Larsen LA - Search Results

1

Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.

Zhang L, Tümer Z, Møllgård K, Barbi G, Rossier E, Bendsen E, Møller RS, Ullmann R, He J, Papadopoulos N, Tommerup N, Larsen LA. Zhang L, et al. Among authors: larsen la. Eur J Hum Genet. 2009 Aug;17(8):1010-8. doi: 10.1038/ejhg.2008.269. Epub 2009 Jan 28. Eur J Hum Genet. 2009. PMID: 19172993 Free PMC article.

2

The Hedgehog signaling pathway--implications for drug targets in cancer and neurodegenerative disorders.

Bak M, Hansen C, Tommerup N, Larsen LA. Bak M, et al. Among authors: larsen la. Pharmacogenomics. 2003 Jul;4(4):411-29. doi: 10.1517/phgs.4.4.411.22751. Pharmacogenomics. 2003. PMID: 12831321 Review.

3

Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome family.

Henriksen AM, Tümer Z, Tommerup N, Tranebjaerg L, Larsen LA. Henriksen AM, et al. Among authors: larsen la. Genet Test. 2004 Winter;8(4):404-6. doi: 10.1089/gte.2004.8.404. Genet Test. 2004. PMID: 15684871

4

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome.

Boonen SE, Stahl D, Kreiborg S, Rosenberg T, Kalscheuer V, Larsen LA, Tommerup N, Brøndum-Nielsen K, Tümer Z. Boonen SE, et al. Among authors: larsen la. Am J Med Genet A. 2005 Jan 30;132A(3):324-8. doi: 10.1002/ajmg.a.30422. Am J Med Genet A. 2005. PMID: 15690381 Review.

5

Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome.

Tümer Z, Henriksen AM, Bache I, Brixen K, Kalscheuer V, Illum N, Rasmussen K, Larsen LA, Tommerup N. Tümer Z, et al. Among authors: larsen la. Am J Med Genet A. 2005 Jun 15;135(3):339-41. doi: 10.1002/ajmg.a.30735. Am J Med Genet A. 2005. PMID: 15887263 No abstract available.

6

Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease.

Baekvad-Hansen M, Tümer Z, Delicado A, Erdogan F, Tommerup N, Larsen LA. Baekvad-Hansen M, et al. Among authors: larsen la. Am J Med Genet A. 2006 Mar 1;140(5):427-33. doi: 10.1002/ajmg.a.31087. Am J Med Genet A. 2006. PMID: 16470726

7

Hedgehog signaling in small-cell lung cancer: frequent in vivo but a rare event in vitro.

Vestergaard J, Pedersen MW, Pedersen N, Ensinger C, Tümer Z, Tommerup N, Poulsen HS, Larsen LA. Vestergaard J, et al. Among authors: larsen la. Lung Cancer. 2006 Jun;52(3):281-90. doi: 10.1016/j.lungcan.2005.12.014. Epub 2006 Apr 17. Lung Cancer. 2006. PMID: 16616798

8

Evaluation of two methods for generating cRNA for microarray experiments from nanogram amounts of total RNA.

Bak M, Conley L, Hedegaard J, Larsen LA, Sørensen P, Bendixen C, Tommerup N. Bak M, et al. Among authors: larsen la. Anal Biochem. 2006 Nov 1;358(1):111-9. doi: 10.1016/j.ab.2006.08.023. Epub 2006 Sep 7. Anal Biochem. 2006. PMID: 16996470

9

Screening of 99 Danish patients with congenital heart disease for GATA4 mutations.

Zhang L, Tümer Z, Jacobsen JR, Andersen PS, Tommerup N, Larsen LA. Zhang L, et al. Among authors: larsen la. Genet Test. 2006 Winter;10(4):277-80. doi: 10.1089/gte.2006.10.277. Genet Test. 2006. PMID: 17253934

10

Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2.

Jakobsen LP, Ullmann R, Christensen SB, Jensen KE, Mølsted K, Henriksen KF, Hansen C, Knudsen MA, Larsen LA, Tommerup N, Tümer Z. Jakobsen LP, et al. Among authors: larsen la. J Med Genet. 2007 Jun;44(6):381-6. doi: 10.1136/jmg.2006.046177. J Med Genet. 2007. PMID: 17551083 Free PMC article.

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