Swango KL[Author] - Search Results

Year	Number of Results
1997	1
1998	2
2000	2
2001	1
2005	2
2006	2
2007	2
2008	1
2014	1
2024	0

1

Partial biotinidase deficiency is usually due to the D444H mutation in the biotinidase gene.

Swango KL, Demirkol M, Hüner G, Pronicka E, Sykut-Cegielska J, Schulze A, Mayatepek E, Wolf B. Swango KL, et al. Hum Genet. 1998 May;102(5):571-5. doi: 10.1007/s004390050742. Hum Genet. 1998. PMID: 9654207

2

A quantitative PCR assay for the assessment of DNA degradation in forensic samples.

Swango KL, Timken MD, Chong MD, Buoncristiani MR. Swango KL, et al. Forensic Sci Int. 2006 Apr 20;158(1):14-26. doi: 10.1016/j.forsciint.2005.04.034. Epub 2005 Jun 3. Forensic Sci Int. 2006. PMID: 15936161

3

Amino acid homologies between human biotinidase and bacterial aliphatic amidases: putative identification of the active site of biotinidase.

Swango KL, Hymes J, Brown P, Wolf B. Swango KL, et al. Mol Genet Metab. 2000 Feb;69(2):111-5. doi: 10.1006/mgme.2000.2959. Mol Genet Metab. 2000. PMID: 10720437

4

Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations.

Blanton SH, Pandya A, Landa BL, Javaheri R, Xia X, Nance WE, Pomponio RJ, Norrgard KJ, Swango KL, Demirkol M, Gülden H, Coskun T, Tokatli A, Ozalp I, Wolf B. Blanton SH, et al. Among authors: swango kl. Hum Hered. 2000 Mar-Apr;50(2):102-11. doi: 10.1159/000022897. Hum Hered. 2000. PMID: 10799968

5

A quadruplex real-time qPCR assay for the simultaneous assessment of total human DNA, human male DNA, DNA degradation and the presence of PCR inhibitors in forensic samples: a diagnostic tool for STR typing.

Hudlow WR, Chong MD, Swango KL, Timken MD, Buoncristiani MR. Hudlow WR, et al. Among authors: swango kl. Forensic Sci Int Genet. 2008 Mar;2(2):108-25. doi: 10.1016/j.fsigen.2007.09.001. Epub 2007 Nov 26. Forensic Sci Int Genet. 2008. PMID: 19083806

6

Developmental validation of a multiplex qPCR assay for assessing the quantity and quality of nuclear DNA in forensic samples.

Swango KL, Hudlow WR, Timken MD, Buoncristiani MR. Swango KL, et al. Forensic Sci Int. 2007 Jul 20;170(1):35-45. doi: 10.1016/j.forsciint.2006.09.002. Epub 2006 Oct 30. Forensic Sci Int. 2007. PMID: 17071034

7

Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online.

Norrgard KJ, Pomponio RJ, Swango KL, Hymes J, Reynolds T, Buck GA, Wolf B. Norrgard KJ, et al. Among authors: swango kl. Hum Mutat. 1998;11(5):410. doi: 10.1002/(SICI)1098-1004(1998)11:5<410::AID-HUMU10>3.0.CO;2-8. Hum Mutat. 1998. PMID: 10206677

8

Conservation of biotindase in mammals and identification of the putative biotinidase gene in Drosophila melanogaster.

Swango KL, Wolf B. Swango KL, et al. Mol Genet Metab. 2001 Dec;74(4):492-9. doi: 10.1006/mgme.2001.3244. Mol Genet Metab. 2001. PMID: 11749055

9

Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States.

Norrgard KJ, Pomponio RJ, Swango KL, Hymes J, Reynolds TR, Buck GA, Wolf B. Norrgard KJ, et al. Among authors: swango kl. Biochem Mol Med. 1997 Jun;61(1):22-7. doi: 10.1006/bmme.1997.2597. Biochem Mol Med. 1997. PMID: 9232193

10

Developmental validation of the PowerPlex(®) Fusion System for analysis of casework and reference samples: A 24-locus multiplex for new database standards.

Oostdik K, Lenz K, Nye J, Schelling K, Yet D, Bruski S, Strong J, Buchanan C, Sutton J, Linner J, Frazier N, Young H, Matthies L, Sage A, Hahn J, Wells R, Williams N, Price M, Koehler J, Staples M, Swango KL, Hill C, Oyerly K, Duke W, Katzilierakis L, Ensenberger MG, Bourdeau JM, Sprecher CJ, Krenke B, Storts DR. Oostdik K, et al. Among authors: swango kl. Forensic Sci Int Genet. 2014 Sep;12:69-76. doi: 10.1016/j.fsigen.2014.04.013. Epub 2014 May 14. Forensic Sci Int Genet. 2014. PMID: 24905335 Free article.

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