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Departamento de Ciencia y Tecnología Agroforestal y Genética

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Scopus Author ID: 8578460900

Biography

Personal Docente e Investigador de la Universidad de Castilla-La Mancha, adscrito al Departamento de Ciencia y Tecnología Agroforestal y Genética

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Employment (1)

Universidad de Castilla-La Mancha: Campus de Albacete, Castilla-La Mancha, ES

Profesor Titular de Universidad (Departamento de Ciencia y Tecnología Agroforestal y Genética)
Employment
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Universidad de Castilla-La Mancha

Works (49)

Brief Report: Evidence of Autism Spectrum Disorder Caused by a Mutation in ATRX Gene: A Case Report

Journal of Autism and Developmental Disorders
2024-01 | Journal article
DOI: 10.1007/s10803-022-05588-x
Contributors: María-Pilar López-Garrido; María-Carmen Carrascosa-Romero; Minerva Montero-Hernández; Jesús Ruiz-Almansa; Francisco Sánchez-Sánchez
Source: check_circle
Crossref

Self-Renewal Inhibition in Breast Cancer Stem Cells: Moonlight Role of PEDF in Breast Cancer.

Cancers
2023-11 | Journal article
DOI: 10.3390/cancers15225422
PMID: 38001682
Contributors: Gil-Gas C; Sánchez-Díez M; Honrubia-Gómez P; Sánchez-Sánchez JL; Alvarez-Simón CB; Sabater S; Sánchez-Sánchez F; Ramírez-Castillejo C
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Moonlight role of PEDF in breast cancer: self-renewal inhibition in breast cancer stem cells

2023-09 | Preprint
DOI: 10.21203/rs.3.rs-2636130/v1
PPR: PPR719877
Contributors: Gil-Gas C; Sánchez-Díez M; Honrubia-Gómez P; Sánchez-Sánchez JL; Alvarez-Simón CB; Sabater S; Sánchez-Sánchez F; Ramirez-Castillejo C
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Case Report: Precision genetic diagnosis in a case of Dyggve-Melchior-Clausen syndrome reveals paternal isodisomy and heterodisomy of chromosome 18 with imprinting clinical implications.

Frontiers in genetics
2022-11 | Journal article
DOI: 10.3389/fgene.2022.1005573
PMID: 36468000
PMC: PMC9716064
Contributors: López-Garrido MP; Carrascosa-Romero MC; Montero-Hernández M; Serrano-Martínez CM; Sánchez-Sánchez F
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Evidence of Autism Spectrum Disorder Caused By A Mutation In ATRX Gene

2021-10-20 | Preprint
DOI: 10.21203/rs.3.rs-965145/v1
Contributors: María-Pilar López-Garrido; María-Carmen Carrascosa-Romero; Minerva Montero-Hernández; Jesús Ruiz-Almansa; Francisco Sánchez-Sánchez
Source: check_circle
Crossref

Pedf derived peptides affect colorectal cancer cell lines resistance and tumour re-growth capacity.

Oncotarget
2019-04 | Journal article
DOI: 10.18632/oncotarget.26085
PMID: 31105879
PMC: PMC6508205
Contributors: Honrubia-Gómez P; López-Garrido MP; Gil-Gas C; Sánchez-Sánchez J; Alvarez-Simon C; Cuenca-Escalona J; Perez AF; Arias E; Moreno R; Sánchez-Sánchez F et al.
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Molecular and neurochemical substrates of the audiogenic seizure strains: The GASH:Sal model.

Epilepsy & behavior : E&B
2015-06 | Journal article
DOI: 10.1016/j.yebeh.2015.05.025
PMID: 26071997
Contributors: Prieto-Martín AI; Aroca-Aguilar JD; Sánchez-Sánchez F; Muñoz LJ; López DE; Escribano J; de Cabo C
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

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

PloS one
2015-03 | Journal article
DOI: 10.1371/journal.pone.0119272
PMID: 25786029
PMC: PMC4364892
Contributors: Medina-Trillo C; Sánchez-Sánchez F; Aroca-Aguilar JD; Ferre-Fernández JJ; Morales L; Méndez-Hernández CD; Blanco-Kelly F; Ayuso C; García-Feijoo J; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Defects in subventricular zone pigmented epithelium-derived factor niche signaling in the senescence-accelerated mouse prone-8.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
2015-01 | Journal article
DOI: 10.1096/fj.13-244442
PMID: 25636741
Contributors: Castro-Garcia P; Díaz-Moreno M; Gil-Gas C; Fernández-Gómez FJ; Honrubia-Gómez P; Álvarez-Simón CB; Sánchez-Sánchez F; Cano JC; Almeida F; Blanco V et al.
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

WDR36 and P53 gene variants and susceptibility to primary open-angle glaucoma: analysis of gene-gene interactions.

