Jeremiah S - Search Results

1

Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray.

Ekong R, Jeremiah S, Judah D, Lehmann O, Mirzayans F, Hung YC, Walter MA, Bhattacharya S, Gant TW, Povey S, Wolfe J. Ekong R, et al. Among authors: jeremiah s. Hum Mutat. 2004 Jul;24(1):76-85. doi: 10.1002/humu.20059. Hum Mutat. 2004. PMID: 15221791

2

Mapping ESTs to the TSC1 candidate interval by use of the 'Science 96' transcript map.

Wolfe J, Jeremiah S, Young J, Burley MW, Stewart H, McCulley M, Grant C, Naz K, Povey S. Wolfe J, et al. Among authors: jeremiah s. Ann Hum Genet. 1997 Sep;61(Pt 5):401-9. doi: 10.1046/j.1469-1809.1997.6150401.x. Ann Hum Genet. 1997. PMID: 9459002

3

A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients.

Young JM, Burley MW, Jeremiah SJ, Jeganathan D, Ekong R, Osborne JP, Povey S. Young JM, et al. Among authors: jeremiah sj. Ann Hum Genet. 1998 May;62(Pt 3):203-13. doi: 10.1046/j.1469-1809.1998.6230203.x. Ann Hum Genet. 1998. PMID: 9803264

4

Chromosomal localisation of genes coding for human and mouse liver cytosolic cysteine dioxygenase.

Jeremiah S, McCann KP, Williams AC, Ramsden DB, Pilz AJ, Fox MF, Povey S. Jeremiah S, et al. Ann Hum Genet. 1996 Jan;60(1):29-33. doi: 10.1111/j.1469-1809.1996.tb01169.x. Ann Hum Genet. 1996. PMID: 8835096

5

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

Povey S, Burley MW, Attwood J, Benham F, Hunt D, Jeremiah SJ, Franklin D, Gillett G, Malas S, Robson EB. Povey S, et al. Among authors: jeremiah sj. Ann Hum Genet. 1994 May;58(2):107-27. doi: 10.1111/j.1469-1809.1994.tb01881.x. Ann Hum Genet. 1994. PMID: 7979156

6

The assignment of the human gene coding for complement C5 to chromosome 9q22-9q33.

Jeremiah SJ, West LF, Davis M, Povey S, Carritt B, Fey GH. Jeremiah SJ, et al. Ann Hum Genet. 1988 May;52(2):111-6. doi: 10.1111/j.1469-1809.1988.tb01085.x. Ann Hum Genet. 1988. PMID: 3248005

7

Localization of the Tamm-Horsfall glycoprotein (uromodulin) gene to chromosome 16p12.3-16p13.11.

Pook MA, Jeremiah S, Scheinman SJ, Povey S, Thakker RV. Pook MA, et al. Among authors: jeremiah s. Ann Hum Genet. 1993 Oct;57(4):285-90. doi: 10.1111/j.1469-1809.1993.tb00902.x. Ann Hum Genet. 1993. PMID: 8179291

8

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.

van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, Lindhout D, van den Ouweland A, Halley D, Young J, Burley M, Jeremiah S, Woodward K, Nahmias J, Fox M, Ekong R, Osborne J, Wolfe J, Povey S, Snell RG, Cheadle JP, Jones AC, Tachataki M, Ravine D, Sampson JR, Reeve MP, Richardson P, Wilmer F, Munro C, Hawkins TL, Sepp T, Ali JB, Ward S, Green AJ, Yates JR, Kwiatkowska J, Henske EP, Short MP, Haines JH, Jozwiak S, Kwiatkowski DJ. van Slegtenhorst M, et al. Among authors: jeremiah s. Science. 1997 Aug 8;277(5327):805-8. doi: 10.1126/science.277.5327.805. Science. 1997. PMID: 9242607

9

The assignment of the genes coding for human complement components C6 and C7 to chromosome 5.

Jeremiah SJ, Abbott CM, Murad Z, Povey S, Thomas HJ, Solomon E, DiScipio RG, Fey GH. Jeremiah SJ, et al. Ann Hum Genet. 1990 May;54(2):141-7. doi: 10.1111/j.1469-1809.1990.tb00370.x. Ann Hum Genet. 1990. PMID: 2382968

10

The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction.

Abbott C, West L, Povey S, Jeremiah S, Murad Z, DiScipio R, Fey G. Abbott C, et al. Among authors: jeremiah s. Genomics. 1989 May;4(4):606-9. doi: 10.1016/0888-7543(89)90286-3. Genomics. 1989. PMID: 2744767

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