Jennings CE - Search Results

1

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH. Velaga MR, et al. Among authors: jennings ce. J Clin Endocrinol Metab. 2004 Nov;89(11):5862-5. doi: 10.1210/jc.2004-1108. J Clin Endocrinol Metab. 2004. PMID: 15531553

2

Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.

Owen CJ, Jennings CE, Imrie H, Lachaux A, Bridges NA, Cheetham TD, Pearce SH. Owen CJ, et al. Among authors: jennings ce. J Clin Endocrinol Metab. 2003 Dec;88(12):6034-9. doi: 10.1210/jc.2003-031080. J Clin Endocrinol Metab. 2003. PMID: 14671208

3

Role of the CD40 locus in Graves' disease.

Houston FA, Wilson V, Jennings CE, Owen CJ, Donaldson P, Perros P, Pearce SH. Houston FA, et al. Among authors: jennings ce. Thyroid. 2004 Jul;14(7):506-9. doi: 10.1089/1050725041517039. Thyroid. 2004. PMID: 15307939

4

No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease.

Jennings CE, Owen CJ, Wilson V, Pearce SH. Jennings CE, et al. Clin Endocrinol (Oxf). 2005 Mar;62(3):362-5. doi: 10.1111/j.1365-2265.2005.02224.x. Clin Endocrinol (Oxf). 2005. PMID: 15730420

5

A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population.

Jennings CE, Owen CJ, Wilson V, Pearce SH. Jennings CE, et al. J Mol Endocrinol. 2005 Jun;34(3):859-63. doi: 10.1677/jme.1.01760. J Mol Endocrinol. 2005. PMID: 15956353

6

Macroorchidism in two unrelated prepubertal boys with a normal FSH receptor.

Velaga MR, Wright C, Crofton PM, Allen L, Jennings CE, Cheetham TD. Velaga MR, et al. Among authors: jennings ce. Horm Res. 2005;64(1):3-8. doi: 10.1159/000087287. Epub 2005 Aug 2. Horm Res. 2005. PMID: 16088201

7

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.

Owen CJ, Eden JA, Jennings CE, Wilson V, Cheetham TD, Pearce SH. Owen CJ, et al. Among authors: jennings ce. J Mol Endocrinol. 2006 Aug;37(1):97-104. doi: 10.1677/jme.1.02072. J Mol Endocrinol. 2006. PMID: 16901927

8

The deleted in colorectal carcinoma (DCC) gene 201 R --> G polymorphism: no evidence for genetic association with autoimmune disease.

Hall RJ, Merriman ME, Green RA, Markham VH, Smyth DJ, Heward JM, Jennings CE, Braithwaite AW, Cundy T, Darlow BA, Gow PJ, Harrison AA, Highton J, Hunt PJ, Manning P, Pokorny V, Scott RS, Taylor BJ, Willis JA, Yeoman S, McLean L, Gough SC, Pearce SH, Merriman TR. Hall RJ, et al. Among authors: jennings ce. Eur J Hum Genet. 2003 Nov;11(11):840-4. doi: 10.1038/sj.ejhg.5201059. Eur J Hum Genet. 2003. PMID: 14571268

9

Identification of a novel ligand for the ATAD2 bromodomain with selectivity over BRD4 through a fragment growing approach.

Miller DC, Martin MP, Adhikari S, Brennan A, Endicott JA, Golding BT, Hardcastle IR, Heptinstall A, Hobson S, Jennings C, Molyneux L, Ng Y, Wedge SR, Noble MEM, Cano C. Miller DC, et al. Org Biomol Chem. 2018 Mar 14;16(11):1843-1850. doi: 10.1039/c8ob00099a. Org Biomol Chem. 2018. PMID: 29469144 Free PMC article.

10

Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein-Protein Interaction.

Chessari G, Hardcastle IR, Ahn JS, Anil B, Anscombe E, Bawn RH, Bevan LD, Blackburn TJ, Buck I, Cano C, Carbain B, Castro J, Cons B, Cully SJ, Endicott JA, Fazal L, Golding BT, Griffin RJ, Haggerty K, Harnor SJ, Hearn K, Hobson S, Holvey RS, Howard S, Jennings CE, Johnson CN, Lunec J, Miller DC, Newell DR, Noble MEM, Reeks J, Revill CH, Riedinger C, St Denis JD, Tamanini E, Thomas H, Thompson NT, Vinković M, Wedge SR, Williams PA, Wilsher NE, Zhang B, Zhao Y. Chessari G, et al. Among authors: jennings ce. J Med Chem. 2021 Apr 8;64(7):4071-4088. doi: 10.1021/acs.jmedchem.0c02188. Epub 2021 Mar 24. J Med Chem. 2021. PMID: 33761253

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