Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lina Manuela Jay Garcia"'
Autor:
Margaret Murphy, Quincy L Faber, Lina Manuela Jay-Garcia, Katherine A Rees, Yury O. Chernoff, Denis A. Kiktev, Numera Sachwani, Rebecca L. Howie
Publikováno v:
Genetics. 212:757-771
Self-perpetuating protein aggregates (prions) cause diseases in mammals. Yeast prions are heritable in cell divisions. Howie et al. demonstrate that the cellular apparatus responsible for the asymmetry of cell division controls destabilization of a y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4651ae0d4f7bbba5aaf261df125d75af
https://doi.org/10.1534/genetics.119.302237
https://doi.org/10.1534/genetics.119.302237
Autor:
Lina Manuela Jay-Garcia, Andrew G. Matveenko, Yury O. Chernoff, Galina A. Zhouravleva, Yury A. Barbitoff
Publikováno v:
Current Genetics. 64:317-325
Endogenous yeast amyloids that control heritable traits and are frequently used as models for human amyloid diseases are termed yeast prions. Yeast prions, including the best studied ones ([PSI +] and [URE3]), propagate via intimate interactions with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7699e7f70dda1125b92246c7f577e1c1
https://doi.org/10.1007/s00294-017-0750-3
https://doi.org/10.1007/s00294-017-0750-3
Publikováno v:
Revista Med. 25:7-19
Krabbe disease is a disorder of autosomal recessive sphingolipid metabolism caused by deficiency β-galactosylceramidase (β-Galsil) (EC3.2.1.46), an enzymatic defect that causes a hurt neurodegenerative, muscular hypertonia and Spasticity, convulsio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a033619a24e724b6e410fb283358d809
https://doi.org/10.18359/rmed.2875
https://doi.org/10.18359/rmed.2875
Autor:
Rebecca L, Howie, Lina Manuela, Jay-Garcia, Denis A, Kiktev, Quincy L, Faber, Margaret, Murphy, Katherine A, Rees, Numera, Sachwani, Yury O, Chernoff
Publikováno v:
Genetics
Self-perpetuating transmissible protein aggregates, termed prions, are implicated in mammalian diseases and control phenotypically detectable traits in Saccharomyces cerevisiae. Yeast stress-inducible chaperone proteins, including Hsp104 and Hsp70-Ss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccf98988b5f057b8c03fb08cb9add7df
https://pubmed.ncbi.nlm.nih.gov/31142614
https://pubmed.ncbi.nlm.nih.gov/31142614
Autor:
Isidro Arevalo, Adis Ayala, Natalia Pacheco, Lina Manuela Jay Garcia, Monica España, Alfredo Uribe
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening v.3 2015
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
β-Galactosidase (BGal) is the first enzyme involved in the catabolism of sphingolipids. Two pathologies have been directly associated with its deficiency: GM1 gangliosidosis and Morquio B. Morquio B is among the rarest types of mucopolysaccharidosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::645533543a258df816ab1305962fb50b
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942015000100353
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942015000100353
