Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients

Autores
Cuadrado Vilanova, Maria; Burgueño, Victor; Balaguer Lluna, Leire; Aschero, Rosario; Castillo Ecija, Helena; Liu, Jing; Perez Jaume, Sara; Pascual Pasto, Guillem; Olaciregui, Nagore G; Gomez Gonzalez, Soledad; Correa, Genoveva; Suñol, Mariona; Schaiquevich, Paula Susana; Radvanyi, François; Lavarino, Cinzia; Mora, Jaume; Catala Mora, Jaume; Chantada, Guillermo Luis; Carcaboso, Angel M.
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fundoscopy is the standard method for diagnosis and follow-up of intraocular retinoblastoma, but it is sometimes insufficient to discern whether tumors are inactivated following treatments. In this work, we hypothesized that the amount of conserved nuclear DNA sequences in the cell-free DNA (cfDNA) fraction of the aqueous humor (AH) might complement fundoscopy for retinoblastoma follow-up. To address our hypothesis, we developed highly sensitive droplet digital polymerase chain reaction (ddPCR) methods to quantify highly conserved DNA sequences of nucleus-encoded genes (GAPDH and B4GALNT1) and of a mitochondrial gene, MT-ATP6. We obtained AH samples during intravitreal treatments. We analyzed 42 AH samples from 25 patients with intraocular retinoblastoma and 11 AH from controls (non-cancer patients). According to clinical criteria, we grouped patients as having progression-free or progressive retinoblastoma. cfDNA concentration in the AH was similar in both retinoblastoma groups. Copy counts for nucleus-derived sequences of GAPDH and B4GALNT1 were significantly higher in the AH from patients with progressive disease, compared to the AH from progression-free patients and control non-cancer patients. The presence of mitochondrial DNA in the AH explained that both retinoblastoma groups had similar cfDNA concentration in AH. The optimal cut-off point for discriminating between progressive and progression-free retinoblastomas was 108 GAPDH copies per reaction. Among patients having serial AH samples analyzed during their intravitreal chemotherapy, GAPDH copies were high and decreased below the cut-off point in those patients responding to chemotherapy. In contrast, one non-responder patient remained with values above the cut-off during follow-up, until enucleation. We conclude that the measurement of conserved nuclear gene sequences in AH allows follow-up of intraocular retinoblastoma during intravitreal treatment. The method is applicable to all patients and could be relevant for those in which fundoscopy evaluation is inconclusive.
Fil: Cuadrado Vilanova, Maria. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; España
Fil: Burgueño, Victor. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Balaguer Lluna, Leire. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Aschero, Rosario. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Castillo Ecija, Helena. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; España
Fil: Liu, Jing. Centre National de la Recherche Scientifique; Francia. Institute Curie; Francia
Fil: Perez Jaume, Sara. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Pascual Pasto, Guillem. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Olaciregui, Nagore G. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Gomez Gonzalez, Soledad. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; España
Fil: Correa, Genoveva. Hospital Hm Nens; España
Fil: Suñol, Mariona. Hospital Sant Joan de Deu Barcelona; España
Fil: Schaiquevich, Paula Susana. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina
Fil: Radvanyi, François. Centre National de la Recherche Scientifique; Francia. Institute Curie; Francia
Fil: Lavarino, Cinzia. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Mora, Jaume. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Catala Mora, Jaume. Hospital Sant Joan de Deu Barcelona; España
Fil: Chantada, Guillermo Luis. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Carcaboso, Angel M.. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Materia
AQUEOUS HUMOR
BIOMARKERS
DROPLET DIGITAL POLYMERASE CHAIN REACTION
EYE
INTRAVITREAL CHEMOTHERAPY
LIQUID BIOPSY
MITOCHONDRIAL DNA
NEOPLASIA
NUCLEAR DNA
RETINOBLASTOMA
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/229200

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patientsCuadrado Vilanova, MariaBurgueño, VictorBalaguer Lluna, LeireAschero, RosarioCastillo Ecija, HelenaLiu, JingPerez Jaume, SaraPascual Pasto, GuillemOlaciregui, Nagore GGomez Gonzalez, SoledadCorrea, GenovevaSuñol, MarionaSchaiquevich, Paula SusanaRadvanyi, FrançoisLavarino, CinziaMora, JaumeCatala Mora, JaumeChantada, Guillermo LuisCarcaboso, Angel M.AQUEOUS HUMORBIOMARKERSDROPLET DIGITAL POLYMERASE CHAIN REACTIONEYEINTRAVITREAL CHEMOTHERAPYLIQUID BIOPSYMITOCHONDRIAL DNANEOPLASIANUCLEAR DNARETINOBLASTOMAhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Fundoscopy is the standard method for diagnosis and follow-up of intraocular retinoblastoma, but it is sometimes insufficient to discern whether tumors are inactivated following treatments. In this work, we hypothesized