Li J - Search Results

1

Loss of the proteostasis factor AIRAPL causes myeloid transformation by deregulating IGF-1 signaling.

Osorio FG, Soria-Valles C, Santiago-Fernández O, Bernal T, Mittelbrunn M, Colado E, Rodríguez F, Bonzon-Kulichenko E, Vázquez J, Porta-de-la-Riva M, Cerón J, Fueyo A, Li J, Green AR, Freije JM, López-Otín C. Osorio FG, et al. Among authors: li j. Nat Med. 2016 Jan;22(1):91-6. doi: 10.1038/nm.4013. Epub 2015 Dec 21. Nat Med. 2016. PMID: 26692333

2

Rescue of the lethal scl(-/-) phenotype by the human SCL locus.

Sinclair AM, Bench AJ, Bloor AJ, Li J, Göttgens B, Stanley ML, Miller J, Piltz S, Hunter S, Nacheva EP, Sanchez MJ, Green AR. Sinclair AM, et al. Among authors: li j. Blood. 2002 Jun 1;99(11):3931-8. doi: 10.1182/blood.v99.11.3931. Blood. 2002. PMID: 12010791 Free article.

3

Absence of SCL mutations in myeloid malignancies.

Delabesse E, Li J, Schnittger S, Hiddemann W, Green AR. Delabesse E, et al. Among authors: li j. Br J Haematol. 2003 Feb;120(3):482-3. doi: 10.1046/j.1365-2141.2003.04122.x. Br J Haematol. 2003. PMID: 12580964 Free article.

4

Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies.

Li J, Bench AJ, Vassiliou GS, Fourouclas N, Ferguson-Smith AC, Green AR. Li J, et al. Proc Natl Acad Sci U S A. 2004 May 11;101(19):7341-6. doi: 10.1073/pnas.0308195101. Epub 2004 Apr 30. Proc Natl Acad Sci U S A. 2004. PMID: 15123827 Free PMC article.

5

Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies.

Bench AJ, Li J, Huntly BJ, Delabesse E, Fourouclas N, Hunt AR, Deloukas P, Green AR. Bench AJ, et al. Among authors: li j. Br J Haematol. 2004 Dec;127(5):509-18. doi: 10.1111/j.1365-2141.2004.05278.x. Br J Haematol. 2004. PMID: 15566354 Free article.

6

L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting.

Li J, Bench AJ, Piltz S, Vassiliou G, Baxter EJ, Ferguson-Smith AC, Green AR. Li J, et al. Genomics. 2005 Oct;86(4):489-94. doi: 10.1016/j.ygeno.2005.06.012. Genomics. 2005. PMID: 16081246

7

An acquired translocation in JAK2 Val617Phe-negative essential thrombocythemia associated with autosomal spread of X-inactivation.

Vassiliou GS, Campbell PJ, Li J, Roberts I, Swanton S, Huntly BJ, Fourouclas N, Baxter EJ, Munro LR, Culligan DA, Scott LM, Green AR. Vassiliou GS, et al. Among authors: li j. Haematologica. 2006 Aug;91(8):1100-4. Haematologica. 2006. PMID: 16885051

8

Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders.

Fourouclas N, Li J, Gilby DC, Campbell PJ, Beer PA, Boyd EM, Goodeve AC, Bareford D, Harrison CN, Reilly JT, Green AR, Bench AJ. Fourouclas N, et al. Among authors: li j. Haematologica. 2008 Nov;93(11):1635-44. doi: 10.3324/haematol.13043. Epub 2008 Sep 24. Haematologica. 2008. PMID: 18815196 Free article.

9

JAK2 V617F impairs hematopoietic stem cell function in a conditional knock-in mouse model of JAK2 V617F-positive essential thrombocythemia.

Li J, Spensberger D, Ahn JS, Anand S, Beer PA, Ghevaert C, Chen E, Forrai A, Scott LM, Ferreira R, Campbell PJ, Watson SP, Liu P, Erber WN, Huntly BJ, Ottersbach K, Green AR. Li J, et al. Blood. 2010 Sep 2;116(9):1528-38. doi: 10.1182/blood-2009-12-259747. Epub 2010 May 20. Blood. 2010. PMID: 20489053 Free PMC article.

10

cis-Regulatory remodeling of the SCL locus during vertebrate evolution.

Göttgens B, Ferreira R, Sanchez MJ, Ishibashi S, Li J, Spensberger D, Lefevre P, Ottersbach K, Chapman M, Kinston S, Knezevic K, Hoogenkamp M, Follows GA, Bonifer C, Amaya E, Green AR. Göttgens B, et al. Among authors: li j. Mol Cell Biol. 2010 Dec;30(24):5741-51. doi: 10.1128/MCB.00870-10. Epub 2010 Oct 18. Mol Cell Biol. 2010. PMID: 20956563 Free PMC article.

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