219 related articles for article (PubMed ID: 16411201)
1. Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome.
Matsuura S; Matsumoto Y; Morishima K; Izumi H; Matsumoto H; Ito E; Tsutsui K; Kobayashi J; Tauchi H; Kajiwara Y; Hama S; Kurisu K; Tahara H; Oshimura M; Komatsu K; Ikeuchi T; Kajii T
Am J Med Genet A; 2006 Feb; 140(4):358-67. PubMed ID: 16411201
[TBL] [Abstract][Full Text] [Related]
2. Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B.
Hanks S; Coleman K; Reid S; Plaja A; Firth H; Fitzpatrick D; Kidd A; Méhes K; Nash R; Robin N; Shannon N; Tolmie J; Swansbury J; Irrthum A; Douglas J; Rahman N
Nat Genet; 2004 Nov; 36(11):1159-61. PubMed ID: 15475955
[TBL] [Abstract][Full Text] [Related]
3. Chromosomal instability syndrome of total premature chromatid separation with mosaic variegated aneuploidy is defective in mitotic-spindle checkpoint.
Matsuura S; Ito E; Tauchi H; Komatsu K; Ikeuchi T; Kajii T
Am J Hum Genet; 2000 Aug; 67(2):483-6. PubMed ID: 10877982
[TBL] [Abstract][Full Text] [Related]
4. Gradual reduction of BUBR1 protein levels results in premature sister-chromatid separation then in aneuploidy.
Bohers E; Sarafan-Vasseur N; Drouet A; Paresy M; Latouche JB; Flaman JM; Sesboüé R; Frebourg T
Hum Genet; 2008 Dec; 124(5):473-8. PubMed ID: 18932004
[TBL] [Abstract][Full Text] [Related]
5. TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.
Ochiai H; Miyamoto T; Kanai A; Hosoba K; Sakuma T; Kudo Y; Asami K; Ogawa A; Watanabe A; Kajii T; Yamamoto T; Matsuura S
Proc Natl Acad Sci U S A; 2014 Jan; 111(4):1461-6. PubMed ID: 24344301
[TBL] [Abstract][Full Text] [Related]
6. Clinical and genetic heterogeneity in patients with mosaic variegated aneuploidy: delineation of clinical subtypes.
García-Castillo H; Vásquez-Velásquez AI; Rivera H; Barros-Núñez P
Am J Med Genet A; 2008 Jul; 146A(13):1687-95. PubMed ID: 18548531
[TBL] [Abstract][Full Text] [Related]
7. Nearly complete deletion of BubR1 causes microcephaly through shortened mitosis and massive cell death.
Simmons AJ; Park R; Sterling NA; Jang MH; van Deursen JMA; Yen TJ; Cho SH; Kim S
Hum Mol Genet; 2019 Jun; 28(11):1822-1836. PubMed ID: 30668728
[TBL] [Abstract][Full Text] [Related]
8. Molecular causes for BUBR1 dysfunction in the human cancer predisposition syndrome mosaic variegated aneuploidy.
Suijkerbuijk SJ; van Osch MH; Bos FL; Hanks S; Rahman N; Kops GJ
Cancer Res; 2010 Jun; 70(12):4891-900. PubMed ID: 20516114
[TBL] [Abstract][Full Text] [Related]
9. BubR1 is essential for kinetochore localization of other spindle checkpoint proteins and its phosphorylation requires Mad1.
Chen RH
J Cell Biol; 2002 Aug; 158(3):487-96. PubMed ID: 12163471
[TBL] [Abstract][Full Text] [Related]
10. Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome.
Pavone P; Pappalardo XG; Mustafa N; Falsaperla R; Marino SD; Corsello G; Bianca S; Parano E; Ruggieri M
Neurol Sci; 2022 Nov; 43(11):6529-6538. PubMed ID: 35804254
[TBL] [Abstract][Full Text] [Related]
11. BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.
Izumi H; Matsumoto Y; Ikeuchi T; Saya H; Kajii T; Matsuura S
Oncogene; 2009 Aug; 28(31):2806-20. PubMed ID: 19503101
[TBL] [Abstract][Full Text] [Related]
12. Bub1 and aurora B cooperate to maintain BubR1-mediated inhibition of APC/CCdc20.
Morrow CJ; Tighe A; Johnson VL; Scott MI; Ditchfield C; Taylor SS
J Cell Sci; 2005 Aug; 118(Pt 16):3639-52. PubMed ID: 16046481
[TBL] [Abstract][Full Text] [Related]
13. Mosaic variegated aneuploidy with multiple congenital abnormalities: homozygosity for total premature chromatid separation trait.
Kajii T; Kawai T; Takumi T; Misu H; Mabuchi O; Takahashi Y; Tachino M; Nihei F; Ikeuchi T
Am J Med Genet; 1998 Jul; 78(3):245-9. PubMed ID: 9677059
[TBL] [Abstract][Full Text] [Related]
14. Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.
Miyamoto T; Porazinski S; Wang H; Borovina A; Ciruna B; Shimizu A; Kajii T; Kikuchi A; Furutani-Seiki M; Matsuura S
Hum Mol Genet; 2011 May; 20(10):2058-70. PubMed ID: 21389084
[TBL] [Abstract][Full Text] [Related]
15. p55CDC/hCDC20 is associated with BUBR1 and may be a downstream target of the spindle checkpoint kinase.
Wu H; Lan Z; Li W; Wu S; Weinstein J; Sakamoto KM; Dai W
Oncogene; 2000 Sep; 19(40):4557-62. PubMed ID: 11030144
[TBL] [Abstract][Full Text] [Related]
16. Prevalence of germline mutations in the spindle assembly checkpoint gene BUB1B in individuals with early-onset colorectal cancer.
Hahn MM; Vreede L; Bemelmans SA; van der Looij E; van Kessel AG; Schackert HK; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; de Voer RM
Genes Chromosomes Cancer; 2016 Nov; 55(11):855-63. PubMed ID: 27239782
[TBL] [Abstract][Full Text] [Related]
17. Comparative genomic hybridization and BUB1B mutation analyses in childhood cancers associated with mosaic variegated aneuploidy syndrome.
Hanks S; Coleman K; Summersgill B; Messahel B; Williamson D; Pritchard-Jones K; Strefford J; Swansbury J; Plaja A; Shipley J; Rahman N
Cancer Lett; 2006 Aug; 239(2):234-8. PubMed ID: 16182441
[TBL] [Abstract][Full Text] [Related]
18. Uncoupling of the spindle-checkpoint and chromosome-congression functions of BubR1.
Elowe S; Dulla K; Uldschmid A; Li X; Dou Z; Nigg EA
J Cell Sci; 2010 Jan; 123(Pt 1):84-94. PubMed ID: 20016069
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of premature chromatid separation/mosaic variegated aneuploidy (PCS/MVA) syndrome.
Yamaguchi T; Yamaguchi M; Akeno K; Fujisaki M; Sumiyoshi K; Ohashi M; Sameshima H; Ozaki M; Kato M; Kato T; Hosoba E; Kurahashi H
J Obstet Gynaecol Res; 2018 Jul; 44(7):1313-1317. PubMed ID: 29673003
[TBL] [Abstract][Full Text] [Related]
20. Checkpoint protein BubR1 acts synergistically with Mad2 to inhibit anaphase-promoting complex.
Fang G
Mol Biol Cell; 2002 Mar; 13(3):755-66. PubMed ID: 11907259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
