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Results 493 to 512 of 737
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TypeTitleAuthor(s)YearViews
Nef interaction with actin compromises human podocyte actin cytoskeletal integrityTan, R; Patni, H; Tandon, P; Luan, L; Sharma, B; Salhan, D; Saleem, MA; Mathieson, PW; Malhotra, A; Husain, M; Upadhya, P; Singhal, PC201314
 
Nephrin deficiency activates NF-κB and promotes glomerular injuryHussain, S; Romio, L; Saleem, M; Mathieson, P; Serrano, M; Moscat, J; Diaz-Meco, M; Scambler, P; Koziell, A200917
 
Nephrin is critical for the action of insulin on human glomerular podocytesCoward, RJM; Welsh, GI; Koziell, A; Hussain, S; Lennon, R; Ni, L; Tavaré, JM; Mathieson, PW; Saleem, MA20079
 
Nephrin sends us signalsMathieson, PW20034
 
Nephron-Experimental Nephrology: IntroductionMathieson, PW; Miner, JH20076
 
Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, podocin, and CD2 associated protein in cultured human podocytesCoward, RJM; Foster, RR; Patton, D; Ni, L; Lennon, R; Bates, DO; Harper, SJ; Mathieson, PW; Saleem, MA20058
 
Neurological deficits complicating thoracolumbar spinal pseudoarthrosis in ankylosing spondylitis: A report of four casesHo, EKW; Chan, FL; Upadhyay, SS; Chow, SP199254
 
New restriction fragment length polymorphism (probe E9) reveals the highest linkage disequilibrium in Italian CF patients.Devoto, M; De Benedetti, L; Ronchetto, P; Romano, L; Romeo, G; Tsui, LC; Dean, M; Collins, F; Seia, M; Piceni Sereni, L199082
 
Nicorandil as a novel therapy for advanced diabetic nephropathy in the eNOS-deficient mouseTanabe, K; Lanaspa, MA; Kitagawa, W; Rivard, CJ; Miyazaki, M; Klawitter, J; Schreiner, GF; Saleem, MA; Mathieson, PW; Makino, H; Johnson, RJ; Nakagawa, T201213
 
Nitric oxide contributes to tissue injury in mercuric chloride-induced autoimmunityWoolfson, RG; Qasim, FJ; Thiru, S; Oliveira, DBG; Neild, GH; Mathieson, PW19958
 
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 FamiliesBarr, CL; Wigg, KG; Zovko, E; Sandor, P; Tsui, LC1996186
 
No evidence for genetic heterogeneity in cystic fibrosis.Tsui, LC; Buchwald, M198874
 
Nonsteroidal anti-inflammatory drugs upregulate function of wild-type and mutant CFTRLi, J; Xiang, YY; Ye, L; Tsui, LC; MacDonald, JF; Hu, J; Lu, WY2008139
 
Northland ophiolite, New Zealand, and implications for plate- tectonic evolution of the southwest PacificMalpas, J; Sporli, KB; Black, PM; Smith, IEM199279
 
Novel conditionally immortalized human proximal tubule cell line expressing functional influx and efflux transportersWilmer, MJ; Saleem, MA; Masereeuw, R; Ni, L; Van Der Velden, TJ; Russel, FG; Mathieson, PW; Monnens, LA; Van Den Heuvel, LP; Levtchenko, EN20107
 
Novel cystic fibrosis mutation (2215insG) two adolescent Taiwanese siblingsWu, CL; Shu, SG; Zielenski, J; Chiang, CD; Tsui, LC2000241
 
A novel homozygous recessive mutation in the galactosyltransferase-I (B4GALT7) gene in individuals resembling the progeroid type of Ehlers-Danlos syndromeUl haque, MF; Teebi, AS; Al-ali, M; Al-mureikhi, MS; Kennedy, S; Al-thani, G; Zaidi, SHE; Tsui, L-C2003273
 
A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1Rafiq, MA; FaiyazulHaque, M; Ud Din, MA; Malik, S; Sohail, M; Anwar, M; Haque, S; Paterson, AD; Tsui, LC; Ahmad, W20051,660
 
A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndromeFaiyazUlHaque, M; Zaidi, SHE; AlSanna, N; Alswaid, A; Momenah, T; Kaya, N; AlDayel, F; Bouhoaigah, I; Saliem, M; Tsui, LC; Teebi, AS2009390
 
A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid typeFaiyazUlHaque, M; Zaidi, SHE; AlAli, M; AlMureikhi, MS; Kennedy, S; AlThani, G; Tsui, LC; Teebi, AS2004683
 
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