South ST - Search Results

1

Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome.

Kahlem P, Sultan M, Herwig R, Steinfath M, Balzereit D, Eppens B, Saran NG, Pletcher MT, South ST, Stetten G, Lehrach H, Reeves RH, Yaspo ML. Kahlem P, et al. Among authors: south st. Genome Res. 2004 Jul;14(7):1258-67. doi: 10.1101/gr.1951304. Genome Res. 2004. PMID: 15231742 Free PMC article.

2

Long-range chromosomal engineering is more efficient in vitro than in vivo.

Olson LE, Tien J, South S, Reeves RH. Olson LE, et al. Transgenic Res. 2005 Jun;14(3):325-32. doi: 10.1007/s11248-005-0389-6. Transgenic Res. 2005. PMID: 16145840

3

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes.

Ou Z, Stankiewicz P, Xia Z, Breman AM, Dawson B, Wiszniewska J, Szafranski P, Cooper ML, Rao M, Shao L, South ST, Coleman K, Fernhoff PM, Deray MJ, Rosengren S, Roeder ER, Enciso VB, Chinault AC, Patel A, Kang SH, Shaw CA, Lupski JR, Cheung SW. Ou Z, et al. Among authors: south st. Genome Res. 2011 Jan;21(1):33-46. doi: 10.1101/gr.111609.110. Genome Res. 2011. PMID: 21205869 Free PMC article.

4

Prenatal detection of an interstitial deletion in 4p15 in a fetus with an increased nuchal skin fold measurement.

South ST, Corson VL, McMichael JL, Blakemore KJ, Stetten G. South ST, et al. Fetal Diagn Ther. 2005 Jan-Feb;20(1):58-63. doi: 10.1159/000081371. Fetal Diagn Ther. 2005. PMID: 15608462 Review.

5

A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.

Boyadjiev SA, South ST, Radford CL, Patel A, Zhang G, Hur DJ, Thomas GH, Gearhart JP, Stetten G. Boyadjiev SA, et al. Among authors: south st. Genomics. 2005 May;85(5):622-9. doi: 10.1016/j.ygeno.2005.01.002. Genomics. 2005. PMID: 15820314

6

Reevaluating confined placental mosaicism.

Stetten G, Escallon CS, South ST, McMichael JL, Saul DO, Blakemore KJ. Stetten G, et al. Among authors: south st. Am J Med Genet A. 2004 Dec 15;131(3):232-9. doi: 10.1002/ajmg.a.30363. Am J Med Genet A. 2004. PMID: 15529330

7

In utero hematopoietic stem cell transplantation with haploidentical donor adult bone marrow in a canine model.

Blakemore K, Hattenburg C, Stetten G, Berg K, South S, Murphy K, Jones R. Blakemore K, et al. Am J Obstet Gynecol. 2004 Apr;190(4):960-73. doi: 10.1016/j.ajog.2004.01.014. Am J Obstet Gynecol. 2004. PMID: 15118622

8

Mapping of mutation causing Friedreich's ataxia to human chromosome 9.

Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, von Gabain A, Farrall M, Williamson R. Chamberlain S, et al. Nature. 1988 Jul 21;334(6179):248-50. doi: 10.1038/334248a0. Nature. 1988. PMID: 2899844

9

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.

South ST, Whitby H, Maxwell T, Aston E, Brothman AR, Carey JC. South ST, et al. Am J Med Genet A. 2008 Oct 15;146A(20):2691-7. doi: 10.1002/ajmg.a.32516. Am J Med Genet A. 2008. PMID: 18798325

10

Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome.

Andersen EF, Carey JC, Earl DL, Corzo D, Suttie M, Hammond P, South ST. Andersen EF, et al. Among authors: south st. Eur J Hum Genet. 2014 Apr;22(4):464-70. doi: 10.1038/ejhg.2013.192. Epub 2013 Aug 21. Eur J Hum Genet. 2014. PMID: 23963300 Free PMC article.

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