Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Norhan B.B. Mohammed"'
Autor:
Tahia H. Saleem, Mohammed H. Hassan, Ahmed El-Abd Ahmed, Ayat A. Sayed, Nahed A. Mohamed, Khalid I. Elsayh, Abdallah M.A.A. El-Ebidi, Norhan B.B. Mohammed
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 3, Pp 249-255 (2017)
Background: Gaucher’s disease (GD) is an autosomal recessive genetic disorder that results from pathogenic mutations of GBA gene encoding the enzyme glucocerebrosidase (acid β-glucosidase). Of the approximately 300 mutations associated with GD, 4
Externí odkaz:
https://doaj.org/article/3e66f328bc664d28b65423cc66806522
Autor:
Norhan B.B. Mohammed, Aristotelis Antonopoulos, Anne Dell, Stuart M. Haslam, Charles J. Dimitroff
Publikováno v:
Advances in Cancer Research ISBN: 9780323991773
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::041d93c59f1d96d20a4eea99c64d7aff
https://doi.org/10.1016/bs.acr.2022.06.001
https://doi.org/10.1016/bs.acr.2022.06.001
Autor:
Asmi Chakraborty, Mariana Perez, Jordan D. Carroll, Aristotelis Antonopoulos, Anne Dell, Liettel Ortega, Norhan B.B. Mohammed, Michael Wells, Caleb Staudinger, Anthony Griswold, Kevin B. Chandler, Cristina Marrero, Ramon Jimenez, Yoshihiko Tani, James S. Wilmott, John F. Thompson, Wei Wang, Robert Sackstein, Richard A. Scolyer, George F. Murphy, Stuart M. Haslam, Charles J. Dimitroff
Publikováno v:
J Invest Dermatol
The prognosis for patients with metastatic melanoma (MM) involving distant organs is grim, and treatment resistance is potentiated by tumor-initiating cells (TICs) that thrive under hypoxia. MM cells, including TICs, express a unique glycome featurin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e4ad9d696e7b84ab5b3f950daf22943
https://doi.org/10.1016/j.jid.2022.07.033
https://doi.org/10.1016/j.jid.2022.07.033
Autor:
Tahia H. Saleem, Mohammed H. Hassan, Ayat A. Sayed, Khalid I Elsayh, Ahmed El-Abd Ahmed, Norhan B.B. Mohammed
Publikováno v:
International Journal of Biochemistry Research & Review. 15:1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3598caa94ea6c886d1d744b49d4b002e
https://doi.org/10.9734/ijbcrr/2016/30768
https://doi.org/10.9734/ijbcrr/2016/30768
Autor:
Mohammed H. Hassan, Norhan B.B. Mohammed, Tahia H. Saleem, Ayat A. Sayed, Khalid I Elsayh, Abdallah M. A.A. El-Ebidi, Nahed A. Mohamed, Ahmed El-Abd Ahmed
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 18, No 3 (2017); 249-255
Background : Gaucher’s disease (GD) is an autosomal recessive genetic disorder that results from pathogenic mutations of GBA gene encoding the enzyme glucocerebrosidase (acid b-glucosidase). Of the approximately 300 mutations associated with GD, 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2fce00b0ab254a958cb7af16e509255