Longshore JW - Search Results

1

Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation.

Friez MJ, Essop FB, Krause A, Castiglia L, Ragusa A, Sossey-Alaoui K, Nelson RL, May MM, Michaelis RC, Srivastava AK, Schwartz CE, Stevenson RE, Goldman A, Villard L, Longshore JW. Friez MJ, et al. Among authors: longshore jw. Hum Genet. 2000 Jan;106(1):36-9. doi: 10.1007/s004390051006. Hum Genet. 2000. PMID: 10982179

2

The HOPA gene dodecamer duplication is not a significant etiological factor in autism.

Michaelis RC, Copeland-Yates SA, Sossey-Alaoui K, Skinner C, Friez MJ, Longshore JW, Simensen RJ, Schroer RJ, Stevenson RE. Michaelis RC, et al. Among authors: longshore jw. J Autism Dev Disord. 2000 Aug;30(4):355-8. doi: 10.1023/a:1005583517994. J Autism Dev Disord. 2000. PMID: 11039861

3

Recovery and phylogenetic analysis of nifH sequences from diazotrophic bacteria associated with dead aboveground biomass of Spartina alterniflora.

Lovell CR, Friez MJ, Longshore JW, Bagwell CE. Lovell CR, et al. Among authors: longshore jw. Appl Environ Microbiol. 2001 Nov;67(11):5308-14. doi: 10.1128/AEM.67.11.5308-5314.2001. Appl Environ Microbiol. 2001. PMID: 11679360 Free PMC article.

4

X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.

Amos-Landgraf JM, Cottle A, Plenge RM, Friez M, Schwartz CE, Longshore J, Willard HF. Amos-Landgraf JM, et al. Am J Hum Genet. 2006 Sep;79(3):493-9. doi: 10.1086/507565. Epub 2006 Jul 27. Am J Hum Genet. 2006. PMID: 16909387 Free PMC article.

5

Molecular diversity of diazotrophs in oligotrophic tropical seagrass bed communities.

Bagwell CE, Rocque JR, Smith GW, Polson SW, Friez MJ, Longshore JW, Lovell CR. Bagwell CE, et al. Among authors: longshore jw. FEMS Microbiol Ecol. 2002 Feb 1;39(2):113-9. doi: 10.1111/j.1574-6941.2002.tb00912.x. FEMS Microbiol Ecol. 2002. PMID: 19709190 Free article.

6

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.

Nolin SL, Brown WT, Glicksman A, Houck GE Jr, Gargano AD, Sullivan A, Biancalana V, Bröndum-Nielsen K, Hjalgrim H, Holinski-Feder E, Kooy F, Longshore J, Macpherson J, Mandel JL, Matthijs G, Rousseau F, Steinbach P, Väisänen ML, von Koskull H, Sherman SL. Nolin SL, et al. Am J Hum Genet. 2003 Feb;72(2):454-64. doi: 10.1086/367713. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529854 Free PMC article.

7

Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.

Brown TC, Tarleton JC, Go RC, Longshore JW, Descartes M. Brown TC, et al. Among authors: longshore jw. Am J Med Genet. 1997 Dec 31;73(4):447-55. doi: 10.1002/(sici)1096-8628(19971231)73:4<447::aid-ajmg14>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9415473

8

Terminal deletion of the long arm of chromosome 4 in a mother and two sons.

Descartes M, Keppler-Noreuil K, Knops J, Longshore JW, Finley WH, Carroll AJ. Descartes M, et al. Among authors: longshore jw. Clin Genet. 1996 Dec;50(6):538-40. doi: 10.1111/j.1399-0004.1996.tb02733.x. Clin Genet. 1996. PMID: 9147894 Review.

9

Tissue-specific methylation differences in a fragile X premutation carrier.

Tassone F, Longshore J, Zunich J, Steinbach P, Salat U, Taylor AK. Tassone F, et al. Clin Genet. 1999 May;55(5):346-51. doi: 10.1034/j.1399-0004.1999.550508.x. Clin Genet. 1999. PMID: 10422805

10

Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome.

Han J, Hsu C, Zhu Z, Longshore JW, Finley WH. Han J, et al. Among authors: longshore jw. Nucleic Acids Res. 1994 May 11;22(9):1735-40. doi: 10.1093/nar/22.9.1735. Nucleic Acids Res. 1994. PMID: 8202379 Free PMC article.

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