Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Antonio Coloma"'
Publikováno v:
Innovación y Software, Vol 3, Iss 2, Pp 6-25 (2022)
El artículo evidencia la implementación de una aplicación móvil para la gestión de información sobre el consumo del líquido vital en los hogares que conforman la junta administradora de agua potable de la parroquia Santa Fe, tal sistema inform
Externí odkaz:
https://doaj.org/article/309faf43ddb84b5c9062e500e9c337b0
Autor:
Jesús Cruces, Adriana Izquierdo-Lahuerta, Francisco Gómez-Esquer, Oscar de Luis, Antonio Coloma
Publikováno v:
Biochemical and biophysical research communications. 478(3)
Alpha-dystroglycanopathies are a heterogenic group of human rare diseases that have in common defects of α-dystroglycan O-glycosylation. These congenital disorders share common features as muscular dystrophy, malformations on central nervous system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33df18814a0ebe18519334496854ef4
https://pubmed.ncbi.nlm.nih.gov/27553274
https://pubmed.ncbi.nlm.nih.gov/27553274
Publikováno v:
Genomics. 58:171-180
We have isolated a human gene homologous to Drosophila melanogaster rotated abdomen, rt, a poorly viable recessive mutation causing a clockwise twisted abdomen in affected flies due to defects in embryonic muscle development. The human gene, like rt,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0494a463ca03455774f3de386ccbdbfc
https://doi.org/10.1006/geno.1999.5819
https://doi.org/10.1006/geno.1999.5819
Publikováno v:
Endocrinology. 140:335-343
NRGN is the human homolog of the neuron-specific rat RC3/neurogranin gene. This gene encodes a postsynaptic 78-amino acid protein kinase substrate that binds calmodulin in the absence of calcium, and that has been implicated in dendritic spine format
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5550f42630bf674e39026f51f431dda4
https://doi.org/10.1210/endo.140.1.6461
https://doi.org/10.1210/endo.140.1.6461
Publikováno v:
Human Molecular Genetics. 7:325-334
Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder with multisystemic manifestations caused by heterozygosity for a partial deletion of chromosome band 7q11.23. The breakpoints cluster within regions located approximately 1 cM either sid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf56df163c2594ffef8535fb26f15e8d
https://doi.org/10.1093/hmg/7.3.325
https://doi.org/10.1093/hmg/7.3.325
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1263:45-52
The genes encoding the acidic ribosomal phosphoproteins DdP1 and DdP2 from Dictyostelium discoideum have been cloned into yeast plasmid vectors under the control of the inducible GAL1 promoter. These constructions have been used to transform S. cerev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0267d24391277b369139b85c75ac9d90
https://doi.org/10.1016/0167-4781(95)00081-q
https://doi.org/10.1016/0167-4781(95)00081-q
Autor:
Melanie M. Mahtani, Ilkka Kaitila, Greg Clines, Albert de la Chapelle, Michael Lovett, Eric S. Lander, Mary Pat Reeve-Daly, J. Hästbacka, Bruce A. Hamilton, Bijal Trivedi, Mark J. Daly, Alan Buckler, Alix Weaver, Kenro Kusumi, Antonio Coloma
Publikováno v:
Cell. 78:1073-1087
Diastrophic dysplasia (DTD) is a well-characterized autosomal recessive osteochondrodysplasia with clinical features including dwarfism, spinal deformation, and specific joint abnormalities. The disease occurs in most populations, but is particularly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::781d26bde2aa24104fb1292fc43262d5
https://doi.org/10.1016/0092-8674(94)90281-x
https://doi.org/10.1016/0092-8674(94)90281-x
Autor:
Miguel A. F. Sanjuán, Adriana Izquierdo, Alexandre Wagemakers, Antonio Coloma, Oscar de Luis, Javier M. Buldú
Publikováno v:
Chaos (Woodbury, N.Y.). 19(3)
We propose a new approach for synchronizing a population of synthetic genetic oscillators, which consists in the entrainment of a colony of repressilators by external modulation. We present a model where the repressilator dynamics is affected by peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::418457228b2ef208164d3e7f12e7de1c
https://pubmed.ncbi.nlm.nih.gov/19792019
https://pubmed.ncbi.nlm.nih.gov/19792019
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1115:6-14
Four acidic phosphoproteins from the ribosomes of the slime mold Dictyostelium discoideum have been identified and partially characterized. These proteins are selectively released from ribosomal particles by salt/ethanol washes, have low molecular we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f79ffb111e283a7eb9885da151438e0e
https://doi.org/10.1016/0304-4165(91)90004-z
https://doi.org/10.1016/0304-4165(91)90004-z
Autor:
Martin Hrabé de Angelis, Mark Lommel, Jesús Cruces, Juan M. Falcón-Pérez, Eckhard Wolf, Tobias Willer, Ingrid Renner-Müller, Widmar Tanner, Gerhard K. H. Przemeck, Antonio Coloma, Belén Prados, Sabine Strahl, M. Carmen Valero
Publikováno v:
Proc. Natl. Acad. Sci. U.S.A. 101, 14126-14131 (2004)
O-mannosylation is an important protein modification in eukaryotes that is initiated by an evolutionarily conserved family of protein O -mannosyltransferases. The first mammalian protein O -mannosyltransferase gene described was the human POMT1 . Mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f72396f246d8fa0492a25c73719973eb
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=4597
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=4597
