131 related articles for article (PubMed ID: 31908654)
1. Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype.
Khan AW; Minelli A; Frattini A; Montalbano G; Bogni A; Fabbri M; Porta G; Acquati F; Pinto RM; Bergami E; Mura R; Pegoraro A; Cesaro S; Cipolli M; Zecca M; Danesino C; Locatelli F; Maserati E; Pasquali F; Valli R
Mol Cytogenet; 2020; 13():1. PubMed ID: 31908654
[TBL] [Abstract][Full Text] [Related]
2. The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations.
Khan AW; Kennedy A; Furutani E; Myers K; Frattini A; Acquati F; Roccia P; Micheloni G; Minelli A; Porta G; Cipolli M; Cesaro S; Danesino C; Pasquali F; Shimamura A; Valli R
Mol Cytogenet; 2021 Nov; 14(1):54. PubMed ID: 34819134
[TBL] [Abstract][Full Text] [Related]
3. Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.
Valli R; De Paoli E; Nacci L; Frattini A; Pasquali F; Maserati E
Pediatr Blood Cancer; 2017 Aug; 64(8):. PubMed ID: 28130858
[TBL] [Abstract][Full Text] [Related]
4. Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability.
Valli R; Minelli A; Galbiati M; D'Amico G; Frattini A; Montalbano G; Khan AW; Porta G; Millefanti G; Olivieri C; Cipolli M; Cesaro S; Pasquali F; Danesino C; Cazzaniga G; Maserati E
Br J Haematol; 2019 Mar; 184(6):974-981. PubMed ID: 30585299
[TBL] [Abstract][Full Text] [Related]
5. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Maserati E; Pressato B; Valli R; Minelli A; Sainati L; Patitucci F; Marletta C; Mastronuzzi A; Poli F; Lo Curto F; Locatelli F; Danesino C; Pasquali F
Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
[TBL] [Abstract][Full Text] [Related]
6. Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms.
Valli R; Pressato B; Marletta C; Mare L; Montalbano G; Curto FL; Pasquali F; Maserati E
Mol Cytogenet; 2013 Dec; 6(1):56. PubMed ID: 24330778
[TBL] [Abstract][Full Text] [Related]
7. Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene.
Nacci L; Valli R; Maria Pinto R; Zecca M; Cipolli M; Morini J; Cesaro S; Boveri E; Rosti V; Corti P; Ambroni M; Pasquali F; Danesino C; Maserati E; Minelli A
Genes Chromosomes Cancer; 2017 Jan; 56(1):51-58. PubMed ID: 27553422
[TBL] [Abstract][Full Text] [Related]
8. Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Maserati E; Minelli A; Pressato B; Valli R; Crescenzi B; Stefanelli M; Menna G; Sainati L; Poli F; Panarello C; Zecca M; Curto FL; Mecucci C; Danesino C; Pasquali F
Genes Chromosomes Cancer; 2006 Apr; 45(4):375-82. PubMed ID: 16382447
[TBL] [Abstract][Full Text] [Related]
9. The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
Minelli A; Maserati E; Nicolis E; Zecca M; Sainati L; Longoni D; Lo Curto F; Menna G; Poli F; De Paoli E; Cipolli M; Locatelli F; Pasquali F; Danesino C
Leukemia; 2009 Apr; 23(4):708-11. PubMed ID: 19148133
[TBL] [Abstract][Full Text] [Related]
10. Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
Maserati E; Minelli A; Olivieri C; Bonvini L; Marchi A; Bozzola M; Danesino C; Scappaticci S; Pasquali F
Cancer Genet Cytogenet; 2000 Sep; 121(2):167-71. PubMed ID: 11063802
[TBL] [Abstract][Full Text] [Related]
11. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Sokolic RA; Ferguson W; Mark HF
Cancer Genet Cytogenet; 1999 Dec; 115(2):106-13. PubMed ID: 10598142
[TBL] [Abstract][Full Text] [Related]
12. Does isochromosome 7q mandate bone marrow transplant in children with Shwachman-Diamond syndrome?
Cunningham J; Sales M; Pearce A; Howard J; Stallings R; Telford N; Wilkie R; Huntly B; Thomas A; O'Marcaigh A; Will A; Pratt N
Br J Haematol; 2002 Dec; 119(4):1062-9. PubMed ID: 12472589
[TBL] [Abstract][Full Text] [Related]
13. Monitoring the isochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR.
Porta G; Mattarucchi E; Maserati E; Pressato B; Valli R; Morerio C; Zecca M; Panarello C; Locatelli F; Lo Curto F; Pasquali F
J Pediatr Hematol Oncol; 2007 Mar; 29(3):163-5. PubMed ID: 17356395
[TBL] [Abstract][Full Text] [Related]
14.
Mourad S; Bilodeau M; Roussy M; Laramée L; Boulianne L; Rouette A; Jouan L; Gendron P; Duval M; Teira P; Hébert J; Bittencourt H; Pastore Y; Landry JR; Cellot S
Front Oncol; 2019; 9():772. PubMed ID: 31475115
[TBL] [Abstract][Full Text] [Related]
15. Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: a prospective 5-year follow-up study.
Dror Y; Durie P; Ginzberg H; Herman R; Banerjee A; Champagne M; Shannon K; Malkin D; Freedman MH
Exp Hematol; 2002 Jul; 30(7):659-69. PubMed ID: 12135662
[TBL] [Abstract][Full Text] [Related]
16. Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cells.
Ruiz-Gutierrez M; Bölükbaşı ÖV; Alexe G; Kotini AG; Ballotti K; Joyce CE; Russell DW; Stegmaier K; Myers K; Novina CD; Papapetrou EP; Shimamura A
JCI Insight; 2019 Apr; 5(12):. PubMed ID: 31039138
[TBL] [Abstract][Full Text] [Related]
17. [Cytogenetic characteristics of hematopoietic and stromal progenitor cells in myelodysplastic syndrome].
Pimenova MA; Parovichnikova EN; Kokhno AV; Domracheva EV; Manakova TE; Mal'tseva IuS; Konnova ML; Shishigina LA; Savchenko VG
Ter Arkh; 2013; 85(7):34-42. PubMed ID: 24137945
[TBL] [Abstract][Full Text] [Related]
18. Ataluren-driven restoration of Shwachman-Bodian-Diamond syndrome protein function in Shwachman-Diamond syndrome bone marrow cells.
Bezzerri V; Bardelli D; Morini J; Vella A; Cesaro S; Sorio C; Biondi A; Danesino C; Farruggia P; Assael BM; D'amico G; Cipolli M
Am J Hematol; 2018 Aug; 93(4):527-536. PubMed ID: 29285795
[TBL] [Abstract][Full Text] [Related]
19. A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome.
Cesaro S; Pegoraro A; Sainati L; Lucidi V; Montemitro E; Corti P; Ramenghi U; Nasi C; Menna G; Zecca M; Danesino C; Nicolis E; Pasquali F; Perobelli S; Tridello G; Farruggia P; Cipolli M
J Pediatr; 2020 Apr; 219():196-201.e1. PubMed ID: 32037152
[TBL] [Abstract][Full Text] [Related]
20. SBDS mutations and isochromosome 7q in a patient with Shwachman-Diamond syndrome: no predisposition to malignant transformation?
Mellink CH; Alders M; van der Lelie H; Hennekam RH; Kuijpers TW
Cancer Genet Cytogenet; 2004 Oct; 154(2):144-9. PubMed ID: 15474150
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
