Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Exostosin-2"'
Autor:
Serge Y. Ouedraogo, Daméhan Tchelougou, Jonas K. Kologo, Herman K. Sombie, Moutanou M.J. Zeye, Rebeca T. Compaore, Abdoul K. Ouattara, Abel P. Sorgho, Dorcas Obiri-Yeboah, Serge T. Soubeiga, Issoufou Nagabila, Albert T. Yonli, Florencia W. Djigma, Jacques Simpore
Publikováno v:
Journal of Public Health in Africa, Vol 11, Iss 1 (2020)
Recent genome-wide association studies and replication analyses have reported the association of variants of the exostosin- 2 gene (EXT2) and risk of type 2 diabetes (T2D) in some populations, but not in others. This study aimed to characterize the v
Externí odkaz:
https://doaj.org/article/adddfeceb3ee4ff48a6bedf75a11a965
Publikováno v:
The Journal of Biological Chemistry
Fibronectin (FN), an essential component of the extracellular matrix (ECM), is assembled via a cell-mediated process in which integrin receptors bind secreted FN and mediate its polymerization into fibrils that extend between cells, ultimately formin
Autor:
Issoufou Nagabila, Serge Yannick Ouedraogo, Abel Pegdwendé Sorgho, Jonas Koudougou Kologo, Florencia Wendkuuni Djigma, Herman Karim Sombie, Dorcas Obiri-Yeboah, Moutanou Modeste Judes Zeye, Daméhan Tchelougou, Serge Théophile Soubeiga, Albert Théophane Yonli, Jacques Simpore, Abdoul Karim Ouattara, Rebeca Tegwindé Compaore
Publikováno v:
Journal of Public Health in Africa, Vol 11, Iss 1 (2020)
Journal of Public Health in Africa
Journal of Public Health in Africa
Recent genome-wide association studies and replication analyses have reported the association of variants of the exostosin- 2 gene (EXT2) and risk of type 2 diabetes (T2D) in some populations, but not in others. This study aimed to characterize the v
Autor:
Antonio Novelli, Emanuele Bellacchio, Romina Ficarella, Maria Fatima Antonucci, Dario Cocciadiferro, Emanuela Ponzi, Mattia Gentile, Emanuele Agolini
Publikováno v:
Clinical Genetics. 95:165-171
Biallelic exostosin-2 (EXT2) pathogenic variants have been described as the cause of the Seizures-Scoliosis-Macrocephaly syndrome (OMIM 616682) characterized by intellectual disability, facial dysmorphisms and seizures. More recently, it has been pro
Publikováno v:
Oncology Letters
Hereditary multiple osteochondroma (HMO) is an autosomal dominant genetic disorder characterized by multiple outgrowing bony tumors capped by cartilage, generally affecting the metaphyses. The disease is known as hereditary multiple exostoses, famili
Autor:
A. Hari Reddi, Araceli Cuellar
Publikováno v:
International Orthopaedics. 37:1591-1596
Frequent benign outgrowths from bone known as osteochondromas, exhibiting typical endochondral ossification, are reported from single to multiple lesions. Characterised by a high incidence of osteochondromas and skeletal deformities, multiple heredit
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Development (Cambridge, England). 129(9)
Sonic hedgehog promotes proliferation of developing cerebellar granule cells. As sonic hedgehog is expressed in the cerebellum throughout life it is not clear why proliferation occurs only in the early postnatal period and only in the external granul
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.