that the amount of conserved nuclear DNA sequences in the cell-free DNA (cfDNA) fraction of the aqueous humor (AH) might complement fundoscopy for retinoblastoma follow-up. To address our hypothesis, we developed highly sensitive droplet digital polymerase chain reaction (ddPCR) methods to quantify highly conserved DNA sequences of nucleus-encoded genes (GAPDH and B4GALNT1) and of a mitochondrial gene, MT-ATP6. We obtained AH samples during intravitreal treatments. We analyzed 42 AH samples from 25 patients with intraocular retinoblastoma and 11 AH from controls (non-cancer patients). According to clinical criteria, we grouped patients as having progression-free or progressive retinoblastoma. cfDNA concentration in the AH was similar in both retinoblastoma groups. Copy counts for nucleus-derived sequences of GAPDH and B4GALNT1 were significantly higher in the AH from patients with progressive disease, compared to the AH from progression-free patients and control non-cancer patients. The presence of mitochondrial DNA in the AH explained that both retinoblastoma groups had similar cfDNA concentration in AH. The optimal cut-off point for discriminating between progressive and progression-free retinoblastomas was 108 GAPDH copies per reaction. Among patients having serial AH samples analyzed during their intravitreal chemotherapy, GAPDH copies were high and decreased below the cut-off point in those patients responding to chemotherapy. In contrast, one non-responder patient remained with values above the cut-off during follow-up, until enucleation. We conclude that the measurement of conserved nuclear gene sequences in AH allows follow-up of intraocular retinoblastoma during intravitreal treatment. The method is applicable to all patients and could be relevant for those in which fundoscopy evaluation is inconclusive.Fil: Cuadrado Vilanova, Maria. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; EspañaFil: Burgueño, Victor. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Balaguer Lluna, Leire. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Aschero, Rosario. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Castillo Ecija, Helena. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; EspañaFil: Liu, Jing. Centre National de la Recherche Scientifique; Francia. Institute Curie; FranciaFil: Perez Jaume, Sara. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Pascual Pasto, Guillem. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Olaciregui, Nagore G. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Gomez Gonzalez, Soledad. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; EspañaFil: Correa, Genoveva. Hospital Hm Nens; EspañaFil: Suñol, Mariona. Hospital Sant Joan de Deu Barcelona; EspañaFil: Schaiquevich, Paula Susana. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; ArgentinaFil: Radvanyi, François. Centre National de la Recherche Scientifique; Francia. Institute Curie; FranciaFil: Lavarino, Cinzia. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Mora, Jaume. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Catala Mora, Jaume. Hospital Sant Joan de Deu Barcelona; EspañaFil: Chantada, Guillermo Luis. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaFil: Carcaboso, Angel M.. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; EspañaJohn Wiley & Sons2023-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/229200Cuadrado Vilanova, Maria; Burgueño, Victor; Balaguer Lluna, Leire; Aschero, Rosario; Castillo Ecija, Helena; et al.; Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients; John Wiley & Sons; Journal of Pathology: Clinical Research; 9; 1; 1-2023; 32-432056-4538CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/cjp2.296info:eu-repo/semantics/altIdentifier/url/https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/cjp2.296info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:46:17Zoai:ri.conicet.gov.ar:11336/229200instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:46:17.591CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
title Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
spellingShingle Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
Cuadrado Vilanova, Maria
AQUEOUS HUMOR
BIOMARKERS
DROPLET DIGITAL POLYMERASE CHAIN REACTION
EYE
INTRAVITREAL CHEMOTHERAPY
LIQUID BIOPSY
MITOCHONDRIAL DNA
NEOPLASIA
NUCLEAR DNA
RETINOBLASTOMA
title_short Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
title_full Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
title_fullStr Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
title_full_unstemmed Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
title_sort Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients
dc.creator.none.fl_str_mv Cuadrado Vilanova, Maria
Burgueño, Victor
Balaguer Lluna, Leire
Aschero, Rosario
Castillo Ecija, Helena
Liu, Jing
Perez Jaume, Sara
Pascual Pasto, Guillem
Olaciregui, Nagore G
Gomez Gonzalez, Soledad
Correa, Genoveva
Suñol, Mariona
Schaiquevich, Paula Susana
Radvanyi, François
Lavarino, Cinzia
Mora, Jaume
Catala Mora, Jaume
Chantada, Guillermo Luis
Carcaboso, Angel M.
