Walz K - Search Results

1

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

Walz K, Paylor R, Yan J, Bi W, Lupski JR. Walz K, et al. J Clin Invest. 2006 Nov;116(11):3035-41. doi: 10.1172/JCI28953. Epub 2006 Oct 5. J Clin Invest. 2006. PMID: 17024248 Free PMC article.

2

Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse.

Bi W, Yan J, Stankiewicz P, Park SS, Walz K, Boerkoel CF, Potocki L, Shaffer LG, Devriendt K, Nowaczyk MJ, Inoue K, Lupski JR. Bi W, et al. Among authors: walz k. Genome Res. 2002 May;12(5):713-28. doi: 10.1101/gr.73702. Genome Res. 2002. PMID: 11997338 Free PMC article.

3

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

Walz K, Caratini-Rivera S, Bi W, Fonseca P, Mansouri DL, Lynch J, Vogel H, Noebels JL, Bradley A, Lupski JR. Walz K, et al. Mol Cell Biol. 2003 May;23(10):3646-55. doi: 10.1128/MCB.23.10.3646-3655.2003. Mol Cell Biol. 2003. PMID: 12724422 Free PMC article.

4

COP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblast.

Yan J, Walz K, Nakamura H, Carattini-Rivera S, Zhao Q, Vogel H, Wei N, Justice MJ, Bradley A, Lupski JR. Yan J, et al. Among authors: walz k. Mol Cell Biol. 2003 Oct;23(19):6798-808. doi: 10.1128/MCB.23.19.6798-6808.2003. Mol Cell Biol. 2003. PMID: 12972600 Free PMC article.

5

Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2).

Walz K, Spencer C, Kaasik K, Lee CC, Lupski JR, Paylor R. Walz K, et al. Hum Mol Genet. 2004 Feb 15;13(4):367-78. doi: 10.1093/hmg/ddh044. Epub 2004 Jan 6. Hum Mol Genet. 2004. PMID: 14709593

6

Genomic disorders: genome architecture results in susceptibility to DNA rearrangements causing common human traits.

Stankiewicz P, Inoue K, Bi W, Walz K, Park SS, Kurotaki N, Shaw CJ, Fonseca P, Yan J, Lee JA, Khajavi M, Lupski JR. Stankiewicz P, et al. Among authors: walz k. Cold Spring Harb Symp Quant Biol. 2003;68:445-54. doi: 10.1101/sqb.2003.68.445. Cold Spring Harb Symp Quant Biol. 2003. PMID: 15338647 Review. No abstract available.

7

Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome.

Yan J, Keener VW, Bi W, Walz K, Bradley A, Justice MJ, Lupski JR. Yan J, et al. Among authors: walz k. Hum Mol Genet. 2004 Nov 1;13(21):2613-24. doi: 10.1093/hmg/ddh288. Epub 2004 Sep 30. Hum Mol Genet. 2004. PMID: 15459175

8

Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.

Bi W, Saifi GM, Shaw CJ, Walz K, Fonseca P, Wilson M, Potocki L, Lupski JR. Bi W, et al. Among authors: walz k. Hum Genet. 2004 Nov;115(6):515-24. doi: 10.1007/s00439-004-1187-6. Epub 2004 Sep 30. Hum Genet. 2004. PMID: 15565467

9

Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)].

Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, Noebels JL. Goldman AM, et al. Among authors: walz k. J Child Neurol. 2006 Feb;21(2):93-8. doi: 10.1177/08830738060210021201. J Child Neurol. 2006. PMID: 16566870

10

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.

Molina J, Carmona-Mora P, Chrast J, Krall PM, Canales CP, Lupski JR, Reymond A, Walz K. Molina J, et al. Among authors: walz k. Hum Mol Genet. 2008 Aug 15;17(16):2486-95. doi: 10.1093/hmg/ddn148. Epub 2008 May 10. Hum Mol Genet. 2008. PMID: 18469339

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