Investigative ophthalmology & visual science
2011-10 | Journal article
DOI: 10.1167/iovs.11-7489
PMID: 21931130
PMC: PMC3208188
Contributors: Blanco-Marchite C; Sánchez-Sánchez F; López-Garrido MP; Iñigez-de-Onzoño M; López-Martínez F; López-Sánchez E; Alvarez L; Rodríguez-Calvo PP; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

GSTT1, GSTM1, and CYP1B1 gene polymorphisms and susceptibility to sporadic renal cell cancer.

Urologic oncology
2011-04 | Journal article
DOI: 10.1016/j.urolonc.2010.10.001
PMID: 21458313
Contributors: Salinas-Sánchez AS; Sánchez-Sánchez F; Donate-Moreno MJ; Rubio-del-Campo A; Serrano-Oviedo L; Gimenez-Bachs JM; Martínez-Sanchiz C; Segura-Martín M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Interaction of recombinant myocilin with the matricellular protein SPARC: functional implications.

Investigative ophthalmology & visual science
2011-01 | Journal article
DOI: 10.1167/iovs.09-4866
PMID: 20926826
PMC: PMC3053273
Contributors: Aroca-Aguilar JD; Sánchez-Sánchez F; Ghosh S; Fernández-Navarro A; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Polymorphic deletions of the GSTT1 and GSTM1 genes and susceptibility to bladder cancer.

BJU international
2010-10 | Journal article
DOI: 10.1111/j.1464-410x.2010.09683.x
PMID: 20942828
Contributors: Salinas-Sánchez AS; Sánchez-Sánchez F; Donate-Moreno MJ; Rubio-del-Campo A; Gimenez-Bachs JM; Lorenzo-Romero JG; Serrano-Oviedo L; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Functional analysis of CYP1B1 mutations and association of heterozygous hypomorphic alleles with primary open-angle glaucoma.

Clinical genetics
2009-09 | Journal article
DOI: 10.1111/j.1399-0004.2009.01284.x
PMID: 19793111
Contributors: López-Garrido MP; Blanco-Marchite C; Sánchez-Sánchez F; López-Sánchez E; Chaqués-Alepuz V; Campos-Mollo E; Salinas-Sánchez AS; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

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

Investigative ophthalmology & visual science
2009-08 | Journal article
DOI: 10.1167/iovs.09-4118
PMID: 19696176
PMC: PMC2869055
Contributors: Aroca-Aguilar JD; Martínez-Redondo F; Sánchez-Sánchez F; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

An update on the biology of cancer stem cells in breast cancer.

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
2008-12 | Journal article
DOI: 10.1007/s12094-008-0291-9
PMID: 19068449
Contributors: García Bueno JM; Ocaña A; Castro-García P; Gil Gas C; Sánchez-Sánchez F; Poblet E; Serrano R; Calero R; Ramírez-Castillejo C
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Heterozygous expression of myocilin glaucoma mutants increases secretion of the mutant forms and reduces extracellular processed myocilin.

Molecular vision
2008-11 | Journal article
PMID: 19023451
PMC: PMC2585175
Contributors: Aroca-Aguilar JD; Sánchez-Sánchez F; Martínez-Redondo F; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Nonsense-mediated decay: paving the road for genome diversification.

BioEssays : news and reviews in molecular, cellular and developmental biology
2008-10 | Journal article
DOI: 10.1002/bies.20825
PMID: 18798540
Contributors: Sánchez-Sánchez F; Mittnacht S
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Implications of mismatch repair genes hMLH1 and hMSH2 in patients with sporadic renal cell carcinoma.

