| Year |
Citation |
Score |
| 2012 |
Stanbery L, Petty EM. Steps solidifying a role for SEPT9 in breast cancer suggest that greater strides are needed. Breast Cancer Research : Bcr. 14: 101. PMID 22236777 DOI: 10.1186/bcr3056 |
0.311 |
|
| 2011 |
Peterson EA, Stanbery L, Li C, Kocak H, Makarova O, Petty EM. SEPT9_i1 and genomic instability: mechanistic insights and relevance to tumorigenesis. Genes, Chromosomes & Cancer. 50: 940-9. PMID 21910160 DOI: 10.1002/Gcc.20916 |
0.78 |
|
| 2011 |
Keller JA, Petty EM. CHFR binds to and regulates MAD2 in the spindle checkpoint through its cysteine-rich domain. Biochemical and Biophysical Research Communications. 409: 389-93. PMID 21575600 DOI: 10.1016/J.Bbrc.2011.04.143 |
0.328 |
|
| 2011 |
Marvin ML, Mazzoni SM, Herron CM, Edwards S, Gruber SB, Petty EM. AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. American Journal of Medical Genetics. Part A. 155: 898-902. PMID 21416598 DOI: 10.1002/Ajmg.A.33927 |
0.31 |
|
| 2011 |
Erson AE, Petty EM. Kidney: Nephroblastoma (Wilms tumor) Atlas of Genetics and Cytogenetics in Oncology and Haematology. DOI: 10.4267/2042/38390 |
0.754 |
|
| 2011 |
Erson AE, Petty EM. TRIM37 (tripartite motif-containing 37) Atlas of Genetics and Cytogenetics in Oncology and Haematology. DOI: 10.4267/2042/38349 |
0.754 |
|
| 2010 |
Keller JA, Erson-Bensan AE, Petty EM. Connections between CHFR, the cell cycle, and chemosensitivity: Are they critical in cancer? Cancer Biology & Therapy. 10: 942-4. PMID 21057211 DOI: 10.4161/Cbt.10.9.13876 |
0.352 |
|
| 2010 |
Stanbery L, D'Silva NJ, Lee JS, Bradford CR, Carey TE, Prince ME, Wolf GT, Worden FP, Cordell KG, Petty EM. High SEPT9_v1 Expression Is Associated with Poor Clinical Outcomes in Head and Neck Squamous Cell Carcinoma. Translational Oncology. 3: 239-45. PMID 20689765 DOI: 10.1593/Tlo.10109 |
0.33 |
|
| 2010 |
Akhavantabasi S, Akman HB, Sapmaz A, Keller J, Petty EM, Erson AE. USP32 is an active, membrane-bound ubiquitin protease overexpressed in breast cancers. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 388-97. PMID 20549504 DOI: 10.1007/S00335-010-9268-4 |
0.81 |
|
| 2010 |
Peterson EA, Petty EM. Conquering the complex world of human septins: implications for health and disease. Clinical Genetics. 77: 511-24. PMID 20236126 DOI: 10.1111/J.1399-0004.2010.01392.X |
0.773 |
|
| 2009 |
Erson AE, Petty EM. miRNAs and cancer: New research developments and potential clinical applications. Cancer Biology & Therapy. 8: 2317-22. PMID 20168083 DOI: 10.4161/Cbt.8.24.10765 |
0.768 |
|
| 2009 |
Landsverk ML, Ruzzo EK, Mefford HC, Buysse K, Buchan JG, Eichler EE, Petty EM, Peterson EA, Knutzen DM, Barnett K, Farlow MR, Caress J, Parry GJ, Quan D, Gardner KL, et al. Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Human Molecular Genetics. 18: 1200-8. PMID 19139049 DOI: 10.1093/Hmg/Ddp014 |
0.728 |
|
| 2009 |
Gonzalez ME, Makarova O, Peterson EA, Privette LM, Petty EM. Up-regulation of SEPT9_v1 stabilizes c-Jun-N-terminal kinase and contributes to its pro-proliferative activity in mammary epithelial cells. Cellular Signalling. 21: 477-87. PMID 19071215 DOI: 10.1016/J.Cellsig.2008.11.007 |
0.759 |
|
| 2008 |
Erson AE, Petty EM. MicroRNAs in development and disease. Clinical Genetics. 74: 296-306. PMID 18713256 DOI: 10.1111/J.1399-0004.2008.01076.X |
