KLHDC8B in Hodgkin lymphoma and possibly twinning

References

• Kuppers R. The biology of Hodgkin’s lymphoma. Nat Rev Cancer 2009; 9:15 - 27
   PubMed Web of Science ®Google Scholar
• Altieri A, Hemminki K. The familial risk of Hodgkin’s lymphoma ranks among the highest in the Swedish Family-Cancer Database. Leukemia 2006; 20:2062 - 2063
   PubMed Web of Science ®Google Scholar
• Diepstra A, Niens M, te Meerman GJ, Poppema S, van den Berg A. Genetic susceptibility to Hodgkin’s lymphoma associated with the human leukocyte antigen region. Eur J Haematol Suppl 2005; 34 - 41
   PubMedGoogle Scholar
• Rieux-Laucat F, Le Deist F, Fischer A. Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways. Cell Death Differ 2003; 10:124 - 133
   PubMed Web of Science ®Google Scholar
• Horwitz M, Wiernik PH. Pseudoautosomal linkage of Hodgkin disease. Am J Hum Genet 1999; 65:1413 - 1422
   PubMed Web of Science ®Google Scholar
• Horwitz MS, Mealiffe ME. Further evidence for a pseudoautosomal gene for Hodgkin’s lymphoma: Reply to ‘The familial risk of Hodgkin’s lymphoma ranks among the highest in the Swedish Family- Cancer Database’ by Altieri A and Hemminki K. Leukemia 2 2007; 21:351
   PubMed Web of Science ®Google Scholar
• Grufferman S, Cole P, Smith PG, Lukes RJ. Hodgkin’s disease in siblings. N Engl J Med 1977; 296:248 - 250
   PubMed Web of Science ®Google Scholar
• Anderson D. Sports of the Times; on being Mickey Mantle. New York Times. New York 1994; 11
   Google Scholar
• Gokhale DA, Evans DG, Crowther D, Woll P, Watson CJ, Dearden SP, et al. Molecular genetic analysis of a family with a history of Hodgkin’s disease and dyschondrosteosis. Leukemia 1995; 9:826 - 833
   PubMed Web of Science ®Google Scholar
• Shears DJ, Endris V, Gokhale DA, Dearden SP, Radford JA, Rappold GA, Taylor GM. Pseudoautosomal linkage of familial Hodgkin’s lymphoma: molecular analysis of a unique family with Leri-Weill dyschondrosteosis and Hodgkins lymphoma. Br J Haematol 2003; 121:377 - 379
   PubMed Web of Science ®Google Scholar
• Salipante SJ, Mealiffe ME, Wechsler J, Krem MM, Liu Y, Namkoong S. Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cells. Proc Natl Acad Sci USA 2009; 106:14920 - 14925
   PubMed Web of Science ®Google Scholar
• Szeles A. Fluorescence in situ hybridization (FISH) in the molecular cytogenetics of cancer. Acta Microbiol Immunol Hung 2002; 49:69 - 80
   PubMedGoogle Scholar
• Yang Q, Yoshimura G, Mori I, Sakurai T, Kakudo K. Chromosome 3p and breast cancer. J Hum Genet 2002; 47:453 - 459
   PubMed Web of Science ®Google Scholar
• Hesson LB, Cooper WN, Latif F. Evaluation of the 3p21.3 tumour-suppressor gene cluster. Oncogene 2007; 26:7283 - 7301
   PubMed Web of Science ®Google Scholar
• Xiong W, Zeng ZY, Xia JH, Xia K, Shen SR, Li XL, et al. A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma. Cancer Res 2004; 64:1972 - 1974
   PubMed Web of Science ®Google Scholar
• Cheng Y, Poulos NE, Lung ML, Hampton G, Ou B, Lerman MI, Stanbridge EJ. Functional evidence for a nasopharyngeal carcinoma tumor suppressor gene that maps at chromosome 3p21.3. Proc Natl Acad Sci USA 1998; 95:3042 - 3047
   PubMed Web of Science ®Google Scholar
• Chan AS, To KF, Lo KW, Mak KF, Pak W, Chiu B, et al. High frequency of chromosome 3p deletion in histologically normal nasopharyngeal epithelia from Southern Chinese. Cancer Res 2000; 60:5365 - 5370
   PubMed Web of Science ®Google Scholar
• Kutok JL, Wang F. Spectrum of Epstein-Barr virus-associated diseases. Annu Rev Pathol 2006; 1:375 - 404
   PubMed Web of Science ®Google Scholar
• Prag S, Adams JC. Molecular phylogeny of the kelch-repeat superfamily reveals an expansion of BTB/kelch proteins in animals. BMC Bioinformatics 2003; 4:42
   PubMed Web of Science ®Google Scholar
• Xue F, Cooley L. kelch encodes a component of intercellular bridges in Drosophila egg chambers. Cell 1993; 72:681 - 693
   PubMed Web of Science ®Google Scholar
• Sumara I, Quadroni M, Frei C, Olma MH, Sumara G, Ricci R, Peter M. A Cul3-based E3 ligase removes Aurora B from mitotic chromosomes, regulating mitotic progression and completion of cytokinesis in human cells. Dev Cell 2007; 12:887 - 900
   PubMed Web of Science ®Google Scholar
• Pepling ME, Spradling AC. Mouse ovarian germ cell cysts undergo programmed breakdown to form primordial follicles. Dev Biol 2001; 234:339 - 351
   PubMed Web of Science ®Google Scholar
• Derom C, Jawaheer D, Chen WV, McBride KL, Xiao X, Amos C. Genome-wide linkage scan for spontaneous DZ twinning. Eur J Hum Genet 2006; 14:117 - 122
   PubMed Web of Science ®Google Scholar
• Hemminki K, Li X. Cancer risks in twins: results from the Swedish family-cancer database. Int J Cancer 2002; 99:873 - 878
   PubMed Web of Science ®Google Scholar
• Bieber FR, Nance WE, Morton CC, Brown JA, Redwine FO, Jordan RL, Mohanakumar T. Genetic studies of an acardiac monster: evidence of polar body twinning in man. Science 1981; 213:775 - 777
   PubMed Web of Science ®Google Scholar
• Goldgar DE, Kimberling WJ. Genetic expectations of polar body twinning. Acta Genet Med Gemellol (Roma) 1981; 30:257 - 266
   PubMed Web of Science ®Google Scholar
• Elston RC, Boklage CE. An examination of fundamental assumptions of the twin method. Prog Clin Biol Res 1978; 24:189 - 199
   PubMedGoogle Scholar
• Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81:559 - 575
   PubMed Web of Science ®Google Scholar
• Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30:97 - 101
   PubMed Web of Science ®Google Scholar
• Albrechtsen A, Sand Korneliussen T, Moltke I, van Overseem Hansen T, Nielsen FC, Nielsen R. Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. Genet Epidemiol 2009; 33:266 - 274
   PubMed Web of Science ®Google Scholar