BJU international
2008-03 | Journal article
DOI: 10.1111/j.1464-410x.2008.07581.x
PMID: 18325052
Contributors: Rubio-Del-Campo A; Salinas-Sánchez AS; Sánchez-Sánchez F; Giménez-Bachs JM; Donate-Moreno MJ; Pastor-Navarro H; Carrión-López P; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Implications of p53 gene mutations on patient survival in transitional cell carcinoma of the bladder: a long-term study.

Urologic oncology
2008-03 | Journal article
DOI: 10.1016/j.urolonc.2007.07.011
PMID: 18367096
Contributors: Salinas-Sánchez AS; Lorenzo-Romero JG; Giménez-Bachs JM; Sánchez-Sánchez F; Donate-Moreno MJ; Rubio-Del-Campo A; Hernández-Millán IR; Escribano-Martínez J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Expression and purification of functional recombinant human pigment epithelium-derived factor (PEDF) secreted by the yeast Pichia pastoris.

Journal of biotechnology
2008-01 | Journal article
DOI: 10.1016/j.jbiotec.2008.01.005
PMID: 18282627
Contributors: Sánchez-Sánchez F; Aroca-Aguilar JD; Segura I; Ramírez-Castillejo C; Riese HH; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Crystal structure of the retinoblastoma protein N domain provides insight into tumor suppression, ligand interaction, and holoprotein architecture.

Molecular cell
2007-11 | Journal article
DOI: 10.1016/j.molcel.2007.08.023
PMID: 17996702
PMC: PMC4944837
Contributors: Hassler M; Singh S; Yue WW; Luczynski M; Lakbir R; Sanchez-Sanchez F; Bader T; Pearl LH; Mittnacht S
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

VHL protein alterations in sporadic renal cell carcinoma.

Clinical oncology (Royal College of Radiologists (Great Britain))
2007-10 | Journal article
DOI: 10.1016/j.clon.2007.08.014
PMID: 17919893
Contributors: Giménez-Bachs JM; Salinas-Sánchez AS; Sánchez-Sánchez F; Lorenzo-Romero JG; Donate-Moreno MJ; Pastor-Navarro H; Carrión-López P; Virseda-Rodríguez JA
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

MYOC gene mutations in Spanish patients with autosomal dominant primary open-angle glaucoma: a founder effect in southeast Spain.

Molecular vision
2007-09 | Journal article
PMID: 17893668
Contributors: Campos-Mollo E; Sánchez-Sánchez F; López-Garrido MP; López-Sánchez E; López-Martínez F; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

R124C and R555W TGFBI mutations in Spanish families with autosomal-dominant corneal dystrophies.

Molecular vision
2007-08 | Journal article
PMID: 17768377
Contributors: Blanco-Marchite C; Sánchez-Sánchez F; López-Sánchez E; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Characterization of the intracellular proteolytic cleavage of myocilin and identification of calpain II as a myocilin-processing protease.

The Journal of biological chemistry
2007-07 | Journal article
DOI: 10.1074/jbc.m609608200
PMID: 17650508
Contributors: Sánchez-Sánchez F; Martínez-Redondo F; Aroca-Aguilar JD; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Role of MYOC and OPTN sequence variations in Spanish patients with primary open-angle glaucoma.

Molecular vision
2007-06 | Journal article
PMID: 17615537
PMC: PMC2770203
Contributors: Lopez-Martinez F; Lopez-Garrido MP; Sanchez-Sanchez F; Campos-Mollo E; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma.

Human mutation
2007-02 | Journal article
DOI: 10.1002/humu.20394
PMID: 16988938
Contributors: Sánchez-Sánchez F; Ramírez-Castillejo C; Weekes DB; Beneyto M; Prieto F; Nájera C; Mittnacht S
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Sensitivity and specificity of p53 protein detection by immunohistochemistry in patients with urothelial bladder carcinoma.

Urologia internationalis
2007-01 | Journal article
DOI: 10.1159/000109717
PMID: 18025850
Contributors: Salinas-Sánchez AS; Atienzar-Tobarra M; Lorenzo-Romero JG; Sánchez-Sánchez F; Giménez-Bachs JM; Donate-Moreno MJ; Pastor-Navarro H; Escribano-Martínez J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Identification of a lipase-linked cell membrane receptor for pigment epithelium-derived factor.

