Hoyle J - Search Results

1

Localization of human and mouse N-ethylmaleimide-sensitive factor (NSF) gene: a two-domain member of the AAA family that is involved in membrane fusion.

Hoyle J, Phelan JP, Bermingham N, Fisher EM. Hoyle J, et al. Mamm Genome. 1996 Nov;7(11):850-2. doi: 10.1007/s003359900249. Mamm Genome. 1996. PMID: 8875895 No abstract available.

2

The gene encoding tripeptidyl peptidase II maps to chromosome 1 in the mouse.

Bermingham NA, McKay T, Hoyle J, Hernandez D, Martin JE, Fisher EM. Bermingham NA, et al. Among authors: hoyle j. Mamm Genome. 1996 May;7(5):390. doi: 10.1007/BF03035314. Mamm Genome. 1996. PMID: 8661741 No abstract available.

3

Genomic organization and mapping of the mouse P26s4 ATPase gene: a member of the remarkably conserved AAA gene family.

Hoyle J, Fisher EM. Hoyle J, et al. Genomics. 1996 Jan 1;31(1):115-8. doi: 10.1006/geno.1996.0017. Genomics. 1996. PMID: 8808288

4

Mapping the valosin-containing protein (VCP) gene on human chromosome 9 and mouse chromosome 4, and a likely pseudogene on the mouse X chromosome.

Hoyle J, Tan KH, Fisher EM. Hoyle J, et al. Mamm Genome. 1997 Oct;8(10):778-80. doi: 10.1007/s003359900566. Mamm Genome. 1997. PMID: 9321476 No abstract available.

5

The gene that encodes the phosphatidylinositol-3 kinase regulatory subunit (p85 alpha) maps to chromosome 13 in the mouse.

Hoyle J, Yulug IG, Egan SE, Fisher EM. Hoyle J, et al. Genomics. 1994 Nov 15;24(2):400-2. doi: 10.1006/geno.1994.1638. Genomics. 1994. PMID: 7698770 No abstract available.

6

Characterisation of a short interspersed repeat (Mermaid) that has family members on human chromosome 21 and elsewhere in the human genome.

Hoyle J, Yulug IG, Johnstone K, Scambler PJ, Fisher EM. Hoyle J, et al. Hum Genet. 1996 Jan;97(1):117-20. doi: 10.1007/BF00218845. Hum Genet. 1996. PMID: 8557251

7

Localization of genes encoding two human one-domain members of the AAA family: PSMC5 (the thyroid hormone receptor-interacting protein, TRIP1) and PSMC3 (the Tat-binding protein, TBP1).

Hoyle J, Tan KH, Fisher EM. Hoyle J, et al. Hum Genet. 1997 Feb;99(2):285-8. doi: 10.1007/s004390050356. Hum Genet. 1997. PMID: 9048938

8

A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report.

Shangaris P, Ho A, Marnerides A, George S, AlAdnani M, Yau S, Jansson M, Hoyle J, Ahn JW, Ellard S, Irving M, Wellesley D, Pasupathy D, Holder-Espinasse M. Shangaris P, et al. Among authors: hoyle j. BMC Med Genomics. 2021 Feb 26;14(1):58. doi: 10.1186/s12920-021-00901-6. BMC Med Genomics. 2021. PMID: 33637067 Free PMC article.

9

Differential expression of two immediate early genes of herpesvirus saimiri as detected by in situ hybridization.

Hoyle J, Honess RW, Randall RE. Hoyle J, et al. J Gen Virol. 1990 Dec;71 ( Pt 12):3005-8. doi: 10.1099/0022-1317-71-12-3005. J Gen Virol. 1990. PMID: 2177092

10

Dymeclin, the gene underlying Dyggve-Melchior-Clausen syndrome, encodes a protein integral to extracellular matrix and golgi organization and is associated with protein secretion pathways critical in bone development.

Denais C, Dent CL, Southgate L, Hoyle J, Dafou D, Trembath RC, Machado RD. Denais C, et al. Among authors: hoyle j. Hum Mutat. 2011 Feb;32(2):231-9. doi: 10.1002/humu.21413. Hum Mutat. 2011. PMID: 21280149

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