Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Manuela Jay"'
Publikováno v:
Iatreia, Vol 23, Iss 4-S (2010)
La literatura mundial ha reportado más de 100 enfermedades neurodegenerativas relacionadas con errores innatos del metabolismo que presentan un amplia expresión fenotípica, una de ellas es la enfermedad de Krabbe (EK), desorden genético autosómi
Externí odkaz:
https://doaj.org/article/e5e5d36c670649de8d936e579e3e8fed
Autor:
Tatiana Castillo, Annabelle Trojan, Maria Claudia Noguera, Lina Manuela Jay, Cecilia Crane, Alexander Shevelev, Alvaro Alvarez, Heliodor Kasprzak, Gonzalo Melo, Pedro Jose Penagos, Beatriz Helena Aristizabal, Ignacio Briceño, Adis Ayala, Huynh T. Duc, Jerzy Trojan
Publikováno v:
Revista Científica, Vol 2, Iss 25, Pp 228-240 (2016)
We have been faced with a 40 year long challenge: how to establish tools that can be applied in the treatment of brain tumor - glioblastoma (100% fatal) - using our knowledge of evolution, chemistry of proteins, genetics, molecular biology and immuno
Externí odkaz:
https://doaj.org/article/95c04fbb25b9426180c27b4eb3e78201
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
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
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
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
Publikováno v:
Journal of Cancer Therapy. :685-705
The review article describes the criteria established for methodology of antisense anti IGF-I therapy of malignant tumors, particularly of glioblastoma. The cancer patients, after classical therapy of surgery, radiotherapy and chemotherapy, have unde
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
Autor:
Gonzalo Melo, Adis Ayala, Maria Claudia Noguera, H.T. Duc, Annabelle Trojan, Heliodor Kasprzak, Jerzy Trojan, Pedro Penagos, Alvaro Alvarez, A. Shevelev, Tatiana Castillo, Lina Manuela Jay, Ignacio Briceño, Cecilia Crane, Beatriz H. Aristizabal
Publikováno v:
Revista Científica. 2:228
Unos de los retos científicos de los últimos 40 años, ha sido la búsqueda de la herramienta para el tratamiento del tumor cerebral, el glioblastoma, mortales en el 100% de los casos, utilizando nuestro conocimiento de la evolución, la química d
Autor:
Tatiana Castillo, Annabelle Trojan, Pedro Penagos, Beatriz H. Aristizabal, Jerzy Trojan, Lina Manuela Jay, Ignacio Briceño
Publikováno v:
Advances in Modern Oncology Research, Vol 2, Iss 4, Pp 188-200 (2016)
As we have come to know, there is a connection between cancer biomarkers and genes, along with their susceptibility to a particular disease, all of which have an obvious impact on the clinical practice and development of genetic testing. In any cance