| DONSON facilitates Cdc45 and GINS chromatin association and is essential for DNA replication initiation. | DONSON facilitates Cdc45 and GINS chromatin association and is essential for DNA replication initiation.
Kingsley G, Skagia A, Passaretti P, Fernandez-Cuesta C, Reynolds-Winczura A, Koscielniak K, Gambus A., Free PMC Article | 02/5/2024 |
| DONSON is required for CMG helicase assembly in the mammalian cell cycle. | DONSON is required for CMG helicase assembly in the mammalian cell cycle.
Evrin C, Alvarez V, Ainsworth J, Fujisawa R, Alabert C, Labib KP., Free PMC Article | 11/7/2023 |
| Novel role of DONSON in CMG helicase assembly during vertebrate DNA replication initiation. | Novel role of DONSON in CMG helicase assembly during vertebrate DNA replication initiation.
Hashimoto Y, Sadano K, Miyata N, Ito H, Tanaka H., | 09/6/2023 |
| Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome. | Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome.
Knapp KM, Sullivan R, Murray J, Gimenez G, Arn P, D'Souza P, Gezdirici A, Wilson WG, Jackson AP, Ferreira C, Bicknell LS., Free PMC Article | 02/27/2021 |
| Circ-DONSON promotes malignant progression of glioma through modulating FOXO3. | Circ-DONSON promotes malignant progression of glioma through modulating FOXO3.
Zou Z, Dong YS, Liu JM, Zhao ZH, Li G, Liu DD. | 02/13/2021 |
| DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain. | DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain.
Zhang J, Bellani MA, James RC, Pokharel D, Zhang Y, Reynolds JJ, McNee GS, Jackson AP, Stewart GS, Seidman MM., Free PMC Article | 09/26/2020 |
| four unrelated families with five affected individuals having biallelic or de novo variants in DONSON presenting with a core phenotype of severe short stature (z score < -3 SD), additional skeletal abnormalities, and microcephaly, were identified. | Biallelic and De Novo Variants in DONSON Reveal a Clinical Spectrum of Cell Cycle-opathies with Microcephaly, Dwarfism and Skeletal Abnormalities.
Karaca E, Posey JE, Bostwick B, Liu P, Gezdirici A, Yesil G, Coban Akdemir Z, Bayram Y, Harms FL, Meinecke P, Alawi M, Bacino CA, Sutton VR, Kortüm F, Lupski JR., Free PMC Article | 08/12/2020 |
| we present the clinical data of siblings with microcephaly, short stature, and limb abnormalities syndrome (MISSLA) featuring a novel DONSON variant and summarize the current literature on MISSLA. | Differentiation of MISSLA and Fanconi anaemia by computer-aided image analysis and presentation of two novel MISSLA siblings.
Danyel M, Cheng Z, Jung C, Boschann F, Pantel JT, Hajjir N, Flöttmann R, Schulz S, Demuth I, Sheridan E, Mundlos S, Horn D, Mensah MA., Free PMC Article | 07/18/2020 |
| the antitumor miR-101-5p/DONSON axis and its modulated replisome genes might be a novel diagnostic and therapeutic target for clear cell renal cell carcinoma | Replisome genes regulation by antitumor miR-101-5p in clear cell renal cell carcinoma.
Yamada Y, Nohata N, Uchida A, Kato M, Arai T, Moriya S, Mizuno K, Kojima S, Yamazaki K, Naya Y, Ichikawa T, Seki N., Free PMC Article | 04/25/2020 |
| Aberrant splicing and a noncoding mutation in DONSON gene is the cause of microcephaly-micromelia syndrome | Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.
Evrony GD, Cordero DR, Shen J, Partlow JN, Yu TW, Rodin RE, Hill RS, Coulter ME, Lam AN, Jayaraman D, Gerrelli D, Diaz DG, Santos C, Morrison V, Galli A, Tschulena U, Wiemann S, Martel MJ, Spooner B, Ryu SC, Elhosary PC, Richardson JM, Tierney D, Robinson CA, Chibbar R, Diudea D, Folkerth R, Wiebe S, Barkovich AJ, Mochida GH, Irvine J, Lemire EG, Blakley P, Walsh CA., Free PMC Article | 06/2/2018 |