Grewal PK - Search Results

1

The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.

Grewal PK, van Deutekom JC, Mills KA, Lemmers RJ, Mathews KD, Frants RR, Hewitt JE. Grewal PK, et al. Mamm Genome. 1997 Jun;8(6):394-8. doi: 10.1007/s003359900454. Mamm Genome. 1997. PMID: 9166581

2

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.

van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR. van Deutekom JC, et al. Among authors: grewal pk. Hum Mol Genet. 1996 May;5(5):581-90. doi: 10.1093/hmg/5.5.581. Hum Mol Genet. 1996. PMID: 8733123

3

Fath, the murine homolog of the Drosophila fat tumor suppressor gene, maps to chromosome 8.

Grewal PK, Hewitt JE. Grewal PK, et al. Mamm Genome. 1997 May;8(5):383-4. doi: 10.1007/s003359900450. Mamm Genome. 1997. PMID: 9107695 No abstract available.

4

High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint.

Grewal PK, Bolland DJ, Todd LC, Hewitt JE. Grewal PK, et al. Mamm Genome. 1998 Aug;9(8):603-7. doi: 10.1007/s003359900829. Mamm Genome. 1998. PMID: 9680377

5

FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates.

Grewal PK, Todd LC, van der Maarel S, Frants RR, Hewitt JE. Grewal PK, et al. Gene. 1998 Aug 17;216(1):13-9. doi: 10.1016/s0378-1119(98)00334-5. Gene. 1998. PMID: 9714712

6

Recent amplification of the human FRG1 gene during primate evolution.

Grewal PK, van Geel M, Frants RR, de Jong P, Hewitt JE. Grewal PK, et al. Gene. 1999 Feb 4;227(1):79-88. doi: 10.1016/s0378-1119(98)00587-3. Gene. 1999. PMID: 9931447

7

Mutation of Large, which encodes a putative glycosyltransferase, in an animal model of muscular dystrophy.

Grewal PK, Hewitt JE. Grewal PK, et al. Biochim Biophys Acta. 2002 Dec 19;1573(3):216-24. doi: 10.1016/s0304-4165(02)00387-2. Biochim Biophys Acta. 2002. PMID: 12417403 Review.

8

Glycosylation defects: a new mechanism for muscular dystrophy?

Grewal PK, Hewitt JE. Grewal PK, et al. Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R259-64. doi: 10.1093/hmg/ddg272. Epub 2003 Aug 12. Hum Mol Genet. 2003. PMID: 12925572 Review.

9

A search for genes in the facioscapulohumeral muscular dystrophy region.

Grewal PK, Van Deutekom JC, Frants RR, Hewitt JE. Grewal PK, et al. Biochem Soc Trans. 1996 May;24(2):282S. doi: 10.1042/bst024282s. Biochem Soc Trans. 1996. PMID: 8736940 No abstract available.

10

Cloning of the murine unconventional myosin gene Myo9b and identification of alternative splicing.

Grewal PK, Jones AM, Maconochie M, Lemmers RJ, Frants RR, Hewitt JE. Grewal PK, et al. Gene. 1999 Nov 29;240(2):389-98. doi: 10.1016/s0378-1119(99)00459-x. Gene. 1999. PMID: 10580159

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