0.755 |
|
| 2008 |
Privette LM, Petty EM. CHFR: A Novel Mitotic Checkpoint Protein and Regulator of Tumorigenesis. Translational Oncology. 1: 57-64. PMID 18633460 DOI: 10.1593/Tlo.08109 |
0.778 |
|
| 2008 |
Privette LM, Weier JF, Nguyen HN, Yu X, Petty EM. Loss of CHFR in human mammary epithelial cells causes genomic instability by disrupting the mitotic spindle assembly checkpoint. Neoplasia (New York, N.Y.). 10: 643-52. PMID 18592005 DOI: 10.1593/Neo.08176 |
0.776 |
|
| 2008 |
Roth TM, Petty EM, Barald KF. The role of steroid hormones in the NF1 phenotype: focus on pregnancy. American Journal of Medical Genetics. Part A. 146: 1624-33. PMID 18481270 DOI: 10.1002/Ajmg.A.32301 |
0.347 |
|
| 2007 |
Sharma MR, Petty EM, Lesperance MM. Airway obstruction caused by PTEN hamartoma (Bannayan-Riley-Ruvalcaba) syndrome. Archives of Otolaryngology--Head & Neck Surgery. 133: 1157-60. PMID 18025323 DOI: 10.1001/Archotol.133.11.1157 |
0.331 |
|
| 2007 |
Peterson EA, Kalikin LM, Steels JD, Estey MP, Trimble WS, Petty EM. Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 796-807. PMID 17922164 DOI: 10.1007/S00335-007-9065-X |
0.78 |
|
| 2007 |
Gonzalez ME, Peterson EA, Privette LM, Loffreda-Wren JL, Kalikin LM, Petty EM. High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes. Cancer Research. 67: 8554-64. PMID 17875694 DOI: 10.1158/0008-5472.Can-07-1474 |
0.757 |
|
| 2007 |
Privette LM, González ME, Ding L, Kleer CG, Petty EM. Altered expression of the early mitotic checkpoint protein, CHFR, in breast cancers: implications for tumor suppression. Cancer Research. 67: 6064-74. PMID 17596595 DOI: 10.1158/0008-5472.Can-06-4109 |
0.795 |
|
| 2007 |
Chao MM, Levine JE, Ruiz RE, Kohlmann WK, Bower MA, Petty EM, Mody RJ. Malignant triton tumor in a patient with Li-Fraumeni syndrome and a novel TP53 mutation Pediatric Blood and Cancer. 49: 1000-1004. PMID 16333835 DOI: 10.1002/Pbc.20700 |
0.315 |
|
| 2004 |
Erson AE, Petty EM. CHFR-associated early G2/M checkpoint defects in breast cancer cells. Molecular Carcinogenesis. 39: 26-33. PMID 14694445 DOI: 10.1002/Mc.10161 |
0.813 |
|
| 2002 |
Macara IG, Baldarelli R, Field CM, Glotzer M, Hayashi Y, Hsu SC, Kennedy MB, Kinoshita M, Longtine M, Low C, Maltais LJ, McKenzie L, Mitchison TJ, Nishikawa T, Noda M, ... Petty EM, et al. Mammalian septins nomenclature. Molecular Biology of the Cell. 13: 4111-3. PMID 12475938 DOI: 10.1091/Mbc.E02-07-0438 |
0.347 |
|
| 2002 |
Rosenberg MJ, Agarwala R, Bouffard G, Davis J, Fiermonte G, Hilliard MS, Koch T, Kalikin LM, Makalowska I, Morton DH, Petty EM, Weber JL, Palmieri F, Kelley RI, Schäffer AA, et al. Mutant deoxynucleotide carrier is associated with congenital microcephaly. Nature Genetics. 32: 175-9. PMID 12185364 DOI: 10.1038/Ng948 |
0.333 |
|
| 2002 |
Boerkoel CF, Takashima H, John J, Yan J, Stankiewicz P, Rosenbarker L, André JL, Bogdanovic R, Burguet A, Cockfield S, Cordeiro I, Fründ S, Illies F, Joseph M, Kaitila I, ... ... Petty EM, et al. Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia. Nature Genetics. 30: 215-20. PMID 11799392 DOI: 10.1038/Ng821 |
0.306 |
|
| 2002 |
Kalikin LM, Bugeaud EM, Palmbos PL, Lyons RH, Petty EM. Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 925-9. PMID 11707779 DOI: 10.1007/S00335-001-2073-3 |
