Zobrazeno 1 - 10
of 174
pro vyhledávání: '"MLH1 GENE"'
Autor:
Saeied Malekzadeh, Sara Ghaffarian
Publikováno v:
Iranian South Medical Journal, Vol 26, Iss 3, Pp 155-166 (2024)
Background: The MisMatch Repair (MMR) system is a conserved system with a key role in genetic stability and replication integrity. The MLH1 gene is one of the four main components of the MMR complex. This study was conducted to assess the association
Externí odkaz:
https://doaj.org/article/efe4cc4cda9a4a569f11a48ff57a7a24
Publikováno v:
Journal of Advanced Pharmaceutical Technology & Research, Vol 15, Iss 1, Pp 43-48 (2024)
The major mortality factor for women globally is breast cancer, and current treatments have several adverse effects. Hesperetin (HSP) is a flavone that occurs naturally with anti-tumor capabilities and has been investigated as a potential treatment f
Externí odkaz:
https://doaj.org/article/82d969b1cfd848b29869a1d13c399814
Publikováno v:
Acta Crystallographica: Section F, Structural Biology Communications. Aug2015, Vol. 71 Issue 8, p981-985. 5p.
Autor:
Muhsin Jamil Abdulwahid, Mustafa Saber Al-Attar, Samiaa J. Abdulwahid-Kurdi, Karzan Abdulmuhsin Mohammad
Publikováno v:
Zanco Journal of Pure and Applied Sciences, Vol 35, Iss 6 (2023)
To ensure the accuracy of DNA replication, to maintain genome stability, and to assure the preservation of a species, the DNA in the cell should be constantly repaired. The mismatch repair (MMR) process is crucial for gametogenesis, meiotic recombina
Externí odkaz:
https://doaj.org/article/b87292f994174da88bd8f4e5b411ae6a
Publikováno v:
Journal of Advanced Pharmaceutical Technology & Research, Vol 14, Iss 4, Pp 338-344 (2023)
Hesperetin (HSP), a flavonoid, has been validated to modify gene expression and function as an epigenetic agent to stop the development of breast carcinoma cells. HSP was investigated in this research to evaluate the expression of the MLH1 and MSH2 g
Externí odkaz:
https://doaj.org/article/0f24c29ed2584f35a87665ace5b86c1b
Autor:
Yasuyuki Miyakura1,2 miyakura@jichi.ac.jp, Makiko Tahara1,2 magikuri26@yahoo.co.jp, Lefor, Alan T.1 alefor@jichi.ac.jp, Yoshikazu Yasuda1 yyasuda@jichi.ac.jp, Kokichi Sugano2 ksugano@tcc.pref.tochigi.lg.jp
Publikováno v:
BMC Research Notes. 2014, Vol. 7 Issue 1, p1-21. 21p. 1 Diagram, 4 Charts, 1 Graph.
Autor:
Marqués-Lespier, Juan M.1,2, Diaz-Algorri, Yaritza2, Gonzalez-Pons, Maria2, Cruz-Correa, Marcia2,3 marcia.cruz1@upr.edu
Publikováno v:
Gastroenterology Research & Practice. 2014, p1-7. 7p.
Autor:
Firas Akrout, Ahlem Achour, Carli M. J. Tops, Richard Gallon, Rym Meddeb, Sameh Achoura, Mariem Ben Rekaya, Emna Hamdeni, Soumaya Rammeh, Ridha Chkili, Nada Mansouri, Neila Belguith, Ridha Mrad
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder caused by biallelic germline mutations in one of the mismatch repair genes. Carriers are at exceptionally high risk for developing, typically in
Externí odkaz:
https://doaj.org/article/5c319bf8d8d8419f96e3348ff672efc1
Autor:
Petersen, Sanne M.1 tvoh@rh.dk, Dandanell, Mette1, Rasmussen, Lene J.2, Gerdes, Anne-Marie3, Krogh, Lotte N.4, Bernstein, Inge5, Okkels, Henrik6, Wikman, Friedrik7, Nielsen, Finn C.1, Hansen, Thomas v. O.1
Publikováno v:
BMC Medical Genetics. 2013, Vol. 14 Issue 1, p1-7. 7p.
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