about
Identification and structural and functional characterization of human enamelysin (MMP-20)Testis-specific transcripts of rat farnesyl pyrophosphate synthetase are developmentally regulated and localized to haploid germ cellsA missense mutation in Tbce causes progressive motor neuronopathy in miceAssociation of the mouse infertility factor DAZL1 with actively translating polyribosomes.Isolation and characterization of XE169, a novel human gene that escapes X-inactivation.Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome.Epidemiologic genotyping of methicillin-resistant Staphylococcus aureus by pulsed-field gel electrophoresis at a university hospital and comparison with antibiotyping and protein A and coagulase gene polymorphisms.Expression of epidermal growth factor in the rat kidney. An immunocytochemical and in situ hybridization study.Cancer modifier alleles inhibiting lung tumorigenesis are common in inbred mouse strains.Expression of epidermal growth factor in the kidney and submandibular gland during mouse postnatal development. An immunocytochemical and in situ hybridization study.Expression of the X-inactivation-associated gene XIST during spermatogenesis.Expression of steroid sulfatase during embryogenesis.Molecular therapy of primary hyperoxaluria.Genetic mapping of the adenine nucleotide translocase-2 gene (Ant2) to the mouse proximal X chromosome.The murine Xe169 gene escapes X-inactivation like its human homologue.Tumour spectrum of non-polyposis colorectal cancer (Lynch syndrome) on the island of Tenerife and influence of insularity on the clinical manifestations.High frequency de novo alterations in the long-range genomic structure of the mouse pseudoautosomal region.Human papillomavirus-associated penile squamous cell carcinoma in HIV-positive patients.A new locus for resistance to gamma-radiation-induced thymic lymphoma identified using inter-specific consomic and inter-specific recombinant congenic strains of mice.Evolutionary Divergent Suppressor Mutations in Conformational DiseasesCRISPR/Cas9-mediated glycolate oxidase disruption is an efficacious and safe treatment for primary hyperoxaluria type ISalicylic Acid Derivatives Inhibit Oxalate Production in Mouse Hepatocytes with Primary Hyperoxaluria Type 1Lack of prenatal testosterone surge in fetal rats exposed to alcohol: alterations in testicular morphology and physiologyNerve growth factor immunoreactivity in mouse kidney: an immunoelectron microscopic studyImmunoelectron microscopy of epidermal growth factor in mouse kidneyImmunocytochemical localization of nerve growth factor in mouse kidneyLymphangioma of the duodenum: an ultrastructural studyExpression of epidermal growth factor receptor (proto-oncogene c-erbB-1) and estrogen receptor in human breast carcinoma. An immunocytochemical study of 70 casesInfluence of vitamin D receptor genotype on bone mass changes after renal transplantationHigh phosphorus diet increases preproPTH mRNA independent of calcium and calcitriol in normal ratsAmelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfectaVitamin D receptor gene polymorphisms, bone mass, bone loss and prevalence of vertebral fracture: differences in postmenopausal women and menPrediction of left ventricular mass changes after renal transplantation by polymorphism of the angiotensin-converting-enzyme geneThe distribution of two different vitamin D receptor polymorphisms (BsmI and start codon) in primary hyperparathyroidismThe ACE/DD genotype is associated with the extent of exercise-induced left ventricular growth in endurance athletesVitamin D receptor genotype: its role in bone mass and turnover in non-renal and renal patientsRegression of left ventricular hypertrophy by lisinopril after renal transplantation: role of ACE gene polymorphismDietary fish oil does not influence acute rejection rate and graft survival after renal transplantation: a randomized placebo-controlled study
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P50
description
researcher, ORCID id # 0000-0001-9599-9854
@en
wetenschapper
@nl
name
Eduardo Salido
@ast
Eduardo Salido
@en
Eduardo Salido
@es
Eduardo Salido
@nl
type
label
Eduardo Salido
@ast
Eduardo Salido
@en
Eduardo Salido
@es
Eduardo Salido
@nl
prefLabel
Eduardo Salido
@ast
Eduardo Salido
@en
Eduardo Salido
@es
Eduardo Salido
@nl
P106
P21
P31
P496
0000-0001-9599-9854