Katalin Csiszar to Chromosome Mapping
This is a "connection" page, showing publications Katalin Csiszar has written about Chromosome Mapping.
Connection Strength
0.570
-
Jourdan-Le Saux C, Le Saux O, Gleyzal C, Sommer P, Csiszar K. The mouse lysyl oxidase-like 2 gene (mLOXL2) maps to chromosome 14 and is highly expressed in skin, lung and thymus. Matrix Biol. 2000 May; 19(2):179-83.
Score: 0.183
-
Jourdan-Le Saux C, Le Saux O, Donlon T, Boyd CD, Csiszar K. The human lysyl oxidase-related gene (LOXL2) maps between markers D8S280 and D8S278 on chromosome 8p21.2-p21.3. Genomics. 1998 Jul 15; 51(2):305-7.
Score: 0.162
-
Molnar J, Ujfaludi Z, Fong SF, Bollinger JA, Waro G, Fogelgren B, Dooley DM, Mink M, Csiszar K. Drosophila lysyl oxidases Dmloxl-1 and Dmloxl-2 are differentially expressed and the active DmLOXL-1 influences gene expression and development. J Biol Chem. 2005 Jun 17; 280(24):22977-85.
Score: 0.064
-
Csiszar K. Lysyl oxidases: a novel multifunctional amine oxidase family. Prog Nucleic Acid Res Mol Biol. 2001; 70:1-32.
Score: 0.048
-
Szab? Z, Light E, Boyd CD, Csisz?r K. The human lysyl oxidase-like gene maps between STS markers D15S215 and GHLC.GCT7C09 on chromosome 15. Hum Genet. 1997 Dec; 101(2):198-200.
Score: 0.039
-
Wydner KS, Kim Y, Csiszar K, Boyd CD, Passmore HC. An intron capture strategy used to identify and map a lysyl oxidase-like gene on chromosome 9 in the mouse. Genomics. 1997 Mar 01; 40(2):342-5.
Score: 0.037
-
Schmidt H, Semjonow A, Csiszar K, Korsching E, Brandt B, Eltze E. [Mapping of a deletion interval on 8p21-22 in prostate cancer by gene dosage PCR]. Verh Dtsch Ges Pathol. 2007; 91:302-7.
Score: 0.018
-
Le Saux O, Urban Z, G?ring HH, Csiszar K, Pope FM, Richards A, Pasquali-Ronchetti I, Terry S, Bercovitch L, Lebwohl MG, Breuning M, van den Berg P, Kornet L, Doggett N, Ott J, de Jong PT, Bergen AA, Boyd CD. Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16. Genomics. 1999 Nov 15; 62(1):1-10.
Score: 0.011
-
Urb?n Z, Helms C, Fekete G, Csisz?r K, Bonnet D, Munnich A, Donis-Keller H, Boyd 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.
Score: 0.009