Zobrazeno 1 - 10
of 304
pro vyhledávání: '"SCNA"'
Autor:
Anna S. Vetchinova, Marina R. Kapkaeva, Mikhail V. Ivanov, Kristina A. Kutukova, Natalia M. Mudzhiri, Lydia E. Frumkina, Anatoly V. Brydun, Vladimir S. Sukhorukov, Sergey N. Illarioshkin
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 10, Pp 8395-8411 (2023)
Parkinson’s disease (PD) is the second most common neurodegenerative disease. Some cases of PD may be caused by genetic factors, among which mutations in the LRRK2 and SNCA genes play an important role. To develop effective neuroprotective strategi
Externí odkaz:
https://doaj.org/article/92addc3dbffb49a99bb77514da92d9d0
Publikováno v:
Cancer Biology & Medicine, Vol 19, Iss 5, Pp 685-695 (2022)
Objective: Lung cancer is the most common cause of cancer-related deaths worldwide. Somatic copy number alterations (SCNAs) have been used to predict responses to therapies in many cancers, including lung cancer. However, little is known about whethe
Externí odkaz:
https://doaj.org/article/965d3ccebb704637bf40555c415e30a4
Autor:
Ting Yue, Jingjing Li, Manguang Liang, Jiaman Yang, Zhiwen Ou, Shuchen Wang, Wuhua Ma, Dehui Fan
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Gastric cancer (GC) is the second leading cause of cancer-related mortality and the fifth most common cancer worldwide. However, the underlying mechanisms of competitive endogenous RNAs (ceRNAs) in GC are unclear. This study aimed to cons
Externí odkaz:
https://doaj.org/article/875cf5e7fe36407295ec514c815058f3
Autor:
Junzhi Zhou, Xiaohe Ma, Lu Xu, Qian Liang, Jian Mao, Jiang Liu, Miao Wang, Jiao Yuan, Yu‐sheng Cong
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 12, Pp n/a-n/a (2021)
Externí odkaz:
https://doaj.org/article/70c0d307233242aa9bd81e0c184bd919
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Gregory J. Kimmel, Richard J. Beck, Xiaoqing Yu, Thomas Veith, Samuel Bakhoum, Philipp M. Altrock, Noemi Andor
Publikováno v:
PLoS Computational Biology
The phenotypic efficacy of somatic copy number alterations (SCNAs) stems from their incidence per base pair of the genome, which is orders of magnitudes greater than that of point mutations. One mitotic event stands out in its potential to significan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83fb8b52ed0c04a7a4170d0860c28894
https://hdl.handle.net/21.11116/0000-000C-A258-A21.11116/0000-000C-A25A-8
https://hdl.handle.net/21.11116/0000-000C-A258-A21.11116/0000-000C-A25A-8
Autor:
Slavica Trajkova, Eleonora Di Gregorio, Giovanni Battista Ferrero, Diana Carli, Lisa Pavinato, Geoffroy Delplancq, Paul Kuentz, Alfredo Brusco
Publikováno v:
Brain Sciences, Vol 10, Iss 11, p 788 (2020)
Potocki-Shaffer syndrome (PSS) is a rare non-recurrent contiguous gene deletion syndrome involving chromosome 11p11.2. Current literature implies a minimal region with haploinsufficiency of three genes, ALX4 (parietal foramina), EXT2 (multiple exosto
Externí odkaz:
https://doaj.org/article/201bad60a79a48afbfa42430bbd52181
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.
Autor:
Jonas Bergh, Theodoros Foukakis, Pablo Moreno-Ruiz, Johan Hartman, Balazs Acs, Michele Simonetti, Susanne Agartz, Ning Zhang, Luuk Harbers, Dimitrios Salgkamis, David L. Rimm, Yalai Bai, Nicola Crosetto, Alexios Matikas, Artur Mezheyeuski, Ioannis Zerdes, Ceren Boyaci
Publikováno v:
npj Breast Cancer, Vol 7, Iss 1, Pp 1-11 (2021)
NPJ Breast Cancer
NPJ Breast Cancer
Emerging data indicate that genomic alterations can shape immune cell composition in early breast cancer. However, there is a need for complementary imaging and sequencing methods for the quantitative assessment of combined somatic copy number altera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::571cc412a6251f6b3303b0e878186200
https://doaj.org/article/3346ad4f61b5411594a62c963ed56bb4
https://doaj.org/article/3346ad4f61b5411594a62c963ed56bb4