author Cuadrado Vilanova, Maria
author_facet Cuadrado Vilanova, Maria
Burgueño, Victor
Balaguer Lluna, Leire
Aschero, Rosario
Castillo Ecija, Helena
Liu, Jing
Perez Jaume, Sara
Pascual Pasto, Guillem
Olaciregui, Nagore G
Gomez Gonzalez, Soledad
Correa, Genoveva
Suñol, Mariona
Schaiquevich, Paula Susana
Radvanyi, François
Lavarino, Cinzia
Mora, Jaume
Catala Mora, Jaume
Chantada, Guillermo Luis
Carcaboso, Angel M.
author_role author
author2 Burgueño, Victor
Balaguer Lluna, Leire
Aschero, Rosario
Castillo Ecija, Helena
Liu, Jing
Perez Jaume, Sara
Pascual Pasto, Guillem
Olaciregui, Nagore G
Gomez Gonzalez, Soledad
Correa, Genoveva
Suñol, Mariona
Schaiquevich, Paula Susana
Radvanyi, François
Lavarino, Cinzia
Mora, Jaume
Catala Mora, Jaume
Chantada, Guillermo Luis
Carcaboso, Angel M.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv AQUEOUS HUMOR
BIOMARKERS
DROPLET DIGITAL POLYMERASE CHAIN REACTION
EYE
INTRAVITREAL CHEMOTHERAPY
LIQUID BIOPSY
MITOCHONDRIAL DNA
NEOPLASIA
NUCLEAR DNA
RETINOBLASTOMA
topic AQUEOUS HUMOR
BIOMARKERS
DROPLET DIGITAL POLYMERASE CHAIN REACTION
EYE
INTRAVITREAL CHEMOTHERAPY
LIQUID BIOPSY
MITOCHONDRIAL DNA
NEOPLASIA
NUCLEAR DNA
RETINOBLASTOMA
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.2
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Fundoscopy is the standard method for diagnosis and follow-up of intraocular retinoblastoma, but it is sometimes insufficient to discern whether tumors are inactivated following treatments. In this work, we hypothesized that the amount of conserved nuclear DNA sequences in the cell-free DNA (cfDNA) fraction of the aqueous humor (AH) might complement fundoscopy for retinoblastoma follow-up. To address our hypothesis, we developed highly sensitive droplet digital polymerase chain reaction (ddPCR) methods to quantify highly conserved DNA sequences of nucleus-encoded genes (GAPDH and B4GALNT1) and of a mitochondrial gene, MT-ATP6. We obtained AH samples during intravitreal treatments. We analyzed 42 AH samples from 25 patients with intraocular retinoblastoma and 11 AH from controls (non-cancer patients). According to clinical criteria, we grouped patients as having progression-free or progressive retinoblastoma. cfDNA concentration in the AH was similar in both retinoblastoma groups. Copy counts for nucleus-derived sequences of GAPDH and B4GALNT1 were significantly higher in the AH from patients with progressive disease, compared to the AH from progression-free patients and control non-cancer patients. The presence of mitochondrial DNA in the AH explained that both retinoblastoma groups had similar cfDNA concentration in AH. The optimal cut-off point for discriminating between progressive and progression-free retinoblastomas was 108 GAPDH copies per reaction. Among patients having serial AH samples analyzed during their intravitreal chemotherapy, GAPDH copies were high and decreased below the cut-off point in those patients responding to chemotherapy. In contrast, one non-responder patient remained with values above the cut-off during follow-up, until enucleation. We conclude that the measurement of conserved nuclear gene sequences in AH allows follow-up of intraocular retinoblastoma during intravitreal treatment. The method is applicable to all patients and could be relevant for those in which fundoscopy evaluation is inconclusive.
