[HTML][HTML] Synthesis and pharmacological activities of pyrazole derivatives: A review
…, Y Ramli, J Taoufik, YN Mabkhot, FA Al-Aizari, M Ansar - Molecules, 2018 - mdpi.com
Pyrazole and its derivatives are considered a pharmacologically important active scaffold
that possesses almost all types of pharmacological activities. The presence of this nucleus in …
that possesses almost all types of pharmacological activities. The presence of this nucleus in …
Modeling strategies of 3D woven composites: A review
M Ansar, W Xinwei, Z Chouwei - Composite structures, 2011 - Elsevier
… The in-plane elastic moduli E x and E y increase with m, ie, the more the warp tows (in …
-the-thickness stiffness E z can be achieved by keeping the values of m and λ around 1. …
-the-thickness stiffness E z can be achieved by keeping the values of m and λ around 1. …
A review of photocatalytic characterization, and environmental cleaning, of metal oxide nanostructured materials
Industrial waste is the primary source of highly toxic organic pollutants and heavy metal
contaminants. Treatment of such effluence is necessary to mitigate environmental pollution to …
contaminants. Treatment of such effluence is necessary to mitigate environmental pollution to …
[HTML][HTML] Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways
Nephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are
autosomal-recessive ciliopathies presenting with cystic kidneys, retinal degeneration, and …
autosomal-recessive ciliopathies presenting with cystic kidneys, retinal degeneration, and …
WDR62 is associated with the spindle pole and is mutated in human microcephaly
Autosomal recessive primary microcephaly (MCPH) is a disorder of neurodevelopment
resulting in a small brain 1 , 2 . We identified WDR62 as the second most common cause of …
resulting in a small brain 1 , 2 . We identified WDR62 as the second most common cause of …
Alterations of the CIB2 calcium-and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48
Sensorineural hearing loss is genetically heterogeneous. Here, we report that mutations in
CIB2, which encodes a calcium- and integrin-binding protein, are associated with …
CIB2, which encodes a calcium- and integrin-binding protein, are associated with …
[PDF][PDF] Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability
Causes of autosomal-recessive intellectual disability (ID) have, until very recently, been
under researched because of the high degree of genetic heterogeneity. However, now that …
under researched because of the high degree of genetic heterogeneity. However, now that …
Land productivity and water use efficiency of maize-soybean strip intercropping systems in semi-arid areas: A case study in Punjab Province, Pakistan
…, H Gitari, S Ahmad, M Battaglia, M Ansar… - Journal of Cleaner …, 2021 - Elsevier
… from a 36 m 2 (6 m × 6 m) area for SM, SS, 2M2S, and a 43.2 m 2 (7.2 m × 6 m) area for 2M3S
… CW was also considered zero because the research site's water table was 65 m below the …
… CW was also considered zero because the research site's water table was 65 m below the …
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families
Approximately 1% of the global population is affected by intellectual disability (ID), and the
majority receive no molecular diagnosis. Previous studies have indicated high levels of …
majority receive no molecular diagnosis. Previous studies have indicated high levels of …
[HTML][HTML] Crop photosynthetic response to light quality and light intensity
Under natural conditions, plants constantly encounter various biotic and abiotic factors,
which can potentially restrict plant growth and development and even limit crop productivity. …
which can potentially restrict plant growth and development and even limit crop productivity. …