Escribano Julio相关文献与解析，生知库 | 链接生命科学的每一步

Moreno-Fernández, Alberto; Domínguez-Jurado, Elena; Martínez de Sarasa Buchaca, Marc; Blas, Sofía; Noblejas-López, María Del Mar; Moya, Carmen; de Andrés, Fernando; Bravo, Iván; Aroca-Aguilar, Jose-Daniel; Ferre-Fernández, Jesús-José; Escribano, Julio; Rodríguez-Diéguez, Antonio; Salcedo-Abraira, Pablo; García-Yuste, Santiago; Alonso-Moreno, Carlos; Lara-Sánchez, Agustín

肿瘤

乳腺癌

肿瘤免疫

发表日期：2026

文献求助收藏

The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease.

儿童青光眼中四种基质金属蛋白酶相关基因罕见变异负担的增加表明该疾病的遗传方式复杂

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms25115757

Tevar Angel, Aroca-Aguilar JosÃ©-Daniel, Bonet-FernÃ¡ndez Juan-Manuel, Atienzar-Aroca Raquel, Campos-Mollo Ezequiel, MÃ©ndez-HernÃ¡ndez Carmen, Morales-FernÃ¡ndez Laura, Leal Palmer IÃ±aki, Coca-Prados Miguel, Martinez-de-la-Casa Jose-Maria, Garcia-Feijoo Julian, Escribano Julio

其它

发表日期：2024

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Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma

原发性先天性青光眼中房角发育不良的变异性和CYP1B1基因型的活性

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0176386

García-Antón, María T; Salazar, Juan J; de Hoz, Rosa; Rojas, Blanca; Ramírez, Ana I; Triviño, Alberto; Aroca-Aguilar, José-Daniel; García-Feijoo, Julián; Escribano, Julio; Ramírez, José M

Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences

先天性青光眼中罕见的FOXC1变异：翻译调控序列的鉴定

期刊:European Journal of Human Genetics

影响因子:4.6

doi:10.1038/ejhg.2015.169

Medina-Trillo, Cristina; Aroca-Aguilar, José-Daniel; Méndez-Hernández, Carmen-Dora; Morales, Laura; García-Antón, Maite; García-Feijoo, Julián; Escribano, Julio

Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability.

显性青光眼中的低效和高效 FOXC1 突变：转录激活和表型变异

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0119272

Medina-Trillo Cristina, SÃ¡nchez-SÃ¡nchez Francisco, Aroca-Aguilar JosÃ©-Daniel, Ferre-FernÃ¡ndez JesÃºs-JosÃ©, Morales Laura, MÃ©ndez-HernÃ¡ndez Carmen-Dora, Blanco-Kelly Fiona, Ayuso Carmen, GarcÃa-Feijoo JuliÃ¡n, Escribano Julio

LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients

LOXL1基因变异及其与西班牙患者假性剥脱性青光眼（XFG）的关联

期刊:BMC Medical Genetics

影响因子:

doi:10.1186/s12881-015-0221-y

Álvarez, Lydia; García, Montserrat; González-Iglesias, Héctor; Escribano, Julio; Rodríguez-Calvo, Pedro P; Fernández-Vega, Luis; Coca-Prados, Miguel

Functional role of proteolytic processing of recombinant myocilin in self-aggregation

重组肌纤蛋白的蛋白水解加工在自身聚集中的功能作用

期刊:Investigative Ophthalmology & Visual Science

影响因子:4.7

doi:10.1167/iovs.09-4118

Aroca-Aguilar, José-Daniel; Martínez-Redondo, Francisco; Sánchez-Sánchez, Francisco; Coca-Prados, Miguel; Escribano, Julio

发表日期：2010

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Exploring Gallium(III) Complexes as Emerging Therapeutic Candidates for Breast Cancer

探索镓(III)配合物作为乳腺癌新兴治疗候选药物

The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease.

儿童青光眼中四种基质金属蛋白酶相关基因罕见变异负担的增加表明该疾病的遗传方式复杂

Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma

原发性先天性青光眼中房角发育不良的变异性和CYP1B1基因型的活性

Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences

先天性青光眼中罕见的FOXC1变异：翻译调控序列的鉴定

Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability.

显性青光眼中的低效和高效 FOXC1 突变：转录激活和表型变异

LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients

LOXL1基因变异及其与西班牙患者假性剥脱性青光眼（XFG）的关联

Functional role of proteolytic processing of recombinant myocilin in self-aggregation

重组肌纤蛋白的蛋白水解加工在自身聚集中的功能作用