Fil: Cuadrado Vilanova, Maria. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; España
Fil: Burgueño, Victor. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Balaguer Lluna, Leire. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Aschero, Rosario. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Castillo Ecija, Helena. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; España
Fil: Liu, Jing. Centre National de la Recherche Scientifique; Francia. Institute Curie; Francia
Fil: Perez Jaume, Sara. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Pascual Pasto, Guillem. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Olaciregui, Nagore G. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Gomez Gonzalez, Soledad. Institut de Recerca Sant Joan de Déu; España. Hospital Sant Joan de Deu Barcelona; España
Fil: Correa, Genoveva. Hospital Hm Nens; España
Fil: Suñol, Mariona. Hospital Sant Joan de Deu Barcelona; España
Fil: Schaiquevich, Paula Susana. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina
Fil: Radvanyi, François. Centre National de la Recherche Scientifique; Francia. Institute Curie; Francia
Fil: Lavarino, Cinzia. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Mora, Jaume. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Catala Mora, Jaume. Hospital Sant Joan de Deu Barcelona; España
Fil: Chantada, Guillermo Luis. Universidad Austral. Facultad de Ciencias Biomédicas. Instituto de Investigaciones en Medicina Traslacional. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones en Medicina Traslacional; Argentina. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
Fil: Carcaboso, Angel M.. Hospital Sant Joan de Deu Barcelona; España. Institut de Recerca Sant Joan de Déu; España
description Fundoscopy is the standard method for diagnosis and follow-up of intraocular retinoblastoma, but it is sometimes insufficient to discern whether tumors are inactivated following treatments. In this work, we hypothesized that the amount of conserved nuclear DNA sequences in the cell-free DNA (cfDNA) fraction of the aqueous humor (AH) might complement fundoscopy for retinoblastoma follow-up. To address our hypothesis, we developed highly sensitive droplet digital polymerase chain reaction (ddPCR) methods to quantify highly conserved DNA sequences of nucleus-encoded genes (GAPDH and B4GALNT1) and of a mitochondrial gene, MT-ATP6. We obtained AH samples during intravitreal treatments. We analyzed 42 AH samples from 25 patients with intraocular retinoblastoma and 11 AH from controls (non-cancer patients). According to clinical criteria, we grouped patients as having progression-free or progressive retinoblastoma. cfDNA concentration in the AH was similar in both retinoblastoma groups. Copy counts for nucleus-derived sequences of GAPDH and B4GALNT1 were significantly higher in the AH from patients with progressive disease, compared to the AH from progression-free patients and control non-cancer patients. The presence of mitochondrial DNA in the AH explained that both retinoblastoma groups had similar cfDNA concentration in AH. The optimal cut-off point for discriminating between progressive and progression-free retinoblastomas was 108 GAPDH copies per reaction. Among patients having serial AH samples analyzed during their intravitreal chemotherapy, GAPDH copies were high and decreased below the cut-off point in those patients responding to chemotherapy. In contrast, one non-responder patient remained with values above the cut-off during follow-up, until enucleation. We conclude that the measurement of conserved nuclear gene sequences in AH allows follow-up of intraocular retinoblastoma during intravitreal treatment. The method is applicable to all patients and could be relevant for those in which fundoscopy evaluation is inconclusive.
publishDate 2023
dc.date.none.fl_str_mv 2023-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/229200
Cuadrado Vilanova, Maria; Burgueño, Victor; Balaguer Lluna, Leire; Aschero, Rosario; Castillo Ecija, Helena; et al.; Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients; John Wiley & Sons; Journal of Pathology: Clinical Research; 9; 1; 1-2023; 32-43
2056-4538
CONICET Digital
CONICET
url http://hdl.handle.net/11336/229200
identifier_str_mv Cuadrado Vilanova, Maria; Burgueño, Victor; Balaguer Lluna, Leire; Aschero, Rosario; Castillo Ecija, Helena; et al.; Follow-up of intraocular retinoblastoma through the quantitative analysis of conserved nuclear DNA sequences in aqueous humor from patients; John Wiley & Sons; Journal of Pathology: Clinical Research; 9; 1; 1-2023; 32-43
2056-4538
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1002/cjp2.296
info:eu-repo/semantics/altIdentifier/url/https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/cjp2.296
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
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application/pdf
dc.publisher.none.fl_str_mv John Wiley & Sons
publisher.none.fl_str_mv John Wiley & Sons
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