Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Oum Kaltoum Ait Boujmia"'
Publikováno v:
Asian Pacific Journal of Cancer Biology, Vol 6, Iss 1, Pp 5-13 (2021)
Acute myeloïd leukemia (AML) is the most frequent form of acute leukemia among adults and the most aggressive type of leukemia, which is associated with the lowest survival rate. Patients with AML are treated with intensive chemotherapy and many fac
Externí odkaz:
https://doaj.org/article/420d75f2d9af44afb60191008a025c4c
Autor:
Oum Kaltoum Ait Boujmia, Sellama Nadifi, Hind Dehbi, Yaya Kassogue, Mouna Lamchahab, Asma Quessar
Publikováno v:
Middle East Journal of Cancer, Vol 11, Iss 2, Pp 127-139 (2020)
Background: Acute myeloid leukemia (AML) is a complex disease that is linked to genetic and environmental factors. The gluthatione S-transferase (GST) is a family of enzymes that play a crucial role in the detoxification of carcinogens. These compoun
Externí odkaz:
https://doaj.org/article/5f94afa51b42499bb65ac85bc8b3bbee
Publikováno v:
IBRO Reports, Vol 5, Iss , Pp 133-136 (2018)
Glioblastoma is the most aggressive malignant type of central nervous system tumors. The literature review revealed that the most common genetic abnormalities in primary and secondary glioblastomas are IDH1 / 2 mutations, p53 mutations, and overexpre
Externí odkaz:
https://doaj.org/article/4e45c51b12774c83b4672ba3820596f5
Autor:
Hasna Hamdaoui, Oumaima Benlarroubia, Oum Kaltoum Ait Boujmia, Hossein Mossafa, Karim Ouldim, Aziza Belkhayat, Imane Smyej, Houda Benrahma, Hind Dehbi, Fatima Chegdani
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Abstract Background Multiple myeloma (MM) is a disease characterized by heterogeneous clinical presentations as well as complex genetic and molecular abnormalities. In MM, cytogenetic analysis is a challenge because of the low proliferation of malign
Externí odkaz:
https://doaj.org/article/1f5fda75ed0a41359efd3d2eac8a7bcd
Publikováno v:
European Journal of Ophthalmology. 31:2796-2807
Primary congenital glaucoma (PCG) is a rare and severe form of glaucoma and is usually transmitted as an autosomal-recessive disease. However, PCG is more common in certain ethnic and geographic groups where consanguineous relationships are common. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::218200f322d45532b9bfcb7cb98826f2
https://doi.org/10.1177/11206721211016308
https://doi.org/10.1177/11206721211016308
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
The human multidrug resistance MDR1 gene plays a crucial role in the absorption, transport, metabolism and elimination of harmful compounds. An impaired metabolism of these compounds related to genetic polymorphism may cause cancer such as acute myel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58ab393f7cf14458b7818bc2a176adc2
https://doi.org/10.31557/apjcp.2020.21.7.1899
https://doi.org/10.31557/apjcp.2020.21.7.1899
Publikováno v:
European journal of ophthalmology. 31(6)
Primary congenital glaucoma (PCG) is a rare and severe form of glaucoma and is usually transmitted as an autosomal-recessive disease. However, PCG is more common in certain ethnic and geographic groups where consanguineous relationships are common. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd41f70d37f0fc7238f3270f4170c025
https://pubmed.ncbi.nlm.nih.gov/34020567
https://pubmed.ncbi.nlm.nih.gov/34020567
Autor:
Oum Kaltoum Ait Boujmia
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 394(6)
V-domain Ig suppressor of T cell activation (VISTA) is a transmembrane protein that plays a crucial role in the regulation of antitumor immunity. Therapeutic intervention that inhibits the VISTA pathway constitutes a new approach in the treatment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3aa9fd5b974e5e1ab03d01a7b8679f5c
https://pubmed.ncbi.nlm.nih.gov/33616679
https://pubmed.ncbi.nlm.nih.gov/33616679
Autor:
Karim Ouldim, Hossein Mossafa, Hind Dehbi, Imane Smyej, Oum Kaltoum Ait Boujmia, Houda Benrahma, Oumaima Benlarroubia, Hasna Hamdaoui, Aziza Belkhayat, Fatima Chegdani
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Background Multiple myeloma (MM) is a disease characterized by heterogeneous clinical presentations as well as complex genetic and molecular abnormalities. In MM, cytogenetic analysis is a challenge because of the low proliferation of malignant plasm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb821305749e11a3640815547dea8b02
https://doi.org/10.1002/mgg3.1363
https://doi.org/10.1002/mgg3.1363
Publikováno v:
IBRO Reports
IBRO Reports, Vol 5, Iss, Pp 133-136 (2018)
IBRO Reports, Vol 5, Iss, Pp 133-136 (2018)
Glioblastoma is the most aggressive malignant type of central nervous system tumors. The literature review revealed that the most common genetic abnormalities in primary and secondary glioblastomas are IDH1 / 2 mutations, p53 mutations, and overexpre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cbcdb698865e837f0c630b5885685d
http://europepmc.org/articles/PMC6287047
http://europepmc.org/articles/PMC6287047