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1Academic Journal
المؤلفون: Zeitz, Christina, Navarro, Julien, Azizzadeh Pormehr, Leila, Méjécase, Cécile, M. Neves, Luiza, Letellier, Camille, Condroyer, Christel, Albadri, Shahad, Amprou, Andréa, Antonio, Aline, Ben-Yacoub, Tasnim, Wohlschlegel, Juliette, Andrieu, Camille, Serafini, Malo, Bianco, Lorenzo, Antropoli, Alessio, Nassisi, Marco, El Shamieh, Said, Chantot-Bastaraud, Sandra, Mohand-Saïd, Saddek, Smirnov, Vasily, Sahel, José-Alain, del Bene, Filippo, Audo, Isabelle
المساهمون: Institut de la Vision, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie bactérienne (LCB), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Beirut Arab University Beyrouth, Liban (BAU), CHU Trousseau APHP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Service de pathologie CHU Lille, Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille)
المصدر: ISSN: 1098-3600.
مصطلحات موضوعية: UBAP1L, autosomal recessive rod-cone and cone-rod dystrophy, novel gene defect, genome sequencing, retinal organoids, retinal pigment epithelium, zebrafish, 3D-modelling, [SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, [SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE]
Relation: info:eu-repo/semantics/altIdentifier/pmid/38293907; PUBMED: 38293907
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2Academic Journal
المؤلفون: Zeitz, Christina, Navarro, Julien, Azizzadeh Pormehr, Leila, Méjécase, Cécile, Neves, Luiza M., Letellier, Camille, Condroyer, Christel, Albadri, Shahad, Amprou, Andréa, Antonio, Aline, Ben-Yacoub, Tasnim, Wohlschlegel, Juliette, Andrieu, Camille, Serafini, Malo, Bianco, Lorenzo, Antropoli, Alessio, Nassisi, Marco, El Shamieh, Said, Chantot-Bastaraud, Sandra, Mohand-Saïd, Saddek, Smirnov, Vasily, Sahel, José-Alain, Del Bene, Filippo, Audo, Isabelle
المساهمون: C. Zeitz, J. Navarro, L. Azizzadeh Pormehr, C. Méjécase, L.M. Neve, C. Letellier, C. Condroyer, S. Albadri, A. Amprou, A. Antonio, T. Ben-Yacoub, J. Wohlschlegel, C. Andrieu, M. Serafini, L. Bianco, A. Antropoli, M. Nassisi, S. El Shamieh, S. Chantot-Bastaraud, S. Mohand-Saïd, V. Smirnov, J. Sahel, F. Del Bene, I. Audo
مصطلحات موضوعية: Autosomal recessive rod-cone and cone-rod dystrophy, Genome sequencing, Novel gene defect, Retinal organoid, Zebrafish, Settore MED/30 - Malattie Apparato Visivo, Settore BIO/18 - Genetica
Relation: info:eu-repo/semantics/altIdentifier/pmid/38293907; info:eu-repo/semantics/altIdentifier/wos/WOS:001250875600001; volume:26; issue:6; firstpage:1; lastpage:12; numberofpages:12; journal:GENETICS IN MEDICINE; https://hdl.handle.net/2434/1057012; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85187359688