192 related articles for article (PubMed ID: 21660439)
21. Hematologically important mutations: Shwachman-Diamond syndrome.
Costa E; Santos R
Blood Cells Mol Dis; 2008; 40(2):183-4. PubMed ID: 17916435
[TBL] [Abstract][Full Text] [Related]
22. The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA.
Ganapathi KA; Austin KM; Lee CS; Dias A; Malsch MM; Reed R; Shimamura A
Blood; 2007 Sep; 110(5):1458-65. PubMed ID: 17475909
[TBL] [Abstract][Full Text] [Related]
23. M phase-specific interaction between SBDS and RNF2 at the mitotic spindles regulates mitotic progression.
Sera Y; Imanaka T; Yamaguchi M
Biochem Biophys Res Commun; 2023 Nov; 682():118-123. PubMed ID: 37806249
[TBL] [Abstract][Full Text] [Related]
24. [Shwachman-Diamond syndrome].
Vinokurova LV; Dubtsova EA; Yashina NI; Shulyatyev IS; Osipenko YV
Ter Arkh; 2014; 86(2):72-5. PubMed ID: 24772512
[TBL] [Abstract][Full Text] [Related]
25. Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients.
Minelli A; Nacci L; Valli R; Pietrocola G; Ramenghi U; Locatelli F; Brescia L; Nicolis E; Cipolli M; Danesino C
Blood Cells Mol Dis; 2016 Sep; 60():33-5. PubMed ID: 27519942
[No Abstract] [Full Text] [Related]
26. In Vivo Senescence in the Sbds-Deficient Murine Pancreas: Cell-Type Specific Consequences of Translation Insufficiency.
Tourlakis ME; Zhang S; Ball HL; Gandhi R; Liu H; Zhong J; Yuan JS; Guidos CJ; Durie PR; Rommens JM
PLoS Genet; 2015 Jun; 11(6):e1005288. PubMed ID: 26057580
[TBL] [Abstract][Full Text] [Related]
27. The Greek Registry of Shwachman Diamond-Syndrome: Molecular and clinical data.
Delaporta P; Sofocleous C; Economou M; Makis A; Kostaridou S; Kattamis A
Pediatr Blood Cancer; 2017 Nov; 64(11):. PubMed ID: 28509441
[TBL] [Abstract][Full Text] [Related]
28. Sbds is required for Rac2-mediated monocyte migration and signaling downstream of RANK during osteoclastogenesis.
Leung R; Cuddy K; Wang Y; Rommens J; Glogauer M
Blood; 2011 Feb; 117(6):2044-53. PubMed ID: 21084708
[TBL] [Abstract][Full Text] [Related]
29. Direct interaction between EFL1 and SBDS is mediated by an intrinsically disordered insertion domain.
Asano N; Atsuumi H; Nakamura A; Tanaka Y; Tanaka I; Yao M
Biochem Biophys Res Commun; 2014 Jan; 443(4):1251-6. PubMed ID: 24406167
[TBL] [Abstract][Full Text] [Related]
30. Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome.
Finch AJ; Hilcenko C; Basse N; Drynan LF; Goyenechea B; Menne TF; González Fernández A; Simpson P; D'Santos CS; Arends MJ; Donadieu J; Bellanné-Chantelot C; Costanzo M; Boone C; McKenzie AN; Freund SM; Warren AJ
Genes Dev; 2011 May; 25(9):917-29. PubMed ID: 21536732
[TBL] [Abstract][Full Text] [Related]
31. Radiosensitivity in lymphoblastoid cell lines derived from Shwachman-Diamond syndrome patients.
Morini J; Babini G; Mariotti L; Baiocco G; Nacci L; Maccario C; Rößler U; Minelli A; Savio M; Gomolka M; Kulka U; Ottolenghi A; Danesino C
Radiat Prot Dosimetry; 2015 Sep; 166(1-4):95-100. PubMed ID: 25870433
[TBL] [Abstract][Full Text] [Related]
32. Ubiquitin-proteasome-rich cytoplasmic structures in neutrophils of patients with Shwachman-Diamond syndrome.
Necchi V; Minelli A; Sommi P; Vitali A; Caruso R; Longoni D; Frau MR; Nasi C; De Gregorio F; Zecca M; Ricci V; Danesino C; Solcia E
Haematologica; 2012 Jul; 97(7):1057-63. PubMed ID: 22271888
[TBL] [Abstract][Full Text] [Related]
33. The Shwachman-Diamond SBDS protein localizes to the nucleolus.
Austin KM; Leary RJ; Shimamura A
Blood; 2005 Aug; 106(4):1253-8. PubMed ID: 15860664
[TBL] [Abstract][Full Text] [Related]
34. Ribosomal biogenesis genes play an essential and p53-independent role in zebrafish pancreas development.
Provost E; Wehner KA; Zhong X; Ashar F; Nguyen E; Green R; Parsons MJ; Leach SD
Development; 2012 Sep; 139(17):3232-41. PubMed ID: 22872088
[TBL] [Abstract][Full Text] [Related]
35. Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes.
Zambetti NA; Bindels EM; Van Strien PM; Valkhof MG; Adisty MN; Hoogenboezem RM; Sanders MA; Rommens JM; Touw IP; Raaijmakers MH
Haematologica; 2015 Oct; 100(10):1285-93. PubMed ID: 26185170
[TBL] [Abstract][Full Text] [Related]
36. Of blood, bones, and ribosomes: is Swachman-Diamond syndrome a ribosomopathy?
Johnson AW; Ellis SR
Genes Dev; 2011 May; 25(9):898-900. PubMed ID: 21536731
[TBL] [Abstract][Full Text] [Related]
37. Exploring the role of elongation Factor-Like 1 (EFL1) in Shwachman-Diamond syndrome through molecular dynamics.
Delre P; Alberga D; Gijsbers A; Sánchez-Puig N; Nicolotti O; Saviano M; Siliqi D; Mangiatordi GF
J Biomol Struct Dyn; 2020 Oct; 38(17):5219-5229. PubMed ID: 31838967
[TBL] [Abstract][Full Text] [Related]
38. Diagnosis, Treatment, and Molecular Pathology of Shwachman-Diamond Syndrome.
Nelson AS; Myers KC
Hematol Oncol Clin North Am; 2018 Aug; 32(4):687-700. PubMed ID: 30047420
[TBL] [Abstract][Full Text] [Related]
39. Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome.
Woloszynek JR; Rothbaum RJ; Rawls AS; Minx PJ; Wilson RK; Mason PJ; Bessler M; Link DC
Blood; 2004 Dec; 104(12):3588-90. PubMed ID: 15284109
[TBL] [Abstract][Full Text] [Related]
40. [Two cases of Shwachman-Diamond syndrome with genetic confirmation and literature review].
Shen J; Lin K; An Y; Wu YM; Qiao ZW; Yu H; Zhu QR; Zhang T
Zhonghua Er Ke Za Zhi; 2013 Sep; 51(9):679-83. PubMed ID: 24330988
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
