Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hamad S. Al-Otaibi"'
Autor:
Bodruzzaman Khan, Subhabrata Das, Nafis Shahid Fahim, Santanu Banerjee, Salma Khan, Mohammad Khalid Al-Sadoon, Hamad S. Al-Otaibi, Abu Reza Md. Towfiqul Islam
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-30 (2024)
Abstract Manual identification of tomato leaf diseases is a time-consuming and laborious process that may lead to inaccurate results without professional assistance. Therefore, an automated, early, and precise leaf disease recognition system is essen
Externí odkaz:
https://doaj.org/article/fc7db610572c44389f775cf17f7fd0c7
Autor:
Irfan Ahmad, Komal Mazhar, Muhammad Atiq, Amna Kahtan Khalaf, Muhammad Haroon U. Rashid, Muhammad Asif, Salman Ahmed, Zoha Adil, Amna Fayyaz, Mohammad Khalid Al-Sadoon, Hamad S. Al-Otaibi
Publikováno v:
PeerJ, Vol 12, p e17022 (2024)
Eucalyptus camaldulensis is a multifunctional tree and is globally used for the reclamation of problematic lands. Eucalyptus camaldulensis is prone to attack by a number of pathogens, but the most important threat is the Fusarium wilt (Fusarium oxysp
Externí odkaz:
https://doaj.org/article/79230d73b92543da8290c5aa8bc52051
Publikováno v:
Saudi Journal of Biological Sciences, Vol 24, Iss 4, Pp 925-928 (2017)
Turaif area located in the Northern border region of Saudi Arabia is one of the most important regions of the Kingdom. This work was proposed to throw light on the diversity of lizard fauna investigated through the collection and subsequent identific
Publikováno v:
Saudi Journal of Biological Sciences, Vol 23, Iss 5, Pp 642-648 (2016)
Turaif area located in the Northern border region of Saudi Arabia is one of the most important regions of the Kingdom. This work was proposed to throw light on the diversity of lizard fauna investigated through the collection and subsequent identific
Autor:
Omhani Malibari, Muhammad Saud, Hamad S. Al-Otaibi, Mohammad I. Samman, Essa Alharby, Sulman Basit, Ghadeer Alharbi
Publikováno v:
International Journal of Genetics and Molecular Biology. 8:11-17
The gene HMGCL encodes 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) lyase. Mutations in HMG-CoA lyase cause HMG-CoA lyase deficiency (HMGCLD), which is an autosomal recessive congenital disorder of metabolism. This study was designed to detect mutation i