Scott HS - Search Results

1

Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome.

Chrast R, Scott HS, Madani R, Huber L, Wolfer DP, Prinz M, Aguzzi A, Lipp HP, Antonarakis SE. Chrast R, et al. Among authors: scott hs. Hum Mol Genet. 2000 Jul 22;9(12):1853-64. doi: 10.1093/hmg/9.12.1853. Hum Mol Genet. 2000. PMID: 10915774 Free article.

2

Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy.

Lalioti MD, Scott HS, Buresi C, Rossier C, Bottani A, Morris MA, Malafosse A, Antonarakis SE. Lalioti MD, et al. Among authors: scott hs. Nature. 1997 Apr 24;386(6627):847-51. doi: 10.1038/386847a0. Nature. 1997. PMID: 9126745

3

Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3.

Mittaz L, Scott HS, Rossier C, Seeburg PH, Higuchi M, Antonarakis SE. Mittaz L, et al. Among authors: scott hs. Genomics. 1997 Apr 15;41(2):210-7. doi: 10.1006/geno.1997.4655. Genomics. 1997. PMID: 9143496

4

Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3.

Scott HS, Chen H, Rossier C, Lalioti MD, Antonarakis SE. Scott HS, et al. Hum Genet. 1997 May;99(5):616-23. doi: 10.1007/s004390050416. Hum Genet. 1997. PMID: 9150728

5

Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal region.

Chrast R, Scott HS, Chen H, Kudoh J, Rossier C, Minoshima S, Wang Y, Shimizu N, Antonarakis SE. Chrast R, et al. Among authors: scott hs. Genome Res. 1997 Jun;7(6):615-24. doi: 10.1101/gr.7.6.615. Genome Res. 1997. PMID: 9199934 Free PMC article.

6

Localization of a novel human RNA-editing deaminase (hRED2 or ADARB2) to chromosome 10p15.

Mittaz L, Antonarakis SE, Higuchi M, Scott HS. Mittaz L, et al. Among authors: scott hs. Hum Genet. 1997 Sep;100(3-4):398-400. doi: 10.1007/s004390050523. Hum Genet. 1997. PMID: 9272162

7

What is expanded in progressive myoclonus epilepsy?

Lalioti MD, Scott HS, Antonarakis SE. Lalioti MD, et al. Among authors: scott hs. Nat Genet. 1997 Sep;17(1):17. doi: 10.1038/ng0997-17. Nat Genet. 1997. PMID: 9288090 No abstract available.

8

Positional cloning of the APECED gene.

Nagamine K, Peterson P, Scott HS, Kudoh J, Minoshima S, Heino M, Krohn KJ, Lalioti MD, Mullis PE, Antonarakis SE, Kawasaki K, Asakawa S, Ito F, Shimizu N. Nagamine K, et al. Among authors: scott hs. Nat Genet. 1997 Dec;17(4):393-8. doi: 10.1038/ng1297-393. Nat Genet. 1997. PMID: 9398839

9

Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis.

Scott HS, Kyriakou DS, Peterson P, Heino M, Tähtinen M, Krohn K, Chen H, Rossier C, Lalioti MD, Antonarakis SE. Scott HS, et al. Genomics. 1998 Jan 1;47(1):64-70. doi: 10.1006/geno.1997.5066. Genomics. 1998. PMID: 9465297

10

A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset.

Lalioti MD, Scott HS, Genton P, Grid D, Ouazzani R, M'Rabet A, Ibrahim S, Gouider R, Dravet C, Chkili T, Bottani A, Buresi C, Malafosse A, Antonarakis SE. Lalioti MD, et al. Among authors: scott hs. Am J Hum Genet. 1998 Apr;62(4):842-7. doi: 10.1086/301798. Am J Hum Genet. 1998. PMID: 9529356 Free PMC article.

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