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  • 1-10 ل  55 نتائج ل ""Oligonucleotide""

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Academic Journal

Special Issue "Frontiers in Nucleic Acid Chemistry—In Memory of Professor Enrique Pedroso for His Outstanding Contributions to Nucleic Acid Chemistry".

Subjects: *NUCLEOSIDE synthesis; *OLIGONUCLEOTIDE synthesis; *NUCLEOTIDE synthesisSPAIN

  • Source: Molecules. Nov2023, Vol. 28 Issue 21, p7278. 5p.

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Academic Journal

Characterisation of human outbreaks of brucellosis and sporadic cases by the use of hyper-variable octameric oligonucleotide fingerprint (HOOF) variable number tandem repeats.

Subjects: *DISEASE outbreaks; *BRUCELLA melitensis; *BRUCELLOSISSPAIN

  • Source: Clinical Microbiology & Infection. Sep2007, Vol. 13 Issue 9, p887-892. 6p. 1 Chart, 2 Graphs.

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Conference

Antisense oligonucleotides targeting an oncogenic mitochondrial long non-coding mtRNA to inhibit equine skin tumor cells proliferation

Subjects: Oncology; ASO; Oligonucleotide antisenseSpainBARCELONA, Spain

  • Source: OTS OLIGO MEETING - 19th Annual Meeting ; https://hal.science/hal-04510279 ; OTS OLIGO MEETING - 19th Annual Meeting, 19th Annual Meeting Oligonucleotide Therapeutics

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Academic Journal

A customized pigmentation SNP array identifies a novel SNP associated with melanoma predisposition in the SLC45A2 gene.

  • Authors : Ibarrola-Villava M; Servicio de Oncologia Medica y Hematologia, Fundacion Hospital Clinico Universitario-INCLIVA, Valencia, Spain.; Fernandez LP

Subjects: Genetic Predisposition to Disease* ; Oligonucleotide Array Sequence Analysis* ; Polymorphism, Single Nucleotide*

  • Source: PloS one [PLoS One] 2011 Apr 29; Vol. 6 (4), pp. e19271. Date of Electronic Publication: 2011 Apr 29.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Electronic Cited Medium: Internet

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Academic Journal

Comprehensive SNP-chip for retinitis pigmentosa-Leber congenital amaurosis diagnosis: new mutations and detection of mutational founder effects.

  • Authors : Pomares E; Departament de Genètica, Institut de Biomedicina, Universitat de Barcelona, Barcelona, Spain.; Riera M

Subjects: Founder Effect* ; Oligonucleotide Array Sequence Analysis*; Leber Congenital Amaurosis/Leber Congenital Amaurosis/Leber Congenital Amaurosis/*diagnosis

  • Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2010 Jan; Vol. 18 (1), pp. 118-24.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Identification of loci associated with susceptibility to Mycobacterium avium subsp. paratuberculosis infection in Holstein cattle using combinations of diagnostic tests and imputed whole-genome sequence data.

  • Authors : Canive M; Department of Animal Health, NEIKER- Basque Research and Technology Alliance (BRTA), Derio, Bizkaia, Spain.; Doctoral Program in Immunology, Microbiology and Parasitology, Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU), Leioa, Bizkaia, Spain.

Subjects: Cattle/Cattle/Cattle/*genetics ; Tuberculosis/Tuberculosis/Tuberculosis/*genetics; Animals

  • Source: PloS one [PLoS One] 2021 Aug 27; Vol. 16 (8), pp. e0256091. Date of Electronic Publication: 2021 Aug 27 (Print Publication: 2021).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Human leucocyte antigen ( HLA)- DQB1*03:02 and HLA-A*02:01 have opposite patterns in their effects on susceptibility to HIV infection.

Subjects: ALLELES; CONFIDENCE intervals; DISEASE susceptibilitySPAIN

  • Source: HIV Medicine; Sep2017, Vol. 18 Issue 8, p587-594, 8p

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Academic Journal

Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 Years.

  • Authors : Borobia AM; Clinical Pharmacology Department, IdiPAZ, La Paz University Hospital, School of Medicine, Autonomous University of Madrid, Madrid, Spain.; Dapia I

Subjects: Evidence-Based Medicine/Evidence-Based Medicine/Evidence-Based Medicine/*methods ; Health Plan Implementation/Health Plan Implementation/Health Plan Implementation/*statistics & numerical data ; National Health Programs/National Health Programs/National Health Programs/*statistics & numerical data

  • Source: Clinical and translational science [Clin Transl Sci] 2018 Mar; Vol. 11 (2), pp. 189-199. Date of Electronic Publication: 2017 Nov 28.Publisher: WileyBlackwell Pub Country of Publication: United States NLM ID: 101474067 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders.

  • Authors : Viñas-Jornet M; Genetics lab, UDIAT-centre diagnostic. Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí I3PT. Universitat Autònoma de Barcelona, C/Parc Tauli,1, 08208, Sabadell, Barcelona, Spain.; Cellular Biology, Physiology and Immunology Department, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.

Subjects: DNA Copy Number Variations*; Intellectual Disability/Intellectual Disability/Intellectual Disability/*epidemiology ; Intellectual Disability/Intellectual Disability/Intellectual Disability/*genetics

  • Source: Behavior genetics [Behav Genet] 2018 Jul; Vol. 48 (4), pp. 323-336. Date of Electronic Publication: 2018 Jun 07.Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 0251711 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Prevalence of Rhodopsin mutations in autosomal dominant Retinitis Pigmentosa in Spain: clinical and analytical review in 200 families.

  • Authors : Fernandez-San Jose P; Department of Genetics, Health Research Institute Fundacion Jimenez Diaz, University Hospital (IIS-FJD, UAM), Madrid, Spain; Centre for Biomedical Network Research on Rare Diseases CIBERER, ISCIII, Madrid, Spain.

Subjects: Mutation* ; Polymorphism, Single-Stranded Conformational*; Retinitis Pigmentosa/Retinitis Pigmentosa/Retinitis Pigmentosa/*genetics

  • Source: Acta ophthalmologica [Acta Ophthalmol] 2015 Feb; Vol. 93 (1), pp. e38-44. Date of Electronic Publication: 2014 Nov 18.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101468102 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 ل  55 نتائج ل ""Oligonucleotide""