User profiles for M. Ansar

Muhammad Ansar

- Verified email at qau.edu.pk - Cited by 4720

Muhammad Ansar

- Verified email at fa2.ch - Cited by 1103

[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 …

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. …

A review of photocatalytic characterization, and environmental cleaning, of metal oxide nanostructured materials

…, A Haider, S Naz, J Haider, A Raza, MT Ansar… - Sustainable Materials …, 2021 - Elsevier
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 …

[HTML][HTML] Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

…, HM Reutter, WS Lane, MA Rafiq, A Noor, M Ansar… - Cell, 2011 - cell.com
Nephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are
autosomal-recessive ciliopathies presenting with cystic kidneys, retinal degeneration, and …

WDR62 is associated with the spindle pole and is mutated in human microcephaly

…, JJ Cox, G Thornton, R Kausar, M Ansar… - Nature …, 2010 - nature.com
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 …

Alterations of the CIB2 calcium-and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

…, LV Parise, S Basit, A Wali, M Ayub, M Ansar… - Nature …, 2012 - nature.com
Sensorineural hearing loss is genetically heterogeneous. Here, we report that mutations in
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

…, C Windpassinger, S Ibrahim, M Frye, M Ansar… - The American Journal of …, 2012 - cell.com
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 …

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 …

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

…, P John, A Mir, M Ansar, L French, M Ayub… - Molecular …, 2018 - nature.com
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 …

[HTML][HTML] Crop photosynthetic response to light quality and light intensity

…, R Ali, Y Fan, M Mumtaz, M Shoaib, M Ansar… - Journal of Integrative …, 2021 - Elsevier
Under natural conditions, plants constantly encounter various biotic and abiotic factors,
which can potentially restrict plant growth and development and even limit crop productivity. …