Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andrea Valls"'
Autor:
Anabel Rico, Andrea Valls, Garazi Guembelzu, Margarita Azpitarte, Ana Aiastui, Mónica Zufiria, Oihane Jaka, Adolfo López de Munain, Amets Sáenz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-16 (2023)
Abstract Background Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy due to mutations in the CAPN3 gene. While the pathophysiology of this disease has not been clearly established yet, Wnt and
Externí odkaz:
https://doaj.org/article/c98a543474c243b18fb6ae233988a467
Autor:
Anabel Rico, Garazi Guembelzu, Valle Palomo, Ana Martínez, Ana Aiastui, Leire Casas-Fraile, Andrea Valls, Adolfo López de Munain, Amets Sáenz
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 14, p 7367 (2021)
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while the pathophysiological mec
Externí odkaz:
https://doaj.org/article/f620c792fcf24c9dbeb406f528e23112
Autor:
Juan Fernando García, David Reguera, Andrea Valls, Anna Aviñó, Arnau Dominguez, Ramon Eritja, Raimundo Gargallo
In this work, the use of DNA-stabilized fluorescent silver nanoclusters for the detection of target pyrimidine-rich DNA sequences by formation of parallel and antiparallel triplex structures is studied by molecular fluorescence spectroscopy. In the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a7629f09479ec8f019fb9a22055c3bd
http://hdl.handle.net/10261/307827
http://hdl.handle.net/10261/307827
Autor:
Leire Casas-Fraile, Valle Palomo, Garazi Guembelzu, Anabel Rico, Ana Aiastui, Amets Sáenz, Adolfo López de Munain, Andrea Valls, Ana Martínez
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 14
International Journal of Molecular Sciences, Vol 22, Iss 7367, p 7367 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Volume 22
Issue 14
International Journal of Molecular Sciences, Vol 22, Iss 7367, p 7367 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
18 p.-8 fig.-1 tab.
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while t
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while t