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Results 219 to 238 of 739
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TypeTitleAuthor(s)YearViews
Familial focal segmental glomerulosclerosis (FSGS)-linked α-actinin 4 (ACTN4) protein mutants lose ability to activate transcription by nuclear hormone receptors
Journal:
Journal of Biological Chemistry
Khurana, S; Chakraborty, S; Lam, M; Liu, Y; Su, Y-T; Zhao, X; Saleem, MA; Mathieson, PW; Bruggeman, LA; Kao, H-Y201265
 
Familial mesangio-capillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome
Journal:
Nephrology Dialysis Transplantation
Cooper, M; McGraw, ME; Unsworth, DJ; Mathieson, P200444
 
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13
Journal:
Clinical Genetics
Publisher:
Blackwell Munksgaard. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CGE
Zaidi, SHE; Peltekova, V; Meyer, S; Lindinger, A; Paterson, AD; Tsui, LC; FaiyazUlHaque, M; Teebi, AS2005656
 
Fat cell loss and mesangiocapillary glomerulonephritis: Chicken, egg or both?
Journal:
Nephron - Clinical Practice
Mathieson, PW; Keith Peters, D200428
 
Fat embolism in Hong Kong Chinese
Journal:
Journal of Bone and Joint Surgery - Series A
Publisher:
Journal of Bone and Joint Surgery. The Journal's web site is located at http://www.jbjs.org
Chow, SP; Hoaglund, FT198073
 
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1
Publisher:
University of Chicago Press. The Journal's web site is located at http://www.journals.uchicago.edu/AJHG
Scherer, SW; Poorkaj, P; Allen, T; Kim, J; Geshuri, D; Nunes, M; Soder, S; Stephens, K; Pagon, RA; Patton, MA; Berg, MA; Donlon, T; Rivera, H; Pfeiffer, RA; Naritomi, K; Hughes, H; Genuardi, M; Gurrieri, F; Neri, G; Lovrein, E; Magenis, E; Tsui, L-C; Evans, JP1994387
 
Fine mapping of the human and mouse genes for the type i procollagen COOH-terminal proteinase enhancer protein
Journal:
Genomics
Publisher:
Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ygeno
Takahara, K; Osborne, L; Elliott, RW; Tsui, LC; Scherer, SW; Greenspan, DS1996298
 
Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes
Journal:
Clinical Genetics
Publisher:
Blackwell Munksgaard. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CGE
FaiyazUlHaque, M; Zaidi, SHE; King, LM; Haque, S; Patel, M; Ahmad, M; Siddique, T; Ahmad, W; Tsui, LC; Cohn, DH2005996
 
First Joint Meeting of the French Society of Nephrology the UK Renal Association and the Nephrology Section of the Royal Society of Medicine. Royal Society of Medicine, London, February 28-29, 2008
Journal:
Nephron - Physiology
Mason, P; Mathieson, P; Ronco, P200826
 
FISH detection on DAPI-banded chromosomes.
Journal:
Methods in molecular biology (Clifton, N.J.)
Publisher:
Humana Press, Inc.
Heng, HH; Tsui, LC1994130
 
Flufenamic acid is a tool for investigating TRPC6-mediated calcium signalling in human conditionally immortalised podocytes and HEK293 cells
Journal:
Cell Calcium
Foster, RR; Zadeh, MAH; Welsh, GI; Satchell, SC; Ye, Y; Mathieson, PW; Bates, DO; Saleem, MA200974
 
Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3
Journal:
Cytogenetics and Cell Genetics
Publisher:
S Karger AG. The Journal's web site is located at http://www.karger.com/CGR
Heng, HHQ; Shi, XM; Tsui, LC1993291
 
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6
Journal:
Mammalian Genome
Publisher:
Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00335/
Crackower, MA; Heng, HHQ; Shi, X; Scherer, SW; Tsui, LC1997136
 
Fracture of the tibial tubercle in the adolescent
Journal:
Journal of Bone and Joint Surgery - Series B
Publisher:
British Editorial Society of Bone and Joint Surgery. The Journal's web site is located at http://www.jbjs.org.uk/
Chow, SP; Lam, JJ; Leong, JCY199075
 
Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia
Journal:
American Journal of Medical Genetics
Publisher:
John Wiley & Sons, Inc.
FaiyazUlHaque, M; Ahmad, W; Wahab, A; Haque, S; Azim, AC; Zaidi, SHE; Teebi, AS; Ahmad, M; Cohn, DH; Siddique, T; Tsui, LC2002360
 
A frameshift mutation in the γE-crystallin gene of the Elo mouse
Journal:
Nature Genetics
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com
Cartier, M; Breitman, ML; Tsui, LC1992251
 
Free chromatin mapping by FISH.
Journal:
Methods in molecular biology (Clifton, N.J.)
Publisher:
Humana Press, Inc.
Heng, HH; Tsui, LC1994109
 
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency
Journal:
Journal of Human Genetics
Publisher:
Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/10038/index.htm
Lu, YB; Kobayashi, K; Ushikai, M; Tabata, A; Iijima, M; Li, MX; Lei, L; Kawabe, K; Taura, S; Yang, Y; Liu, TT; Chiang, SH; Hsiao, KJ; Lau, YL; Tsui, LC; Lee, DH; Saheki, T2005939
 
From "Brain Drain" to "Brain Circulation" - rethinking the global knowledge economy: perspective from Hong KongTam, Paul KH2009204
 
Functional distinctions in cytosolic calcium regulation between cells of the glomerular filtration barrier
Journal:
Cell Calcium
Foster, RR; Welsh, GI; Satchell, SC; Marlow, RD; Wherlock, MD; Pons, D; Mathieson, PW; Bates, DO; Saleem, MA201057
 
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