User profiles for "author:S N Mohammed"

Suhaila N. Mohammed

University of Baghdad-College of Science-Computer Science Department
Verified email at sc.uobaghdad.edu.iq
Cited by 170

[HTML][HTML] Congenital leptin deficiency is associated with severe early-onset obesity in humans

CT Montague, IS Farooqi, JP Whitehead, MA Soos… - Nature, 1997 - nature.com
The extreme obesity of the obese (ob/ob) mouse is attributable to mutations in the gene
encoding leptin, an adipocyte-specific secreted protein which has profound effects on …

A review of the role of carbon nanotubes for cancer treatment based on photothermal and photodynamic therapy techniques

MF Naief, SN Mohammed, HJ Mayouf… - Journal of …, 2023 - Elsevier
Carbon nanostructures have special optical characteristics that confer them with effective
light-to-heat conversion ability. They can also increase the local temperature by activating …

[HTML][HTML] How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

S Banka, R Veeramachaneni, W Reardon… - European Journal of …, 2012 - nature.com
MLL2 mutations are detected in 55 to 80% of patients with Kabuki syndrome (KS). In 20 to
45% patients with KS, the genetic basis remains unknown, suggesting possible genetic …

Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis

SRF Twigg, E Vorgia, SJ McGowan, I Peraki… - Nature …, 2013 - nature.com
The extracellular signal–related kinases 1 and 2 (ERK1/2) are key proteins mediating
mitogen-activated protein kinase signaling downstream of RAS: phosphorylation of ERK1/2 …

Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal …

J Kohlhase, L Schubert, M Liebers, A Rauch… - Journal of medical …, 2003 - jmg.bmj.com
We have recently shown that Okihiro syndrome results from mutation in the putative zinc
finger transcription factor gene SALL4 on chromosome 20q13. 13-13.2. There is …

Polymicrogyria and deletion 22q11. 2 syndrome: window to the etiology of a common cortical malformation

NH Robin, CJ Taylor… - American Journal of …, 2006 - Wiley Online Library
Several brain malformations have been described in rare patients with the deletion 22q11. 2
syndrome (DEL22q11) including agenesis of the corpus callosum, pachygyria or …

Growth of large-scale GaN nanowires and tubes by direct reaction of Ga with

M He, I Minus, P Zhou, SN Mohammed… - Applied Physics …, 2000 - pubs.aip.org
Large-scale wurtzite GaN nanowires and nanotubes were grown by direct reaction of metal
gallium vapor with flowing ammonia in an 850–900° C horizontal oven. The cylindrical …

“He will crush you like an academic ninja!”: Exploring teacher ratings on ratemyprofessors. com

J Kindred, SN Mohammed - Journal of Computer-Mediated …, 2005 - academic.oup.com
This study examines students' motives for use and perceptions of the web site http://www.
ratemyprofessors. com, one of the main sites that allow students to post anonymous ratings …

Effect of iron doped Zinc oxide nanoparticles coating in the anode on current generation in microbial electrochemical cells

H Muthukumar, SN Mohammed… - International Journal of …, 2019 - Elsevier
In this study, Iron doped Zinc oxide (Fesingle bondZnO) nanoparticles (NPs) were
synthesized and coated on carbon paper electrode. The NPs and NPs coated electrode …

Novel combination of multi-walled carbon nanotubes and gold nanocomposite for photothermal therapy in human breast cancer model

SN Mohammed, AM Mohammed, KF Al-Rawi - Steroids, 2022 - Elsevier
Despite current medical advancements, the resistance of malignant tumours to conventional
medical therapies highlights the need for innovative therapeutic techniques. Numerous …