0.456 |
|
| 2001 |
Erson AE, Niell BL, DeMers SK, Rouillard JM, Hanash SM, Petty EM. Overexpressed genes/ESTs and characterization of distinct amplicons on 17q23 in breast cancer cells Neoplasia. 3: 521-526. PMID 11774034 DOI: 10.1038/Sj.Neo.7900187 |
0.797 |
|
| 2001 |
Rouillard JM, Erson AE, Kuick R, Asakawa J, Wimmer K, Muleris M, Petty EM, Hanash S. Virtual genome scan: a tool for restriction landmark-based scanning of the human genome. Genome Research. 11: 1453-9. PMID 11483587 DOI: 10.1101/Gr.181601 |
0.76 |
|
| 2001 |
Percy MJ, Myrie KA, Neeley CK, Azim JN, Ethier SP, Petty EM. Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells. Genes, Chromosomes & Cancer. 29: 356-62. PMID 11066082 DOI: 10.1002/1098-2264(2000)9999:9999<::Aid-Gcc1044>3.0.Co;2-N |
0.527 |
|
| 2000 |
Myrie KA, Percy MJ, Azim JN, Neeley CK, Petty EM. Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines. Cancer Letters. 152: 193-9. PMID 10773412 DOI: 10.1016/S0304-3835(00)00340-2 |
0.516 |
|
| 2000 |
Kalikin LM, Sims HL, Petty EM. Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors. Genomics. 63: 165-72. PMID 10673329 DOI: 10.1006/Geno.1999.6077 |
0.461 |
|
| 1999 |
Kalikin LM, George RA, Keller MP, Bort S, Bowler NS, Law DJ, Chance PF, Petty EM. An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci. Genomics. 57: 36-42. PMID 10191081 DOI: 10.1006/Geno.1998.5740 |
0.363 |
|
| 1998 |
Petty EM, Kalikin LM, Orringer MB, Beer DG. Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: implications for tumorigenesis. Molecular Carcinogenesis. 22: 222-8. PMID 9726814 DOI: 10.1002/(Sici)1098-2744(199808)22:4<222::Aid-Mc3>3.0.Co;2-L |
0.339 |
|
| 1997 |
Kalikin LM, Frank TS, Svoboda-Newman SM, Wetzel JC, Cooney KA, Petty EM. A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors. Oncogene. 14: 1991-4. PMID 9150366 DOI: 10.1038/Sj.Onc.1201013 |
0.391 |
|
| 1997 |
Petty EM, Killeen AA. BRCA1 Mutation Testing: Controversies and Challenges Clinical Chemistry. 43: 6-8. DOI: 10.1093/Clinchem/43.1.6 |
0.414 |
|
| 1997 |
Petty EM. Cellular cancer markers American Journal of Medical Genetics. 68: 492-493. DOI: 10.1002/(Sici)1096-8628(19970211)68:4<492::Aid-Ajmg29>3.0.Co;2-M |
0.344 |
|
| 1996 |
Kalikin LM, Qu X, Frank TS, Caduff RF, Svoboda SM, Law DJ, Petty EM. Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25. Genes, Chromosomes & Cancer. 17: 64-8. PMID 8889509 DOI: 10.1002/(Sici)1098-2264(199609)17:1<64::Aid-Gcc10>3.0.Co;2-H |
0.441 |
|
| 1996 |
Merajver SD, Petty EM. Risk assessment and presymptomatic molecular diagnosis in hereditary breast cancer Clinics in Laboratory Medicine. 16: 139-167. PMID 8867588 DOI: 10.1016/S0272-2712(18)30292-0 |
0.412 |
|
| 1996 |
Petty EM, Miller DE, Grant AL, Collins EE, Glover TW, Law DJ. FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors. Cytogenetics and Cell Genetics. 72: 319-21. PMID 8641139 DOI: 10.1159/000134213 |
0.458 |
|
| 1995 |
Law DJ, Prasad MA, King SE, Spranger KD, Lee YH, Fox RE, Collins EE, Gebuhr TC, Miller DE, Petty EM. Localization of the human estrogen-responsive finger protein (EEP) gene (ZNF147) within a YAC contig containing the myeloperoxidase (MPO) gene. Genomics. 28: 361-3. PMID 8530055 DOI: 10.1006/Geno.1995.1160 |
0.451 |
|
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