Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Carmen, Montano"'
Publikováno v:
SSRN Electronic Journal.
Autor:
Christian S. Thudium, Ansgar Schulz, Henrik Löfvall, Carmen Montano, Zsuzsanna Kertész, Kim Henriksen, Mehtap Sirin, Michael Rothe, Axel Schambach, Ilana Moscatelli, Johan Richter
Publikováno v:
Human gene therapy. 29(8)
Infantile malignant osteopetrosis (IMO) is a rare, lethal, autosomal recessive disorder characterized by nonfunctional osteoclasts. More than 50% of the patients have mutations in the TCIRG1 gene, encoding for a subunit of the osteoclast proton pump.
Akademický článek
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Autor:
Kim Henriksen, Johan Richter, Carmen Montano, Christian S. Thudium, Ansgar Schulz, Zsuzsanna Kertész, Henrik Löfvall, Ilana Moscatelli, Morten A. Karsdal, Carmen Flores Bjurström
Publikováno v:
Calcified tissue international. 99(6)
Infantile malignant osteopetrosis (IMO) is a rare, recessive disorder characterized by increased bone mass caused by dysfunctional osteoclasts. The disease is most often caused by mutations in the TCIRG1 gene encoding a subunit of the V-ATPase involv
Autor:
Kim Henriksen, Johan Richter, Carmen Montano, Ilana Moscatelli, Ansgar Schulz, Christian S. Thudium, Henrik Löfvall
Publikováno v:
Bone Abstracts.
Autor:
María Jesús Ramos, Magdalena Rudzińska, Elżbieta Radziejewska-Kubzdela, Anna Grygier, Maria Carmen Montano, Paweł Górnaś
Publikováno v:
European Journal of Lipid Science and Technology. 120:1700147
Kernels recovered from fruit pits of fourteen apricot (Prunus armeniaca L.) genotypes were tested for future application as feedstock for biodiesel production. The difference between the lowest and the highest oil yield between studied samples was ov
Autor:
J B, Demoulin, Sandrine, Medves, Federica, Toffalini, Ahmed, Essaghir, Anders, Kallin, Carmen, Montano, Amélie, Velghe, François, Duhoux
Publikováno v:
Bulletin et memoires de l'Academie royale de medecine de Belgique. 165(5-6)
Growth factors of the PDGF and FGF families act through receptor tyrosine kinases. These receptors can be activated by chromosomal rearrangements in myeloid neoplasms associated with hypereosinophilia. We identified a new fusion gene between KANK1 an