Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Amira M. Embaby"'
Publikováno v:
AMB Express, Vol 13, Iss 1, Pp 1-16 (2023)
Abstract Despite the great potential of cold-adapted pullulanase type I in tremendous industrial applications, the majority of commercialized pullulnases type I are of mesophilic and thermophilic origin so far. Hence, the present study underlines clo
Externí odkaz:
https://doaj.org/article/256ae2d50c2443bdbb8512b4d6c30d1d
Autor:
Amira M. Embaby, Hoda E. Mahmoud
Publikováno v:
AMB Express, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Acetylxylan esterase plays a crucial role in xylan hydrolysis as the acetyl side-groups restrict endoxylanase action by stearic hindrance. In this study, an acetylxylan esterase (AXE-HAS10: 960 bp & 319 a.a) putative ORF from Halalkalibacter
Externí odkaz:
https://doaj.org/article/f51df690f5e54918abde111f3f138314
Autor:
Shaymaa W. El-Far, Heba Sh. Kassem, Amira M. Embaby, Abir A. Saad, Nader Mowafy, Medhat Haroun
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-7 (2022)
Abstract Background T2DM is a polygenic, metabolic complex and multifactorial disease. Several genes contribute to risk of type 2 diabetes and metabolic syndrome among different populations. Results An relationship between three identified CAPN-10 va
Externí odkaz:
https://doaj.org/article/4240631294594f8e9e8bc914354b84d7
Publikováno v:
FEBS Open Bio, Vol 11, Iss 9, Pp 2560-2575 (2021)
Cholesterol oxidases (CHOXs) are flavin‐adenine dinucleotide‐dependent oxidoreductases with a range of biotechnological applications. There remains an urgent need to identify novel CHOX family members to meet the demands of enzyme markets worldwi
Externí odkaz:
https://doaj.org/article/b897195d298249f48ec3c788bd781887
Publikováno v:
AMB Express, Vol 13, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/e56706c2df1c4dabb89d30d2164679de
Autor:
Huda Naeim, Amr El-Hawiet, Raoufa A. Abdel Rahman, Ahmed Hussein, Maha A. El Demellawy, Amira M. Embaby
Publikováno v:
BMC Complementary Medicine and Therapies, Vol 20, Iss 1, Pp 1-13 (2020)
Abstract Background In the context of searching for potent, safe, natural antimicrobial agents to combate the global antimicrobial resistance (AMR) phenomenon, the current study evaluates for the first time ever, the broad-spectrum antimicrobial acti
Externí odkaz:
https://doaj.org/article/d1516803235243bbadd58c3e1cd3978a
Autor:
Nehad Noby, Husam Sabah Auhim, Samuel Winter, Harley L. Worthy, Amira M. Embaby, Hesham Saeed, Ahmed Hussein, Christopher R. Pudney, Pierre J. Rizkallah, Stephen A. Wells, D. Dafydd Jones
Publikováno v:
Open Biology, Vol 11, Iss 12 (2021)
Here we determined the structure of a cold active family IV esterase (EstN7) cloned from Bacillus cohnii strain N1. EstN7 is a dimer with a classical α/β hydrolase fold. It has an acidic surface that is thought to play a role in cold-adaption by re
Externí odkaz:
https://doaj.org/article/742a9bfe43b248879d57a96a80adc331
Publikováno v:
Journal of Fungi, Vol 7, Iss 9, p 696 (2021)
The present work highlights the valorization of the bulky recalcitrant lignocellulose byproduct wheat straw (WS) for the enhanced production of value-added xylanase by the locally sourced novel Penicillium chrysogenum strain A3 DSM105774 for the firs
Externí odkaz:
https://doaj.org/article/d0a661d46fac42a585c18ecf3daac1de
Autor:
Ali Salim Al-shehmany Al-shehmany, Ahmad A. El- Kafoury El- Kafoury, Ahmad A. El- Kafoury * El- Kafoury, Amira M. Embaby Embaby
Publikováno v:
مجلة مركز بحوث التقنيات الاحيائية, Vol 9, Iss 2 (2015)
The human vitamin D receptor (VDR) gene is located on chromosome 12q12–q14, and four common nucleotide polymorphisms have been identified. Several studies have found a relationship between polymorphisms of the (VDR) gene and development of type 1 d
Externí odkaz:
https://doaj.org/article/82cbe419581a4f16b55ae1b11828e92a
Autor:
Ali Salim Al-shehmany Al-shehmany, Ahmad A. El- Kafoury El- Kafoury, Medhat A. Haroun Haroun, Amira M. Embaby Embaby
Publikováno v:
مجلة مركز بحوث التقنيات الاحيائية, Vol 9, Iss 2 (2015)
The protein tyrosine phosphatase, nonreceptor 22 gene (PTPN22) maps at human chromosome 1p13.3 which encodes an important negative regulator of T-cell activation, lymphoid-specific phosphatase (Lyp). The PTPN22 gene has been shown to associate with a
Externí odkaz:
https://doaj.org/article/ad45a7de9bf24e51a8cbc2244a076fcf