270 related articles for article (PubMed ID: 35701783)
1. Mechanisms of structural chromosomal rearrangement formation.
Burssed B; Zamariolli M; Bellucco FT; Melaragno MI
Mol Cytogenet; 2022 Jun; 15(1):23. PubMed ID: 35701783
[TBL] [Abstract][Full Text] [Related]
2. FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.
Koumbaris G; Hatzisevastou-Loukidou H; Alexandrou A; Ioannides M; Christodoulou C; Fitzgerald T; Rajan D; Clayton S; Kitsiou-Tzeli S; Vermeesch JR; Skordis N; Antoniou P; Kurg A; Georgiou I; Carter NP; Patsalis PC
Hum Mol Genet; 2011 May; 20(10):1925-36. PubMed ID: 21349920
[TBL] [Abstract][Full Text] [Related]
3. Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
Verdin H; D'haene B; Beysen D; Novikova Y; Menten B; Sante T; Lapunzina P; Nevado J; Carvalho CM; Lupski JR; De Baere E
PLoS Genet; 2013; 9(3):e1003358. PubMed ID: 23516377
[TBL] [Abstract][Full Text] [Related]
4. Decoding NF1 Intragenic Copy-Number Variations.
Hsiao MC; Piotrowski A; Callens T; Fu C; Wimmer K; Claes KB; Messiaen L
Am J Hum Genet; 2015 Aug; 97(2):238-49. PubMed ID: 26189818
[TBL] [Abstract][Full Text] [Related]
5. Aberrant X chromosomal rearrangement through multi-step template switching during sister chromatid formation in a patient with severe hemophilia A.
Tokoro M; Tamura S; Suzuki N; Kakihara M; Hattori Y; Odaira K; Suzuki S; Takagi A; Katsumi A; Hayakawa F; Okamoto S; Suzuki A; Kanematsu T; Matsushita T; Kojima T
Mol Genet Genomic Med; 2020 Sep; 8(9):e1390. PubMed ID: 32627361
[TBL] [Abstract][Full Text] [Related]
6. Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells.
So A; Le Guen T; Lopez BS; Guirouilh-Barbat J
FEBS J; 2017 Aug; 284(15):2324-2344. PubMed ID: 28244221
[TBL] [Abstract][Full Text] [Related]
7. The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.
Kato T; Inagaki H; Miyai S; Suzuki F; Naru Y; Shinkai Y; Kato A; Kanyama K; Mizuno S; Muramatsu Y; Yamamoto T; Shinya M; Tazaki Y; Hiwatashi S; Ikeda T; Ozaki M; Kurahashi H
Hum Genet; 2020 Nov; 139(11):1417-1427. PubMed ID: 32488466
[TBL] [Abstract][Full Text] [Related]
8. The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.
Zhang F; Khajavi M; Connolly AM; Towne CF; Batish SD; Lupski JR
Nat Genet; 2009 Jul; 41(7):849-53. PubMed ID: 19543269
[TBL] [Abstract][Full Text] [Related]
9. Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.
Hsiao MC; Piotrowski A; Alexander J; Callens T; Fu C; Mikhail FM; Claes KB; Messiaen L
Hum Mutat; 2014 Jul; 35(7):891-8. PubMed ID: 24760680
[TBL] [Abstract][Full Text] [Related]
10. The consequences of structural genomic alterations in humans: genomic disorders, genomic instability and cancer.
Colnaghi R; Carpenter G; Volker M; O'Driscoll M
Semin Cell Dev Biol; 2011 Oct; 22(8):875-85. PubMed ID: 21802523
[TBL] [Abstract][Full Text] [Related]
11. Distinct X chromosomal rearrangements in four haemophilia B patients with entire F9 deletion.
Nakamura Y; Ando Y; Takagi Y; Murata M; Kozuka T; Nakata Y; Hasebe R; Takagi A; Matsushita T; Shima M; Kojima T
Haemophilia; 2016 May; 22(3):433-9. PubMed ID: 26686734
[TBL] [Abstract][Full Text] [Related]
12. A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements.
Kohmoto T; Okamoto N; Naruto T; Murata C; Ouchi Y; Fujita N; Inagaki H; Satomura S; Okamoto N; Saito M; Masuda K; Kurahashi H; Imoto I
Mol Cytogenet; 2017; 10():15. PubMed ID: 28465723
[TBL] [Abstract][Full Text] [Related]
13. Mechanisms for human genomic rearrangements.
Gu W; Zhang F; Lupski JR
Pathogenetics; 2008 Nov; 1(1):4. PubMed ID: 19014668
[TBL] [Abstract][Full Text] [Related]
14. Complete F9 Gene Deletion, Duplication, and Triplication Rearrangements: Implications for Factor IX Expression and Clinical Phenotypes.
Ma Y; Li Y; Sun J; Liang Q; Wu R; Ding Q; Dai J
Thromb Haemost; 2024 Apr; 124(4):374-385. PubMed ID: 38011862
[TBL] [Abstract][Full Text] [Related]
15. Ionizing radiation and genetic risks. XVII. Formation mechanisms underlying naturally occurring DNA deletions in the human genome and their potential relevance for bridging the gap between induced DNA double-strand breaks and deletions in irradiated germ cells.
Sankaranarayanan K; Taleei R; Rahmanian S; Nikjoo H
Mutat Res; 2013; 753(2):114-130. PubMed ID: 23948232
[TBL] [Abstract][Full Text] [Related]
16. Complex human chromosomal and genomic rearrangements.
Zhang F; Carvalho CM; Lupski JR
Trends Genet; 2009 Jul; 25(7):298-307. PubMed ID: 19560228
[TBL] [Abstract][Full Text] [Related]
17. Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
Redaelli S; Grati FR; Tritto V; Giannuzzi G; Recalcati MP; Sala E; Villa N; Crosti F; Roversi G; Malvestiti F; Zanatta V; Repetti E; Rodeschini O; Valtorta C; Catusi I; Romitti L; Martinoli E; Conconi D; Dalprà L; Lavitrano M; Riva P; Bentivegna A
HGG Adv; 2024 Apr; 5(2):100261. PubMed ID: 38160254
[TBL] [Abstract][Full Text] [Related]
18. PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1.
Vogt J; Wernstedt A; Ripperger T; Pabst B; Zschocke J; Kratz C; Wimmer K
Eur J Hum Genet; 2016 Nov; 24(11):1598-1604. PubMed ID: 27329736
[TBL] [Abstract][Full Text] [Related]
19. Genomic rearrangements in inherited disease and cancer.
Chen JM; Cooper DN; Férec C; Kehrer-Sawatzki H; Patrinos GP
Semin Cancer Biol; 2010 Aug; 20(4):222-33. PubMed ID: 20541013
[TBL] [Abstract][Full Text] [Related]
20. Identification and characterisation of a novel aberrant pattern of intron 1 inversion with concomitant large insertion and deletion within the F8 gene.
You G; Chi K; Lu Y; Ding Q; Dai J; Xi X; Wang H; Wang X
Thromb Haemost; 2014 Aug; 112(2):264-70. PubMed ID: 24696066
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
