Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marı́a T Berciano"'
Autor:
Nuria T Villagrá, José Berciano, Marcos Altable, Joaquı́n Navascués, Iñigo Casafont, Miguel Lafarga, Marı́a T Berciano
Publikováno v:
Neurobiology of Disease, Vol 16, Iss 1, Pp 158-168 (2004)
Acute inflammatory demyelinating polyneuropathy (AIDP) is a type of Guillain–Barré syndrome (GBS) characterized by primary nerve demyelination sometimes with secondary axonal degeneration. Studies on the fine structure of dorsal root ganglia in AI
Externí odkaz:
https://doaj.org/article/dac1c8243c8f4f14bf7330386eb0defc
Autor:
Sonia Brun, Neus Abella, Maria T Berciano, Olga Tapia, Montserrat Jaumot, Raimundo Freire, Miguel Lafarga, Neus Agell
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0178925 (2017)
We previously showed that p21Cip1 transits through the nucleolus on its way from the nucleus to the cytoplasm and that DNA damage inhibits this transit and induces the formation of p21Cip1-containing intranucleolar bodies (INoBs). Here, we demonstrat
Externí odkaz:
https://doaj.org/article/f610d724676444bf8137644f458fc2ba
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive weakness and muscle atrophy related to the loss of upper and lower motor neurons (MNs) without a curative treatment. There is experimental evidence sugges
Externí odkaz:
https://doaj.org/article/74f14d0b65de4373a4a711df4e93d49c
Autor:
Javier eRiancho, Maria eRuiz-Soto, Nuria T Villagra, Jose eBerciano, Maria T Berciano, Miguel eLafarga
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 8 (2014)
We investigated neuronal self-defense mechanisms in a murine model of amyotrophic lateral sclerosis (ALS), the transgenic hSOD1G93A, during both the asymptomatic and symptomatic stages. This is an experimental model of endoplasmic reticulum (ER) stre
Externí odkaz:
https://doaj.org/article/6076f0980ace43dfa94c7dd07722fde0
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e17169 (2011)
BACKGROUND: Thyrotroph embryonic factor (TEF), a member of the PAR bZIP family of transcriptional regulators, has been involved in neurotransmitter homeostasis, amino acid metabolism, and regulation of apoptotic proteins. In spite of its relevance, n
Externí odkaz:
https://doaj.org/article/d783498ff9c74786afa82b0f09ab5ffd
Autor:
João Paulo Tavanez, Rocio Bengoechea, Maria T Berciano, Miguel Lafarga, Maria Carmo-Fonseca, Francisco J Enguita
Publikováno v:
PLoS ONE, Vol 4, Iss 7, p e6418 (2009)
Genomic instability at loci with tandem arrays of simple repeats is the cause for many neurological, neurodegenerative and neuromuscular diseases. When located in coding regions, disease-associated expansions of trinucleotide repeats are translated i
Externí odkaz:
https://doaj.org/article/e9596f8e4200445da3e8105d9a03841f