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  1. Zebrafishadamtsl4knockout recapitulates key features of humanADAMTSL4-related diseases: a gene involved in extracellular matrix organization, cell junctions and development
  2. The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease
  3. Primary congenital glaucoma in two siblings with different compound heterozygous CYP1B1 genotypes
  4. The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease
  5. Seizures regulate the cation-Cl− cotransporter NKCC1 in a hamster model of epilepsy: implications for GABA neurotransmission
  6. Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish
  7. Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish
  8. RNA and protein expression analysis of HLA‐DQB1*03:01:01:21Q allele: A null allele renamed as HLA‐DQB1*03:01:01:21N ...
  9. Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes
  10. Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes
  11. Knockout of myoc Provides Evidence for the Role of Myocilin in Zebrafish Sex Determination Associated with Wnt Signalling Downregulation
  12. Knockout of myoc reveals the role of myocilin in zebrafish sex determination associated with Wnt signalling downregulation
  13. Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish
  14. CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
  15. Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish
  16. Current perspectives in Bietti crystalline dystrophy
  17. Transforming growth factor beta‐induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients
  18. Cataract extraction in patients with primary congenital glaucoma
  19. Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma
  20. Identification of myocilin as a blood plasma protein and analysis of its role in leukocyte adhesion to endothelial cell monolayers
  21. Identification of novel CYP4V2 genotypes associated with Bietti crystalline dystrophy and atypical anterior segment phenotypes in Spanish patients
  22. Informing the Transitions towards Low-carbon Societies
  23. Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma
  24. Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development
  25. Metallothionein polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration
  26. A novel transient phase kinetic analysis of the fractional modification of monocyclic enzyme cascades
  27. Functional characterization of eight rare missenseCYP1B1variants involved in congenital glaucoma and their association with null genotypes
  28. The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 Mutations
  29. LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients
  30. Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
  31. CFHpolymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration
  32. Molecular and neurochemical substrates of the audiogenic seizure strains: The GASH:Sal model
  33. Hypo- and Hypermorphic FOXC1 Mutations in Dominant Glaucoma: Transactivation and Phenotypic Variability
  34. Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations
  35. Analysis of the fractional modification of the monocyclic enzyme cascades, defined in an alternative way involving the two forms of the modified protein
  36. Comparative proteomic study in serum of patients with primary open-angle glaucoma and pseudoexfoliation glaucoma
  37. Genotype–Phenotype Analysis of Bietti Crystalline Dystrophy in a Family with the CYP4V2 Ile111Thr Mutation
  38. Co‐inheritance of HNF1a and GCK mutations in a family with maturity‐onset diabetes of the young (MODY): implications for genetic testing
  39. Null CYP1B1 Genotypes in Primary Congenital and Nondominant Juvenile Glaucoma
  40. Bicarbonate-Dependent Secretion and Proteolytic Processing of Recombinant Myocilin
  41. GSTT1, GSTM1, and CYP1B1 gene polymorphisms and susceptibility to sporadic renal cell cancer
  42. Recent Patents and Developments in Glaucoma Biomarkers
  43. Opposite caudal versus rostral brain nitric oxide synthase response to generalized seizures in a novel rodent model of reflex epilepsy
  44. Role of CYP1B1 Gene Polymorphisms in Bladder Cancer Susceptibility
  45. Triterpenoid saponins from corms of Crocus sativus: Localization, extraction and characterization
  46. WDR36andP53Gene Variants and Susceptibility to Primary Open-Angle Glaucoma: Analysis of Gene-Gene Interactions
  47. Importance of clinical variables in the diagnosis of MODY2 and MODY3
  48. Importance of clinical variables in the diagnosis of MODY2 and MODY3
  49. Interaction of Recombinant Myocilin with the Matricellular Protein SPARC: Functional Implications
  50. Genética del glaucoma: la luz al final del túnel catorce años después
  51. Polymorphic deletions of the GSTT1 and GSTM1 genes and susceptibility to bladder cancer
  52. A general model for non-autocatalytic zymogen activation in the presence of two different and mutually exclusive inhibitors. I. Kinetic analysis
  53. A general model for non-autocatalytic zymogen activation in the presence of two different and mutually exclusive inhibitors. II. Relative weight of activation and inhibition processes
  54. Functional Role of Proteolytic Processing of Recombinant Myocilin in Self-Aggregation
  55. Clinical differences between patients with MODY-3, MODY-2 and type 2 diabetes mellitus with I27L polymorphism in the HNF1α gene
  56. Functional analysis ofCYP1B1mutations and association of heterozygous hypomorphic alleles with primary open-angle glaucoma
  57. Primary congenital glaucoma caused by the homozygous F261LCYP1B1mutation and paternal isodisomy of chromosome 2
  58. Implications of p53 gene mutations on patient survival in transitional cell carcinoma of the bladder: A long-term study
  59. Implications of mismatch repair genes hMLH1and hMSH2in patients with sporadic renal cell carcinoma
  60. Expression and purification of functional recombinant human pigment epithelium-derived factor (PEDF) secreted by the yeast Pichia pastoris
  61. VHL Protein Alterations in Sporadic Renal Cell Carcinoma
  62. Mental Health and Functional Outcomes of Maternal and Adolescent Reports of Adolescent Depressive Symptoms