The Journal of biological chemistry
2006-10 | Journal article
DOI: 10.1074/jbc.m600353200
PMID: 17032652
Contributors: Notari L; Baladron V; Aroca-Aguilar JD; Balko N; Heredia R; Meyer C; Notario PM; Saravanamuthu S; Nueda ML; Sanchez-Sanchez F et al.
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucoma.

Molecular vision
2006-07 | Journal article
PMID: 16862072
Contributors: López-Garrido MP; Sánchez-Sánchez F; López-Martínez F; Aroca-Aguilar JD; Blanco-Marchite C; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

[Promoter hypermethylation status of the mismatch repair gene hMLH1 in patients with sporadic renal cell carcinoma].

Medicina clinica
2006-04 | Journal article
DOI: 10.1157/13086325
PMID: 16620731
Contributors: Salinas-Sánchez AS; Rubio-del-Campo A; Sánchez-Sánchez F; Giménez-Bachs JM; Donate-Moreno MJ; García-Olmo DC; García-Olmo DC; Escribano-Martínez J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Pigment epithelium-derived factor is a niche signal for neural stem cell renewal.

Nature neuroscience
2006-02 | Journal article
DOI: 10.1038/nn1657
PMID: 16491078
Contributors: Ramírez-Castillejo C; Sánchez-Sánchez F; Andreu-Agulló C; Ferrón SR; Aroca-Aguilar JD; Sánchez P; Mira H; Escribano J; Fariñas I
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Determination of vhl gene mutations in sporadic renal cell carcinoma.

European urology
2005-12 | Journal article
DOI: 10.1016/j.eururo.2005.10.028
PMID: 16387411
Contributors: Giménez-Bachs JM; Salinas-Sánchez AS; Sánchez-Sánchez F; Lorenzo-Romero JG; Donate-Moreno MJ; Pastor-Navarro H; García-Olmo DC; García-Olmo DC; Virseda-Rodríguez JA
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Interaction of myocilin with the C-terminal region of hevin.

Biochemical and biophysical research communications
2005-11 | Journal article
DOI: 10.1016/j.bbrc.2005.11.082
PMID: 16316624
Contributors: Li Y; Aroca-Aguilar JD; Ghosh S; Sánchez-Sánchez F; Escribano J; Coca-Prados M
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Relationship between the Arg72Pro polymorphism of p53 and outcome for patients with traumatic brain injury.

Intensive care medicine
2005-07 | Journal article
DOI: 10.1007/s00134-005-2715-0
PMID: 16007417
Contributors: Martínez-Lucas P; Moreno-Cuesta J; García-Olmo DC; Sánchez-Sánchez F; Escribano-Martínez J; del Pozo AC; Lizán-García M; García-Olmo D
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Myocilin mutations causing glaucoma inhibit the intracellular endoproteolytic cleavage of myocilin between amino acids Arg226 and Ile227.

The Journal of biological chemistry
2005-03 | Journal article
DOI: 10.1074/jbc.m501340200
PMID: 15795224
Contributors: Aroca-Aguilar JD; Sánchez-Sánchez F; Ghosh S; Coca-Prados M; Escribano J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

A novel constitutional mutation affecting splicing of retinoblastoma tumor suppressor gene intron 23 causes partial loss of pRB activity.

Human mutation
2005-02 | Journal article
DOI: 10.1002/humu.9305
PMID: 15643604
Contributors: Sánchez-Sánchez F; Kruetzfeldt M; Nájera C; Mittnacht S
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

[Mutational analysis of the vhl gene in the sporadic renal cell carcinoma].

Archivos espanoles de urologia
2004-09 | Journal article
PMID: 15536948
Contributors: Giménez Bachs JM; Salinas Sánchez A; Lorenzo Romero J; Sánchez Sánchez F; Donate Moreno MJ; García Olmo D; Escribano Martínez J; Virseda Rodríguez J
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Polymorphism of Alcohol Dehydrogenase Genes in Alcoholic and Nonalcoholic Individuals from Valencia (Spain)

Hereditas
2004-05-11 | Journal article
DOI: 10.1111/j.1601-5223.1997.00247.x
Part of ISSN: 0018-0661
Contributors: C. Espinós; F. Sánchez; C. Ramírez; F. Juan; C. Nájera
Source: Self-asserted source
Francisco Sánchez Sánchez

p53 Gene mutations in superficial bladder cancer.

