Zobrazeno 1 - 10
of 239
pro vyhledávání: '"Non-synonymous SNPs"'
Autor:
Fizzah Abid, Khushbukhat Khan, Yasmin Badshah, Naeem Mahmood Ashraf, Maria Shabbir, Arslan Hamid, Tayyaba Afsar, Ali Almajwal, Suhail Razak
Publikováno v:
Cancer Cell International, Vol 23, Iss 1, Pp 1-24 (2023)
Abstract Background PRKCG encodes PKC γ, which is categorized under the classical protein kinase C family. No studies have specifically established the relationship between PRKCG nsSNPs with structural and functional variations in PKC γ in the cont
Externí odkaz:
https://doaj.org/article/eca0b66a0ed24e0aac0fd4ff7b6278e2
Autor:
Sapna Pandey, Neha Maurya, Himanshu Avashthi, Pramod Katara, Satendra Singh, Budhayash Gautam, Dev Bukhsh Singh
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100817- (2023)
Parkinson’s disease (PD) is associated with a mutation in the PRKN (Parkin RBR E3 Ubiquitin Protein Ligase). PRKN functions as maintaining dopamine (DA) neuronal homeostasis and homeostasis dysfunction, which play an important role in early PD onse
Externí odkaz:
https://doaj.org/article/2eb2b74f5387403db4f4bc3ca22f6f97
Publikováno v:
Molecules, Vol 28, Iss 12, p 4648 (2023)
Angiopoietin-like proteins (ANGPTL) constitute a family of eight proteins (1–8) which play a pivotal role in the regulation of various pathophysiological processes. The current study sought to identify high-risk, “non-synonymous, single-nucleotid
Externí odkaz:
https://doaj.org/article/2521e2aa37b847d69cc407065b97b84d
Autor:
Mohammed Al-Shuhaib
Publikováno v:
BioTechnologia, Vol 100, Iss 4, Pp 429-439 (2019)
Leptin is a versatile hormone involved in many biological functions, including controlling body weight, energy homeostasis, reproduction, and immune function. Though exhaustive studies were performed on the bovine LEP gene, no efforts have been made
Externí odkaz:
https://doaj.org/article/291e7149f0024f37ac1077a93e72c306
Autor:
Yasir Ali, Faisal Ahmad, Muhammad Farhat Ullah, Noor Ul Haq, M. Inam Ul Haq, Abdul Aziz, Ferjeni Zouidi, M. Ijaz Khan, Sayed M. Eldin
Publikováno v:
Bioengineering, Vol 9, Iss 12, p 749 (2022)
Postaxial Polydactyly (PAP) is a congenital disorder of limb abnormalities characterized by posterior extra digits. Mutations in the N-terminal region of the Zinc finger protein 141 (ZNF141) gene were recently linked with PAP type A. Zinc finger prot
Externí odkaz:
https://doaj.org/article/a5ef5605b23e4e3496d73c3d83f78899
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-16 (2018)
Abstract Background Environmental stress induced genetic polymorphisms have been suggested to arbitrate functional modifications influencing adaptations in microbes. The relationship between the genetic processes and concomitant functional adaptation
Externí odkaz:
https://doaj.org/article/ac5ac79086fe49989707ffffc1c39c22
Autor:
Dipankor Chatterjee, Umar Faruq Chowdhury, Mohammad Umer Sharif Shohan, Md Mohasin, Yearul Kabir
Publikováno v:
Informatics in Medicine Unlocked, Vol 26, Iss , Pp 100728- (2021)
Ephrin type-A receptor 3 (EPHA3) is a receptor tyrosine kinase involved in many biological functions, including migration, adhesion, and so on. Dysregulation of the EPHA3 receptor gene can lead to various oncogenic events, such as prostate cancer and
Externí odkaz:
https://doaj.org/article/d6ec5a738c9646a29e8f6e7f3c919c4d
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