  63. Characterization of the Intracellular Proteolytic Cleavage of Myocilin and Identification of Calpain II as a Myocilin-processing Protease
  64. New perspectives in aqueous humor secretion and in glaucoma: The ciliary body as a multifunctional neuroendocrine gland
  65. Sensitivity and Specificity of P53 Protein Detection by Immunohistochemistry in Patients with Urothelial Bladder Carcinoma
  66. Using ankle-brachial index to detect peripheral arterial disease: Prevalence and associated risk factors in a random population sample
  67. Kinetic analysis of a general model of activation of aspartic proteinase zymogens involving a reversible inhibitor. II. Contribution of the uni- and bimolecular activation routes
  68. Identification of a Lipase-linked Cell Membrane Receptor for Pigment Epithelium-derived Factor
  69. Determination of vhl Gene Mutations in Sporadic Renal Cell Carcinoma
  70. Hipermetilación del promotor del gen reparador hMLH1 en la patogenia del carcinoma de células renales esporádico
  71. Pigment epithelium–derived factor is a niche signal for neural stem cell renewal
  72. Interaction of myocilin with the C-terminal region of hevin
  73. Relationship between the Arg72Pro Polymorphism of p53 and outcome for patients with traumatic brain injury
  74. Myocilin Mutations Causing Glaucoma Inhibit the Intracellular Endoproteolytic Cleavage of Myocilin between Amino Acids Arg226 and Ile227
  75. DEVELOPMENT AND GENE EXPRESSION IN SAFFRON CORMS
  76. PRESENCE OF BIOACTIVE GLYCOCONJUGATES ON DIFFERENT STAGES OF SAFFRON CORM
  77. p53 Gene Mutations in Superficial Bladder Cancer
  78. Sex steroid hormone metabolism takes place in human ocular cells
  79. Prognostic Implications of p53 Gene Mutations in Bladder Tumors
  80. Identification of a Neuropeptide and Neuropeptide-Processing Enzymes in Aqueous Humor Confers Neuroendocrine Features to the Human Ocular Ciliary Epithelium
  81. Comparison of three different PCR methods for detection of Brucella spp. in human blood samples
  82. Threonines at position 174 and 235 of the angiotensinogen polypeptide chain are related to familial history of hypertension in a Spanish-Mediterranean population
  83. Expression of the TIGR gene in the iris, ciliary body, and trabecular meshwork of the human eye
  84. A glycoconjugate from corms of saffron plant (Crocus sativus L.) inhibits root growth and affects in vitro cell viability
  85. A glycoconjugate from corms of saffron plant ( Crocus sativus L.) inhibits root growth and affects in vitro cell viability
  86. The Cytolytic Effect of a Glycoconjugate Extracted from Corms of Saffron Plant (Crocus sativus) on Human Cell Lines in Culture
  87. Purification and Characterization of a Mannan-Binding Lectin Specifically Expressed in Corms of Saffron Plant ( Crocus s ativus L.)
  88. Angiotensin-converting enzyme (ACE) gene polymorphisms, serum ACE activity and blood pressure in a Spanish-Mediterranean population
  89. A Glycoconjugate Isolated from the Saffron Plant (Crocus sativus L.) is Cytolytic Against Tumoral Cells and Activates Macrophages In Vitro
  90. A Proteoglycan from Saffron Corm (Crocus sativus L.) Inhibits Root Elongation of Nicotiana tabacum Seedlings and is Highly Cytotoxic on Tobacco Cells and Protoplasts
  91. Expression of the TIGR gene in the iris, ciliary body, and trabecular meshwork of the human eye
  92. Effects of Long-Term Treatment of Colon Adenocarcinoma With Crocin, a Carotenoid From Saffron (Crocus sativus L.): An Experimental Study in the Rat
  93. In vitro activation of macrophages by a novel proteoglycan isolated from corms of Crocus sativus L
  94. Differential gene expression in the human ciliary epithelium
  95. Production of a cytotoxic proteoglycan using callus culture of saffron corms (Crocus sativus L.)
  96. 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 reductases
  97. PCR Assay for Diagnosis of Human Brucellosis
  98. Associated evaluation of differents variants of Angiotensinogen gen and the relation with blood pressure levels. Results of an epidemiologic study
  99. Relationship between variants of AT1R gene with blood pressure levels in a spanish population. Results of an epidemiologic study
  100. Isolation and cytotoxic properties of a novel glycoconjugate from corms of saffron plant (Crocus sativus L.)
  101. Development of cormogenic nodules and microcorms by tissue culture, a new tool for the multiplication and genetic improvement of saffron
  102. Genetics of hypertension in a Spanish population. Results from epidemiologic study, with a case-control population-based design
  103. 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
  104. Gene Expression of Proteases and Protease Inhibitors in the Human Ciliary Epithelium and ODM-2 Cells
  105. Treatment of human brucellosis with doxycycline and gentamicin.
  106. Crocin, safranal and picrocrocin from saffron (Crocus sativus L.) inhibit the growth of human cancer cells in vitro
  107. 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
  108. Isolation 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 Proteins
  109. cDNA from human ocular ciliary epithelium homologous to ?ig-h3 is preferentially expressed as an extracellular protein in the corneal epithelium
  110. Efficient thyroid hormone formation by in vitro iodination of a segment of rat thyroglobulin fused to Staphylococcal protein A
  111. Identification of peptides containing aromatic amino acids, cysteine, iodotyrosine and iodothyronine by high-performance liquid chromatography with photodiode-array detection
  112. Location and characterization of the three carbohydrate prosthetic groups of human protein HC
  113. Direct Characterization of Proteins and Peptides in HPLC by Photodiode Array UV-VIS Detection: A New Approach in the Detection and Characterization of Polypeptides
  114. Identification of retinol as one of the protein HC chromophores
  115. High-performance liquid chromatography and photodiode-array detection of the human protein HC (human complex-forming glycoprotein heterogeneous in charge), a chromophore-associated protein