Kanters JK - Search Results

1

First-Trimester Maternal Serum Adiponectin/Leptin Ratio in Pre-Eclampsia and Fetal Growth.

de Knegt VE, Hedley PL, Eltvedt AK, Placing S, Wøjdemann K, Shalmi AC, Rode L, Kanters JK, Sundberg K, Tabor A, Lausten-Thomsen U, Christiansen M. de Knegt VE, et al. Among authors: kanters jk. Life (Basel). 2023 Jan 3;13(1):130. doi: 10.3390/life13010130. Life (Basel). 2023. PMID: 36676079 Free PMC article.

2

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome.

Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M. Larsen LA, et al. Among authors: kanters jk. Clin Chim Acta. 1999 Feb;280(1-2):113-25. doi: 10.1016/s0009-8981(98)00177-6. Clin Chim Acta. 1999. PMID: 10090529

3

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M. Larsen LA, et al. Among authors: kanters jk. Eur J Hum Genet. 1999 Sep;7(6):724-8. doi: 10.1038/sj.ejhg.5200323. Eur J Hum Genet. 1999. PMID: 10482963

4

Does KCNE5 play a role in long QT syndrome?

Hofman-Bang J, Jespersen T, Grunnet M, Larsen LA, Andersen PS, Kanters JK, Kjeldsen K, Christiansen M. Hofman-Bang J, et al. Among authors: kanters jk. Clin Chim Acta. 2004 Jul;345(1-2):49-53. doi: 10.1016/j.cccn.2004.02.033. Clin Chim Acta. 2004. PMID: 15193977

5

Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.

Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K. Christiansen M, et al. Among authors: kanters jk. Am J Cardiol. 2005 Feb 1;95(3):433-4. doi: 10.1016/j.amjcard.2004.09.054. Am J Cardiol. 2005. PMID: 15670565

6

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.

Hofman-Bang J, Behr ER, Hedley P, Tfelt-Hansen J, Kanters JK, Haunsøe S, McKenna WJ, Christiansen M. Hofman-Bang J, et al. Among authors: kanters jk. Clin Genet. 2006 Jun;69(6):504-11. doi: 10.1111/j.1399-0004.2006.00621.x. Clin Genet. 2006. PMID: 16712702

7

The genetic basis of Brugada syndrome: a mutation update.

Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M. Hedley PL, et al. Among authors: kanters jk. Hum Mutat. 2009 Sep;30(9):1256-66. doi: 10.1002/humu.21066. Hum Mutat. 2009. PMID: 19606473 Review.

8

The genetic basis of long QT and short QT syndromes: a mutation update.

Hedley PL, Jørgensen P, Schlamowitz S, Wangari R, Moolman-Smook J, Brink PA, Kanters JK, Corfield VA, Christiansen M. Hedley PL, et al. Among authors: kanters jk. Hum Mutat. 2009 Nov;30(11):1486-511. doi: 10.1002/humu.21106. Hum Mutat. 2009. PMID: 19862833 Review.

9

[Short QT syndrome as an inherited condition].

Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Møller DV, et al. Ugeskr Laeger. 2011 Feb 7;173(6):420-4. Ugeskr Laeger. 2011. PMID: 21299935 Review. Danish.

10

Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model.

Aidt FH, Nielsen SM, Kanters J, Pesta D, Nielsen TT, Nørremølle A, Hasholt L, Christiansen M, Hagen CM. Aidt FH, et al. PLoS Curr. 2013 Apr 2;5:ecurrents.hd.d8917b4862929772c5a2f2a34ef1c201. doi: 10.1371/currents.hd.d8917b4862929772c5a2f2a34ef1c201. PLoS Curr. 2013. PMID: 23568011 Free PMC article.

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