Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 24

1.

STRmix™ collaborative exercise on DNA mixture interpretation.

Bright JA, Cheng K, Kerr Z, McGovern C, Kelly H, Moretti TR, Smith MA, Bieber FR, Budowle B, Coble MD, Alghafri R, Allen PS, Barber A, Beamer V, Buettner C, Russell M, Gehrig C, Hicks T, Charak J, Cheong-Wing K, Ciecko A, Davis CT, Donley M, Pedersen N, Gartside B, Granger D, Greer-Ritzheimer M, Reisinger E, Kennedy J, Grammer E, Kaplan M, Hansen D, Larsen HJ, Laureano A, Li C, Lien E, Lindberg E, Kelly C, Mallinder B, Malsom S, Yacovone-Margetts A, McWhorter A, Prajapati SM, Powell T, Shutler G, Stevenson K, Stonehouse AR, Smith L, Murakami J, Halsing E, Wright D, Clark L, Taylor DA, Buckleton J.

Forensic Sci Int Genet. 2019 May;40:1-8. doi: 10.1016/j.fsigen.2019.01.006. Epub 2019 Jan 15.

PMID:
30665115
2.

Genetic anomalies consistent with gonadal mosaicism encountered in a sexual assault-homicide.

Shutler G, Roy T.

Forensic Sci Int Genet. 2012 Dec;6(6):e159-60. doi: 10.1016/j.fsigen.2012.04.003. Epub 2012 Aug 28. No abstract available.

PMID:
22939084
3.

A simple DNA extraction method for marijuana samples used in amplified fragment length polymorphism (AFLP) analysis.

Miller Coyle H, Shutler G, Abrams S, Hanniman J, Neylon S, Ladd C, Palmbach T, Lee HC.

J Forensic Sci. 2003 Mar;48(2):343-7.

PMID:
12664992
4.

Analysis of salivary DNA evidence from a bite mark on a body submerged in water.

Sweet D, Shutler GG.

J Forensic Sci. 1999 Sep;44(5):1069-72.

PMID:
10486961
5.

Removal of a PCR inhibitor and resolution of DNA STR types in mixed human-canine stains from a five year old case.

Shutler GG, Gagnon P, Verret G, Kalyn H, Korkosh S, Johnston E, Halverson J.

J Forensic Sci. 1999 May;44(3):623-6.

PMID:
10408119
6.

Genomic structure of the human D-site binding protein (DBP) gene.

Shutler G, Glassco T, Kang X, Korneluk R, Mueller CR.

Genomics. 1996 Jun 15;34(3):334-9.

PMID:
8786133
7.

Isolation of a novel G protein-coupled receptor (GPR4) localized to chromosome 19q13.3.

Mahadevan MS, Baird S, Bailly JE, Shutler GG, Sabourin LA, Tsilfidis C, Neville CE, Narang M, Korneluk RG.

Genomics. 1995 Nov 1;30(1):84-8.

PMID:
8595909
8.

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy.

Roy N, Mahadevan MS, McLean M, Shutler G, Yaraghi Z, Farahani R, Baird S, Besner-Johnston A, Lefebvre C, Kang X, et al.

Cell. 1995 Jan 13;80(1):167-78.

9.

The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.

Shutler GG, MacKenzie AE, Korneluk RG.

Am J Hum Genet. 1994 Jan;54(1):104-13.

10.

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

Shutler G, Korneluk RG, Tsilfidis C, Mahadevan M, Bailly J, Smeets H, Jansen G, Wieringa B, Lohman F, Aslanidis C, et al.

Genomics. 1992 Jul;13(3):518-25.

PMID:
1639380
11.

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barceló J, O'Hoy K, et al.

Science. 1992 Mar 6;255(5049):1253-5.

PMID:
1546325
12.

Cloning of the essential myotonic dystrophy region and mapping of the putative defect.

Aslanidis C, Jansen G, Amemiya C, Shutler G, Mahadevan M, Tsilfidis C, Chen C, Alleman J, Wormskamp NG, Vooijs M, et al.

Nature. 1992 Feb 6;355(6360):548-51.

PMID:
1346925
13.

Simple, rapid detection of PCR heteroduplexes in DNA mutations and polymorphisms.

Surh LC, Shutler GG, Korneluk RG.

Clin Chem. 1991 Dec;37(12):2142. No abstract available.

PMID:
1764797
14.

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

Tsilfidis C, MacKenzie AE, Shutler G, Leblond S, Bailly J, Johnson K, Williamson R, Siegel-Bartelt J, Korneluk RG, Shelbourne P.

Am J Hum Genet. 1991 Nov;49(5):961-5. Erratum in: Am J Hum Genet 1992 Mar;50(3):659.

15.

An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3.

Shutler G, Leblond S, Bailly J, MacKenzie AE, Tsilfidis C, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1159. No abstract available.

16.

RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3.

Shutler G, Tsilfidis C, Leblond S, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1158. No abstract available.

17.

An SstI RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3.

Tsilfidis C, Shutler G, Leblond S, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1158. No abstract available.

18.

A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119).

Korneluk RG, Tsilfidis C, Shutler G, Mahadevan M, Bailly J, Surh LC.

Nucleic Acids Res. 1991 Mar 11;19(5):1157. No abstract available.

19.

A frequent HincII polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118).

Tsilfidis C, Shutler G, Mahadevan M, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1157. No abstract available.

20.

Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.

Shutler G, MacKenzie AE, Brunner H, Wieringa B, de Jong P, Lohman FP, Leblond S, Bailly J, Korneluk RG.

Genomics. 1991 Mar;9(3):500-4.

PMID:
1674498
21.
22.

A simple and sensitive method for quantifying human genomic DNA in forensic specimen extracts.

Waye JS, Presley LA, Budowle B, Shutler GG, Fourney RM.

Biotechniques. 1989 Sep;7(8):852-5.

PMID:
2631790
23.
24.

The effects of experimental inflammation on adaptive synthesis of rat liver fatty acid synthetase.

Shutler GG, Langstaff JM, Jamieson JC, Burton DN.

Arch Biochem Biophys. 1977 Oct;183(2):710-7. No abstract available.

PMID:
921282

Supplemental Content

Loading ...
Support Center