PubMed for id: 1676318353

Year	Number of Results
1993	1
1994	2
1996	2
2003	1
2004	1
2007	1
2008	1
2010	1
2020	1
2024	0

1

Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.

Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J, Riechers SP, Jain S, Coughlin M, Fontaine JF, Freibaum BD, Brusendorf L, Zenkner M, Porras P, Stroedicke M, Schnoegl S, Arnsburg K, Boeddrich A, Pigazzini L, Heutink P, Taylor JP, Kirstein J, Andrade-Navarro MA, Sharan R, Wanker EE. Haenig C, et al. Cell Rep. 2020 Aug 18;32(7):108050. doi: 10.1016/j.celrep.2020.108050. Cell Rep. 2020. PMID: 32814053 Free article.

2

Identification of differentially expressed genes using an annealing control primer system in stage III serous ovarian carcinoma.

Kim YS, Hwan JD, Bae S, Bae DH, Shick WA. Kim YS, et al. BMC Cancer. 2010 Oct 22;10:576. doi: 10.1186/1471-2407-10-576. BMC Cancer. 2010. PMID: 20969748 Free PMC article.

3

Human chromosome fragility.

Lukusa T, Fryns JP. Lukusa T, et al. Biochim Biophys Acta. 2008 Jan;1779(1):3-16. doi: 10.1016/j.bbagrm.2007.10.005. Epub 2007 Dec 3. Biochim Biophys Acta. 2008. PMID: 18078840 Review.

4

Cloning of a novel neuronally expressed orphan G-protein-coupled receptor which is up-regulated by erythropoietin, interacts with microtubule-associated protein 1b and colocalizes with the 5-hydroxytryptamine 2a receptor.

Maurer MH, Grünewald S, Gassler N, Rossner M, Propst F, Würz R, Weber D, Kuner T, Kuschinsky W, Schneider A. Maurer MH, et al. J Neurochem. 2004 Nov;91(4):1007-17. doi: 10.1111/j.1471-4159.2004.02799.x. J Neurochem. 2004. PMID: 15525354 Free article.

5

Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders.

Steiner CE, Guerreiro MM, Marques-de-Faria AP. Steiner CE, et al. Arq Neuropsiquiatr. 2003 Jun;61(2A):176-80. doi: 10.1590/s0004-282x2003000200003. Epub 2003 Jun 9. Arq Neuropsiquiatr. 2003. PMID: 12806492 Free article.

6

Trinucleotide repeats at the FRAXF locus: frequency and distribution in the general population.

Holden JJ, Walker M, Chalifoux M, White BN. Holden JJ, et al. Am J Med Genet. 1996 Aug 9;64(2):424-7. doi: 10.1002/(SICI)1096-8628(19960809)64:2<424::AID-AJMG38>3.0.CO;2-F. Am J Med Genet. 1996. PMID: 8844097

7

Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.

Holden JJ, Wing M, Chalifoux M, Julien-Inalsingh C, Schutz C, Robinson P, Szatmari P, White BN. Holden JJ, et al. Am J Med Genet. 1996 Aug 9;64(2):399-403. doi: 10.1002/(SICI)1096-8628(19960809)64:2<399::AID-AJMG33>3.0.CO;2-8. Am J Med Genet. 1996. PMID: 8844091

8

The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.

Hirst MC, Barnicoat A, Flynn G, Wang Q, Daker M, Buckle VJ, Davies KE, Bobrow M. Hirst MC, et al. Hum Mol Genet. 1993 Feb;2(2):197-200. doi: 10.1093/hmg/2.2.197. Hum Mol Genet. 1993. PMID: 8499907

9

The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

Ritchie RJ, Knight SJ, Hirst MC, Grewal PK, Bobrow M, Cross GS, Davies KE. Ritchie RJ, et al. Hum Mol Genet. 1994 Dec;3(12):2115-21. doi: 10.1093/hmg/3.12.2115. Hum Mol Genet. 1994. PMID: 7881407

10

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL. Parrish JE, et al. Nat Genet. 1994 Nov;8(3):229-35. doi: 10.1038/ng1194-229. Nat Genet. 1994. PMID: 7874164

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