036632","article-title":"Characterisation of maturation of photoreceptor cell subtypes during zebrafish retinal development","volume":"7","author":"Crespo","year":"2018","journal-title":"Biol. Open"},{"key":"10.1074\/jbc.RA119.008618_bib28","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1002\/cne.902600311","article-title":"Early development of photoreceptors in the ventral retina of the zebrafish embryo","volume":"260","author":"Kljavin","year":"1987","journal-title":"J. Comp. Neurol"},{"key":"10.1074\/jbc.RA119.008618_bib29","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1002\/cne.903590403","article-title":"Developmental patterning of rod and cone photoreceptors in embryonic zebrafish","volume":"359","author":"Raymond","year":"1995","journal-title":"J. Comp. Neurol"},{"key":"10.1074\/jbc.RA119.008618_bib30","doi-asserted-by":"crossref","first-page":"515","DOI":"10.1002\/(SICI)1096-9861(19990222)404:4<515::AID-CNE8>3.0.CO;2-A","article-title":"Early retinal development in the zebrafish, Danio rerio: light and electron microscopic analyses","volume":"404","author":"Schmitt","year":"1999","journal-title":"J. Comp. Neurol"},{"key":"10.1074\/jbc.RA119.008618_bib31","doi-asserted-by":"crossref","first-page":"9217","DOI":"10.1074\/jbc.M407166200","article-title":"A novel tetraspanin fusion protein, peripherin-2, requires a region upstream of the fusion domain for activity","volume":"280","author":"Damek-Poprawa","year":"2005","journal-title":"J. Biol. Chem"},{"key":"10.1074\/jbc.RA119.008618_bib32","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1016\/0304-3940(81)90051-3","article-title":"Absence of receptor outer segments in the retina of rds mutant mice","volume":"21","author":"Sanyal","year":"1981","journal-title":"Neurosci. Lett"},{"key":"10.1074\/jbc.RA119.008618_bib33","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1002\/cne.902240107","article-title":"Development and degeneration of retina in rds mutant mice: electron microscopy","volume":"224","author":"Jansen","year":"1984","journal-title":"J. Comp. Neurol"},{"key":"10.1074\/jbc.RA119.008618_bib34","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1016\/j.preteyeres.2008.01.002","article-title":"The spectrum of retinal dystrophies caused by mutations in the peripherin\/RDS gene","volume":"27","author":"Boon","year":"2008","journal-title":"Prog. Retin. Eye Res"},{"key":"10.1074\/jbc.RA119.008618_bib35","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1093\/hmg\/ddn406","article-title":"Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus cones","volume":"18","author":"Chakraborty","year":"2009","journal-title":"Hum. Mol. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib36","doi-asserted-by":"crossref","first-page":"4799","DOI":"10.1093\/hmg\/ddq410","article-title":"Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS","volume":"19","author":"Chakraborty","year":"2010","journal-title":"Hum. Mol. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib37","doi-asserted-by":"crossref","first-page":"27901","DOI":"10.1074\/jbc.M115.683698","article-title":"Retinal degeneration slow (RDS) glycosylation plays a role in cone function and in the regulation of RDS\u00b7ROM-1 protein complex formation","volume":"290","author":"Stuck","year":"2015","journal-title":"J. Biol. Chem"},{"key":"10.1074\/jbc.RA119.008618_bib38","doi-asserted-by":"crossref","first-page":"1144","DOI":"10.1021\/bi701807c","article-title":"Outer segment oligomerization of Rds: evidence from mouse models and subcellular fractionation","volume":"47","author":"Chakraborty","year":"2008","journal-title":"Biochemistry"},{"key":"10.1074\/jbc.RA119.008618_bib39","doi-asserted-by":"crossref","first-page":"5825","DOI":"10.1242\/jcs.01512","article-title":"Myosin 3A transgene expression produces abnormal actin filament bundles in transgenic Xenopus laevis rod photoreceptors","volume":"117","author":"Lin-Jones","year":"2004","journal-title":"J. Cell Sci"},{"key":"10.1074\/jbc.RA119.008618_bib40","first-page":"689","article-title":"The teleost cone cytoskeleton. Localization of actin, microtubules, and intermediate