Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sylvia Balabanian"'
Publikováno v:
Neurological Research. 29:413-424
Spinal muscular atrophy (SMA) is caused by survival of motor neuron (SMN) deficiency, leading to specific motor neuron attrition. The time course and molecular pathophysiologic etiology of motor neuron loss observed in SMA remains obscure. Mice heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4655541d9beb528602400fe833f10e7e
https://doi.org/10.1179/016164107x159243
https://doi.org/10.1179/016164107x159243
Publikováno v:
Human molecular genetics. 18(21)
Spinal muscle atrophy (SMA) is an autosomal recessive neurodegenerative disease which is characterized by the loss of alpha motor neurons resulting in progressive muscle atrophy. Reduced amount of functional survival motor neuron (SMN) protein due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e172fa560029814ff1eddb10adc3a7db
https://pubmed.ncbi.nlm.nih.gov/19648294
https://pubmed.ncbi.nlm.nih.gov/19648294
Autor:
Nathalie H. Gendron, Alex MacKenzie, Sylvia Balabanian, Cynthia R. Coffill, Douglas J. Franks, Alexandra Stewart, Louise Pelletier, Johannes K. X. Maier
Publikováno v:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society. 55(9)
The neuronal apoptosis inhibitory protein (NAIP) gene, also known as the baculovirus inhibitor of apoptosis repeat-containing protein 1 (BIRC1) gene, is a member of the inhibitors of apoptosis (IAP) family and was first characterized as a candidate g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234c629df31bd54abbdb81f4338e2358
https://pubmed.ncbi.nlm.nih.gov/17510375
https://pubmed.ncbi.nlm.nih.gov/17510375
Publikováno v:
Neurological Research; Jul2007, Vol. 29 Issue 5, p413-424, 12p, 1 Black and White Photograph, 2 Diagrams, 3 Charts, 1 Graph
Publikováno v:
Assay & Drug Development Technologies; Dec2005, Vol. 3 Issue 6, p715-726, 12p