About: Anna Grandas

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) ഗവേഷക (ml) araştırmacı (tr) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	Anna Grandas (en) Anna Grandas (es) Anna Grandas (nl) Anna Grandas (ast)
skos:prefLabel	Anna Grandas (en) Anna Grandas (es) Anna Grandas (nl) Anna Grandas (ast)
name	Anna Grandas (en) Anna Grandas (es) Anna Grandas (nl) Anna Grandas (ast)
given name	wds:Q41000712-31800EE9-965C-4AC4-BA8F-585E91E73ED3
given name	Anna
instance of	wds:Q41000712-88B7DD92-8D3E-4167-A943-804251F1477A
instance of	Homo sapiens
occupation	wds:Q41000712-95824D79-F90F-4576-B960-A8D7F0052D96
employer	wds:Q41000712-1E2A7020-ECF3-4DB6-B735-230EBC2B32EC
University of Barcelona authority ID	wds:Q41000712-47D489F2-6315-4C5C-9776-036CEE3FA55F
University of Barc...D (former scheme)	wds:Q41000712-8155CC81-717C-4363-9503-979EC431AE16
sex or gender	wds:Q41000712-BC674E30-44CD-488E-BA6C-AA370A06AA33
VIAF ID	wds:Q41000712-ECA47F2A-20FD-4B6C-B83A-E84876433BAB
educated at	wds:Q41000712-7325EDAE-A07F-4602-B846-A4FC5478A5C8 wds:Q41000712-7F055760-C2B4-41CB-9603-CE28D36E3695 wds:Q41000712-D631B8FD-A93A-43C3-967A-201B5FA7B587
WorldCat Identities ID (superseded)	wds:Q41000712-890092E7-C161-4F7F-A496-7A3EF0C2A5E7
CANTIC ID	wds:Q41000712-46630120-FF3F-464B-86AC-30EBFCCE00E0
VIAF ID	http://viaf.org/viaf/305873182
occupation	researcher
employer	University of Barcelona
University of Barcelona authority ID	981058509875306706
University of Barc...D (former scheme)	a1019985
sex or gender	female organism
VIAF ID	305873182
educated at	University of Colorado Boulder University of Barcelona
WorldCat Identities ID (superseded)	viaf-305873182
CANTIC ID	981058509875306706
ORCID iD	wds:Q41000712-CFA3B5BE-6373-4F92-81CF-98D07CF95EA1
ORCID iD	https://orcid.org/0000-0001-6517-4018
ORCID iD	0000-0001-6517-4018
ResearcherID	wds:Q41000712-C511F744-AB21-44A6-902A-1A8B88DDEA29
Publons author ID	wds:Q41000712-bc7c567e-d570-4e94-bfd1-fa57799f3211
ResearcherID	K-6419-2014
Publons author ID	1643891
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q41000712
is author of	Binding affinities of oligonucleotides and PNAs containing phenoxazine and G-clamp cytosine analogues are unusually sequence-dependent. Convergent solid phase peptide synthesis. VII. Good yields in the coupling of protected segments on a solid support Diketopiperazine formation in solid phase peptide synthesis using p-alkoxybenzyl ester resins and Fmoc-amino acids Processing of nucleopeptides mimicking the topoisomerase I-DNA covalent complex by tyrosyl-DNA phosphodiesterase Compensatory effects of the human nucleoside transporters on the response to nucleoside-derived drugs in breast cancer MCF7 cells. Insights into the reaction of transplatin with DNA and proteins: methionine-mediated formation of histidine-guanine trans-Pt(NH3)2 cross-links AN IMPROVED SYNTHESIS OF N-[(9-HYDROXYMETHYL)-2-FLUORENYL]SUCCINAMIC ACID (HMFS), A VERSATILE HANDLE FOR THE SOLID-PHASE SYNTHESIS OF BIOMOLECULES Incorporation of two modified nucleosides allows selective platination of an oligonucleotide making it suitable for duplex cross-linking Selective Platination of Modified Oligonucleotides and Duplex Cross-Links Solution structure and stability of tryptophan-containing nucleopeptide duplexes Stabilization of DNA duplexes by covalently-linked peptides Multivariate Curve Resolution Applied to the Analysis and Resolution of Two-Dimensional [1H,15N] NMR Reaction Spectra Identification of Ligands for the Tau Exon 10 Splicing Regulatory Element RNA by Using Dynamic Combinatorial Chemistry Design and DNA binding of an extended triple-stranded metallo-supramolecular cylinder. Towards nucleopeptides containing any trifunctional amino acid (II) Towards a better understanding of the cisplatin mode of action Fast atom bombardment mass spectrometry of protected peptide segments Convergent solid phase peptide synthesis. I. Synthesis of protected segments on a hydroxymethylphenyloxymethyl resin using the base labile FMOC α-amine protection. Model synthesis of LHRH Exploiting protected maleimides to modify oligonucleotides, peptides and peptide nucleic acids. Oligonucleotide cyclization: the thiol-maleimide reaction revisited Orthogonal Protection of Peptides and Peptoids for Cyclization by the Thiol–Ene Reaction and Conjugation Protected Maleimide Building Blocks for the Decoration of Peptides, Peptoids, and Peptide Nucleic Acids Straightforward Synthesis of Cyclic and Bicyclic Peptides Conjugation Reactions Involving Maleimides and Phosphorothioate Oligonucleotides Easy introduction of maleimides at different positions of oligonucleotide chains for conjugation purposes Maleimide-DimethylfuranexoAdducts: Effective Maleimide Protection in the Synthesis of Oligonucleotide Conjugates Mammalian frataxin directly enhances sulfur transfer of NFS1 persulfide to both ISCU and free thiols Local RNA flexibility perturbation of the IRES element induced by a novel ligand inhibits viral RNA translation Towards nucleopeptides containing any trifunctional amino acid Electron paramagnetic resonance (EPR) study of spin-labeled camptothecin derivatives: a different look of the ternary complex.

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