filaments","volume":"27","author":"Nagle","year":"1986","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib41","doi-asserted-by":"crossref","first-page":"381","DOI":"10.1083\/jcb.201202012","article-title":"Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice","volume":"199","author":"Sahly","year":"2012","journal-title":"J. Cell Biol"},{"key":"10.1074\/jbc.RA119.008618_bib42","doi-asserted-by":"crossref","first-page":"585","DOI":"10.1016\/j.exer.2006.03.022","article-title":"Focus on molecules: prominin-1 (CD133)","volume":"85","author":"J\u00e1szai","year":"2007","journal-title":"Exp. Eye Res"},{"key":"10.1074\/jbc.RA119.008618_bib43","doi-asserted-by":"crossref","first-page":"3468","DOI":"10.1096\/fj.14-251397","article-title":"Rim formation is not a prerequisite for distribution of cone photoreceptor outer segment proteins","volume":"28","author":"Conley","year":"2014","journal-title":"FASEB J"},{"key":"10.1074\/jbc.RA119.008618_bib44","doi-asserted-by":"crossref","first-page":"2366","DOI":"10.1167\/iovs.16-21162","article-title":"Prominin-1 is a novel regulator of autophagy in the human retinal pigment epithelium","volume":"58","author":"Bhattacharya","year":"2017","journal-title":"Invest. Ophthalmol. Vis. Sci"},{"key":"10.1074\/jbc.RA119.008618_bib45","doi-asserted-by":"crossref","first-page":"1821","DOI":"10.1080\/15548627.2015.1084456","article-title":"Autophagy supports color vision","volume":"11","author":"Zhou","year":"2015","journal-title":"Autophagy"},{"key":"10.1074\/jbc.RA119.008618_bib46","doi-asserted-by":"crossref","first-page":"562","DOI":"10.1096\/fj.03-0289fje","article-title":"Inhibition of the ATP-driven proton pump in RPE lysosomes by the major lipofuscin fluorophore A2-E may contribute to the pathogenesis of age-related macular degeneration","volume":"18","author":"Bergmann","year":"2004","journal-title":"FASEB J"},{"key":"10.1074\/jbc.RA119.008618_bib47","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1080\/15548627.2018.1520548","article-title":"CERKL regulates autophagy via the NAD-dependent deacetylase SIRT1","volume":"15","author":"Hu","year":"2019","journal-title":"Autophagy"},{"key":"10.1074\/jbc.RA119.008618_bib48","doi-asserted-by":"crossref","first-page":"2335","DOI":"10.1093\/hmg\/ddx137","article-title":"CERKL gene knockout disturbs photoreceptor outer segment phagocytosis and causes rod-cone dystrophy in zebrafish","volume":"26","author":"Yu","year":"2017","journal-title":"Hum. Mol. Genet"},{"key":"10.1074\/jbc.RA119.008618_bib49","doi-asserted-by":"crossref","first-page":"6225","DOI":"10.1074\/jbc.M116.760314","article-title":"Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafish","volume":"292","author":"Liu","year":"2017","journal-title":"J. Biol. Chem"},{"key":"10.1074\/jbc.RA119.008618_bib50","doi-asserted-by":"crossref","first-page":"46098","DOI":"10.1038\/srep46098","article-title":"Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy","volume":"7","author":"Lu","year":"2017","journal-title":"Sci. Rep"}],"container-title":["Journal of Biological Chemistry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0021925820320810?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0021925820320810?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1074\/jbc.RA119.008618","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,12,16]],"date-time":"2021-12-16T19:53:16Z","timestamp":1639684396000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0021925820320810"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,9]]},"references-count":50,"journal-issue":{"issue":"38","published-print":{"date-parts":[[2019,9]]}},"alternative-id":["S0021925820320810"],"URL":"https:\/\/doi.org\/10.1074\/jbc.ra119.008618","relation":{},"ISSN":["0021-9258"],"issn-type":[{"value":"0021-9258","type":"print"}],"subject":[],"published":{"date-parts":[[2019,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration","name":"articletitle","label":"Article Title"},{"value":"Journal of Biological Chemistry","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1074\/jbc.RA119.008618","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Lu et al.","name":"copyright","label":"Copyright"}]}}