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Results 494 to 513 of 738
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Nef interaction with actin compromises human podocyte actin cytoskeletal integrity
Experimental and Molecular Pathology
Tan, R; Patni, H; Tandon, P; Luan, L; Sharma, B; Salhan, D; Saleem, MA; Mathieson, PW; Malhotra, A; Husain, M; Upadhya, P; Singhal, PC201383
Nephrin deficiency activates NF-κB and promotes glomerular injury
Journal of the American Society of Nephrology
Hussain, S; Romio, L; Saleem, M; Mathieson, P; Serrano, M; Moscat, J; Diaz-Meco, M; Scambler, P; Koziell, A200965
Nephrin is critical for the action of insulin on human glomerular podocytes
Coward, RJM; Welsh, GI; Koziell, A; Hussain, S; Lennon, R; Ni, L; Tavaré, JM; Mathieson, PW; Saleem, MA200765
Nephrin sends us signals
Kidney International
Mathieson, PW200340
Nephron-Experimental Nephrology: Introduction
Nephron - Experimental Nephrology
Mathieson, PW; Miner, JH200734
Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, podocin, and CD2 associated protein in cultured human podocytes
Journal of the American Society of Nephrology
Coward, RJM; Foster, RR; Patton, D; Ni, L; Lennon, R; Bates, DO; Harper, SJ; Mathieson, PW; Saleem, MA200558
Neurological deficits complicating thoracolumbar spinal pseudoarthrosis in ankylosing spondylitis: A report of four cases
Journal of the Western Pacific Orthopaedic Association
Ho, EKW; Chan, FL; Upadhyay, SS; Chow, SP1992101
New restriction fragment length polymorphism (probe E9) reveals the highest linkage disequilibrium in Italian CF patients.
Acta Universitatis Carolinae Medica
Charles University in Prague, 1st Faculty of Medicine
Devoto, M; De Benedetti, L; Ronchetto, P; Romano, L; Romeo, G; Tsui, LC; Dean, M; Collins, F; Seia, M; Piceni Sereni, L1990165
Nicorandil as a novel therapy for advanced diabetic nephropathy in the eNOS-deficient mouse
American Journal of Physiology - Renal Physiology
Tanabe, K; Lanaspa, MA; Kitagawa, W; Rivard, CJ; Miyazaki, M; Klawitter, J; Schreiner, GF; Saleem, MA; Mathieson, PW; Makino, H; Johnson, RJ; Nakagawa, T201287
Nitric oxide contributes to tissue injury in mercuric chloride-induced autoimmunity
Biochemical and Biophysical Research Communications
Woolfson, RG; Qasim, FJ; Thiru, S; Oliveira, DBG; Neild, GH; Mathieson, PW199557
No Evidence for a Major Gene Effect of the Dopamine D4 Receptor Gene in the Susceptibility to Gilles de la Tourette Syndrome in Five Canadian Families
American Journal of Medical Genetics - Seminars in Medical Genetics
John Wiley & Sons, Inc.
Barr, CL; Wigg, KG; Zovko, E; Sandor, P; Tsui, LC1996246
No evidence for genetic heterogeneity in cystic fibrosis.
American Journal of Human Genetics
Cell Press. The Journal's web site is located at
Tsui, LC; Buchwald, M1988132
Nonsteroidal anti-inflammatory drugs upregulate function of wild-type and mutant CFTR
European Respiratory Journal
European Respiratory Society. The Journal's web site is located at
Li, J; Xiang, YY; Ye, L; Tsui, LC; MacDonald, JF; Hu, J; Lu, WY2008255
Northland ophiolite, New Zealand, and implications for plate- tectonic evolution of the southwest Pacific
Geological Society of America. The Journal's web site is located at
Malpas, J; Sporli, KB; Black, PM; Smith, IEM1992170
Novel conditionally immortalized human proximal tubule cell line expressing functional influx and efflux transporters
Cell and Tissue Research
Wilmer, MJ; Saleem, MA; Masereeuw, R; Ni, L; Van Der Velden, TJ; Russel, FG; Mathieson, PW; Monnens, LA; Van Den Heuvel, LP; Levtchenko, EN201058
Novel cystic fibrosis mutation (2215insG) two adolescent Taiwanese siblings
Journal of the Formosan Medical Association
Scientific Communications International Ltd. The Journal's web site is located at
Wu, CL; Shu, SG; Zielenski, J; Chiang, CD; Tsui, LC2000294
A novel homozygous recessive mutation in the galactosyltransferase-I (B4GALT7) gene in individuals resembling the progeroid type of Ehlers-Danlos syndrome
University of Chicago Press. The Journal's web site is located at
Ul haque, MF; Teebi, AS; Al-ali, M; Al-mureikhi, MS; Kennedy, S; Al-thani, G; Zaidi, SHE; Tsui, L-C2003359
A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1
Journal of Investigative Dermatology
Nature Publishing Group. The Journal's web site is located at
Rafiq, MA; FaiyazulHaque, M; Ud Din, MA; Malik, S; Sohail, M; Anwar, M; Haque, S; Paterson, AD; Tsui, LC; Ahmad, W20051,772
A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome
Elsevier Ireland Ltd. The Journal's web site is located at
FaiyazUlHaque, M; Zaidi, SHE; AlSanna, N; Alswaid, A; Momenah, T; Kaya, N; AlDayel, F; Bouhoaigah, I; Saliem, M; Tsui, LC; Teebi, AS2009517
A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type
American Journal of Medical Genetics
John Wiley & Sons, Inc. The Journal's web site is located at
FaiyazUlHaque, M; Zaidi, SHE; AlAli, M; AlMureikhi, MS; Kennedy, S; AlThani, G; Tsui, LC; Teebi, AS2004785
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