Urologia internationalis
2004-01 | Journal article
DOI: 10.1159/000080830
PMID: 15539839
Contributors: Lorenzo Romero JG; Salinas Sánchez AS; Giménez Bachs JM; Sánchez Sánchez F; Escribano Martínez J; Hernández Millán IR; Segura Martín M; Virseda Rodríguez JA
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Prognostic implications of p53 gene mutations in bladder tumors.

The Journal of urology
2003-02 | Journal article
DOI: 10.1097/01.ju.0000046224.57330.70
PMID: 12544295
Contributors: Lorenzo-Romero JG; Salinas-Sánchez AS; Giménez-Bachs JM; Sánchez-Sánchez F; Escribano-Martínez J; Segura-Martín M; Hernandez-Millán IR; Virseda-Rodríguez JA
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Diagnóstico temprano del retinoblastoma: importancia de la búsqueda de mutaciones en el gen RB1

Medicina Clínica
2001-01 | Journal article
DOI: 10.1016/s0025-7753(01)71832-5
Part of ISSN: 0025-7753
Contributors: Carmen Nájera; Francisco Sánchez; Emilia Mateu; Félix Prieto; Magdalena Beneyto
Source: Self-asserted source
Francisco Sánchez Sánchez

A constitutional homozygous mutation in the RB1 gene in a patient with unilateral retinoblastoma

Journal of Medical Genetics
2000-08-01 | Journal article
DOI: 10.1136/jmg.37.8.615
Part of ISSN: 1468-6244
Contributors: F. SANCHEZ
Source: Self-asserted source
Francisco Sánchez Sánchez

Identification of three novel mutations in the MYO7A gene

Human Mutation
1999 | Journal article
DOI: 10.1002/(sici)1098-1004(1999)14:2<181::aid-humu11>3.0.co;2-3
Part of ISSN: 1059-7794
Part of ISSN: 1098-1004
Contributors: Jos� M. Cuevas; C. Espin�s; J.M. Mill�n; F. S�nchez; M.J. Trujillo; C. Ayuso; M. Beneyto; C. N�jera
Source: Self-asserted source
Francisco Sánchez Sánchez

Detection of a novel Cys628STOP mutation of the myosin VIIA gene in Usher syndrome type Ib

Molecular and Cellular Probes
1998-12 | Journal article
DOI: 10.1006/mcpr.1998.0202
Part of ISSN: 0890-8508
Contributors: J.M Cuevas; C Espinós; J.M Millán; F Sánchez; M.J Trujillo; B Garcı́a-Sandoval; C Ayuso; C Nájera; M Beneyto
Source: Self-asserted source
Francisco Sánchez Sánchez

Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome

Human Genetics
1998-07 | Journal article
DOI: 10.1007/s004390050763
Part of ISSN: 0340-6717
Part of ISSN: 1432-1203
Contributors: C. Espinós; J. M. Millán; F. Sánchez; M. Beneyto; C. Nájera
Source: Self-asserted source
Francisco Sánchez Sánchez

Photoperiod-temperature and neuroblast proliferation-migration in the adult lizard cortex.

Neuroreport
1997-07 | Journal article
DOI: 10.1097/00001756-199707070-00047
PMID: 9243636
Contributors: Ramirez C; Nacher J; Molowny A; Sanchez-Sanchez F; Irurzun A; Lopez-Garcia C
Source: Self-asserted source
Francisco Sánchez Sánchez via Europe PubMed Central

Genetics of retinoblastoma: A study

Cancer Genetics and Cytogenetics
1997-05 | Journal article
DOI: 10.1016/s0165-4608(96)00387-1
Part of ISSN: 0165-4608
Contributors: Emilia Mateu; Francisco Sánchez; Carmen Nájera; Magdalena Beneyto; Victoria Castell; Miguel Hernández; Inmaculada Serra; Félix Prieto
Source: Self-asserted source
Francisco Sánchez Sánchez
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