Poole JC - Search Results

1

p21Waf1/Cip1/Sdi1-induced growth arrest is associated with depletion of mitosis-control proteins and leads to abnormal mitosis and endoreduplication in recovering cells.

Chang BD, Broude EV, Fang J, Kalinichenko TV, Abdryashitov R, Poole JC, Roninson IB. Chang BD, et al. Among authors: poole jc. Oncogene. 2000 Apr 20;19(17):2165-70. doi: 10.1038/sj.onc.1203573. Oncogene. 2000. PMID: 10815808

2

Induction of transcription by p21Waf1/Cip1/Sdi1: role of NFkappaB and effect of non-steroidal anti-inflammatory drugs.

Poole JC, Thain A, Perkins ND, Roninson IB. Poole JC, et al. Cell Cycle. 2004 Jul;3(7):931-40. Epub 2004 Jul 13. Cell Cycle. 2004. PMID: 15190207

3

Effects of p21Waf1/Cip1/Sdi1 on cellular gene expression: implications for carcinogenesis, senescence, and age-related diseases.

Chang BD, Watanabe K, Broude EV, Fang J, Poole JC, Kalinichenko TV, Roninson IB. Chang BD, et al. Among authors: poole jc. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4291-6. doi: 10.1073/pnas.97.8.4291. Proc Natl Acad Sci U S A. 2000. PMID: 10760295 Free PMC article.

4

Induction of transcription through the p300 CRD1 motif by p21WAF1/CIP1 is core promoter specific and cyclin dependent kinase independent.

Gregory DJ, Garcia-Wilson E, Poole JC, Snowden AW, Roninson IB, Perkins ND. Gregory DJ, et al. Among authors: poole jc. Cell Cycle. 2002 Sep-Oct;1(5):343-50. Cell Cycle. 2002. PMID: 12461297

5

Three new members of the mouse prolactin/growth hormone family are homologous to proteins expressed in the rat.

Lin J, Poole J, Linzer DI. Lin J, et al. Endocrinology. 1997 Dec;138(12):5541-9. doi: 10.1210/endo.138.12.5626. Endocrinology. 1997. PMID: 9389542

6

Two novel members of the prolactin/growth hormone family are expressed in the mouse placenta.

Lin J, Poole J, Linzer DI. Lin J, et al. Endocrinology. 1997 Dec;138(12):5535-40. doi: 10.1210/endo.138.12.5636. Endocrinology. 1997. PMID: 9389541

7

Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants.

Poole JC, Procaccio V, Brandon MC, Merrick G, Wallace DC. Poole JC, et al. Biol Chem. 2010 Oct;391(10):1115-30. doi: 10.1515/BC.2010.125. Biol Chem. 2010. PMID: 20707610 Free PMC article.

8

An enhanced MITOMAP with a global mtDNA mutational phylogeny.

Ruiz-Pesini E, Lott MT, Procaccio V, Poole JC, Brandon MC, Mishmar D, Yi C, Kreuziger J, Baldi P, Wallace DC. Ruiz-Pesini E, et al. Among authors: poole jc. Nucleic Acids Res. 2007 Jan;35(Database issue):D823-8. doi: 10.1093/nar/gkl927. Epub 2006 Dec 18. Nucleic Acids Res. 2007. PMID: 17178747 Free PMC article.

9

Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy.

Bannwarth S, Procaccio V, Rouzier C, Fragaki K, Poole J, Chabrol B, Desnuelle C, Pouget J, Azulay JP, Attarian S, Pellissier JF, Gargus JJ, Abdenur JE, Mozaffar T, Calvas P, Labauge P, Pages M, Wallace DC, Lambert JC, Paquis-Flucklinger V. Bannwarth S, et al. Among authors: poole j. Mitochondrion. 2008 Mar;8(2):136-45. doi: 10.1016/j.mito.2007.10.008. Epub 2007 Nov 6. Mitochondrion. 2008. PMID: 18078792

10

Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.

Procaccio V, Neckelmann N, Paquis-Flucklinger V, Bannwarth S, Jimenez R, Davila A, Poole JC, Wallace DC. Procaccio V, et al. Among authors: poole jc. Mol Diagn Ther. 2006;10(6):381-9. doi: 10.1007/BF03256215. Mol Diagn Ther. 2006. PMID: 17154655

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