Lalioti MD - Search Results

1

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: lalioti md. Nat Genet. 1997 Dec;17(4):393-8. doi: 10.1038/ng1297-393. Nat Genet. 1997. PMID: 9398839

2

The human lanosterol synthase gene maps to chromosome 21q22.3.

Young M, Chen H, Lalioti MD, Antonarakis SE. Young M, et al. Among authors: lalioti md. Hum Genet. 1996 May;97(5):620-4. doi: 10.1007/BF02281872. Hum Genet. 1996. PMID: 8655142

3

Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.

Chen H, Rossier C, Lalioti MD, Lynn A, Chakravarti A, Perrin G, Antonarakis SE. Chen H, et al. Among authors: lalioti md. Am J Hum Genet. 1996 Jul;59(1):66-75. Am J Hum Genet. 1996. PMID: 8659545 Free PMC article.

4

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. Nature. 1997 Apr 24;386(6627):847-51. doi: 10.1038/386847a0. Nature. 1997. PMID: 9126745

5

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. Among authors: lalioti md. Hum Genet. 1997 May;99(5):616-23. doi: 10.1007/s004390050416. Hum Genet. 1997. PMID: 9150728

6

What is expanded in progressive myoclonus epilepsy?

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

7

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. Among authors: lalioti md. Genomics. 1998 Jan 1;47(1):64-70. doi: 10.1006/geno.1997.5066. Genomics. 1998. PMID: 9465297

8

Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins.

Scott HS, Heino M, Peterson P, Mittaz L, Lalioti MD, Betterle C, Cohen A, Seri M, Lerone M, Romeo G, Collin P, Salo M, Metcalfe R, Weetman A, Papasavvas MP, Rossier C, Nagamine K, Kudoh J, Shimizu N, Krohn KJ, Antonarakis SE. Scott HS, et al. Among authors: lalioti md. Mol Endocrinol. 1998 Aug;12(8):1112-9. doi: 10.1210/mend.12.8.0143. Mol Endocrinol. 1998. PMID: 9717837

9

Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2).

Scott HS, Antonarakis SE, Lalioti MD, Rossier C, Silver PA, Henry MF. Scott HS, et al. Among authors: lalioti md. Genomics. 1998 Mar 15;48(3):330-40. doi: 10.1006/geno.1997.5190. Genomics. 1998. PMID: 9545638

10

Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequence.

Guipponi M, Scott HS, Kudoh J, Kawasaki K, Shibuya K, Shintani A, Asakawa S, Chen H, Lalioti MD, Rossier C, Minoshima S, Shimizu N, Antonarakis SE. Guipponi M, et al. Among authors: lalioti md. Hum Genet. 1998 Oct;103(4):386-92. doi: 10.1007/s004390050838. Hum Genet. 1998. PMID: 9856478

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