about
Identification, expression and chromosome localization of a human gene encoding a novel protein with similarity to the pilB family of transcriptional factors (pilin) and to bacterial peptide methionine sulfoxide reductasescDNA from human ocular ciliary epithelium homologous to beta ig-h3 is preferentially expressed as an extracellular protein in the corneal epitheliumLocation and characterization of the three carbohydrate prosthetic groups of human protein HCIdentification of a lipase-linked cell membrane receptor for pigment epithelium-derived factorCrocin, safranal and picrocrocin from saffron (Crocus sativus L.) inhibit the growth of human cancer cells in vitroIsolation and characterization of cell-specific cDNA clones from a subtractive library of the ocular ciliary body of a single normal human donor: transcription and synthesis of plasma proteinsNew perspectives in aqueous humor secretion and in glaucoma: the ciliary body as a multifunctional neuroendocrine glandHypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variabilityPrognostic implications of p53 gene mutations in bladder tumors.Sensitivity and specificity of p53 protein detection by immunohistochemistry in patients with urothelial bladder carcinoma.Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development.Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucomaBicarbonate-dependent secretion and proteolytic processing of recombinant myocilinInteraction of recombinant myocilin with the matricellular protein SPARC: functional implicationsWDR36 and P53 gene variants and susceptibility to primary open-angle glaucoma: analysis of gene-gene interactions.LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients.Cloning and characterization of subtracted cDNAs from a human ciliary body library encoding TIGR, a protein involved in juvenile open angle glaucoma with homology to myosin and olfactomedin.Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.CYP1B1 mutations in Spanish patients with primary congenital glaucoma: phenotypic and functional variability.Recent patents and developments in glaucoma biomarkers.Comparative proteomic study in serum of patients with primary open-angle glaucoma and pseudoexfoliation glaucoma.Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes.GSTT1, GSTM1, and CYP1B1 gene polymorphisms and susceptibility to sporadic renal cell cancer.Functional analysis of CYP1B1 mutations and association of heterozygous hypomorphic alleles with primary open-angle glaucoma.Expression and purification of functional recombinant human pigment epithelium-derived factor (PEDF) secreted by the yeast Pichia pastoris.Characterization of the intracellular proteolytic cleavage of myocilin and identification of calpain II as a myocilin-processing protease.Molecular and neurochemical substrates of the audiogenic seizure strains: The GASH:Sal model.CFH polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration.Sex steroid hormone metabolism takes place in human ocular cells.Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing.Polymorphic deletions of the GSTT1 and GSTM1 genes and susceptibility to bladder cancer.Opposite caudal versus rostral brain nitric oxide synthase response to generalized seizures in a novel rodent model of reflex epilepsy.Primary congenital glaucoma caused by the homozygous F261L CYP1B1 mutation and paternal isodisomy of chromosome 2.Relationship between the Arg72Pro polymorphism of p53 and outcome for patients with traumatic brain injury.MYOC gene mutations in Spanish patients with autosomal dominant primary open-angle glaucoma: a founder effect in southeast Spain.Spectroscopic characterization by photodiode array detection of human urinary and amniotic protein HC subpopulations fractionated by anion-exchange and size-exclusion high-performance liquid chromatography.Pigment epithelium-derived factor is a niche signal for neural stem cell renewal.Metallothionein polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration.Using ankle-brachial index to detect peripheral arterial disease: prevalence and associated risk factors in a random population sample.Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Julio Escribano
@ast
Julio Escribano
@en
Julio Escribano
@es
Julio Escribano
@nl
Julio Escribano
@sl
type
label
Julio Escribano
@ast
Julio Escribano
@en
Julio Escribano
@es
Julio Escribano
@nl
Julio Escribano
@sl
altLabel
Julio Escribano-Martínez
@en
prefLabel
Julio Escribano
@ast
Julio Escribano
@en
Julio Escribano
@es
Julio Escribano
@nl
Julio Escribano
@sl
P1053
D-9742-2015
P106
P1153
35518550700
P21
P31
P3829
P496
0000-0002-8919-8134