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Katalin Csiszar Ph.D.
Affiliation:
University of Hawaii
Department of Complementary and Alternative Medicine
"Neurological Disorders and Mental Health"
Title: Professor
Address:
1960 East West Road Biomed 415
Honolulu, HI 96822
Contact:
Email: [email protected]
Telephone: 808-9569452
Publications
1.
Segond N, Degrelle SA, Berndt S, Clouqueur E, Rouault C, Saubamea B, Dessen P, PubMed
Fong KS, Csiszar K, Badet J, Evain-Brion D, Fournier T. Transcriptome Analysis of
PPAR? Target Genes Reveals the Involvement of Lysyl Oxidase in Human Placental
Cytotrophoblast Invasion. PLoS One. 2013; 8(11):e79413.
2.
Remus EW, O'Donnell RE, Rafferty K, Weiss D, Joseph G, Csiszar K, Fong SF, Taylor PubMed
WR. The role of lysyl oxidase family members in the stabilization of abdominal aortic
aneurysms. Am J Physiol Heart Circ Physiol. 2012 Oct 15; 303(8):H1067-75.
3.
Kelemen-Valkony I, Kiss M, Csiha J, Kiss A, Bircher U, Szidonya J, Maróy P, Juhász G, PubMed
Komonyi O, Csiszár K, Mink M. Drosophila basement membrane collagen col4a1
mutations cause severe myopathy. Matrix Biol. 2012 Jan; 31(1):29-37.
4.
Li PA, Rasquinha I, He QP, Siesjö BK, Csiszár K, Boyd CD, MacManus JP. PubMed
Hyperglycemia enhances DNA fragmentation after transient cerebral ischemia. J
Cereb Blood Flow Metab. 2001 May; 21(5):568-76.
5.
Urbán Z, Peyrol S, Plauchu H, Zabot MT, Lebwohl M, Schilling K, Green M, Boyd CD, PubMed
Csiszár K. Elastin gene deletions in Williams syndrome patients result in altered
deposition of elastic fibers in skin and a subclinical dermal phenotype. Pediatr
Dermatol. 2000 Jan-Feb; 17(1):12-20.
6.
Garibay-Tupas JL, Csiszár K, Fox M, Povey S, Bryant-Greenwood GD. Analysis of the PubMed
5'-upstream regions of the human relaxin H1 and H2 genes and their chromosomal
localization on chromosome 9p24.1 by radiation hybrid and breakpoint mapping. J
Mol Endocrinol. 1999 Dec; 23(3):355-65.
7.
Urbán Z, Michels VV, Thibodeau SN, Donis-Keller H, Csiszár K, Boyd CD. PubMed
Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in
reduced expression of two aberrantly spliced transcripts. Hum Genet. 1999 Feb;
104(2):135-42.
8.
del Rio T, Urbán Z, Csiszár K, Boyd CD. A gene-dosage PCR method for the detection PubMed
of elastin gene deletions in patients with Williams syndrome. Clin Genet. 1998 Aug;
54(2):129-35.
9.
Szabó Z, Light E, Boyd CD, Csiszár K. The human lysyl oxidase-like gene maps PubMed
between STS markers D15S215 and GHLC.GCT7C09 on chromosome 15. Hum Genet.
1997 Dec; 101(2):198-200.
10. Urbán Z, Csiszár K, Fekete G, Boyd CD. A tetranucleotide repeat polymorphism PubMed
within the human elastin gene (ELNi1). Clin Genet. 1997 Feb; 51(2):133-4.
11. Urbán Z, Helms C, Fekete G, Csiszár K, Bonnet D, Munnich A, Donis-Keller H, Boyd PubMed
CD. 7q11.23 deletions in Williams syndrome arise as a consequence of unequal
meiotic crossover. Am J Hum Genet. 1996 Oct; 59(4):958-62.
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