Valli R - Search Results

1

Enhanced p53 Levels Are Involved in the Reduced Mineralization Capacity of Osteoblasts Derived from Shwachman-Diamond Syndrome Subjects.

Frattini A, Bolamperti S, Valli R, Cipolli M, Pinto RM, Bergami E, Frau MR, Cesaro S, Signo M, Bezzerri V, Porta G, Khan AW, Rubinacci A, Villa I. Frattini A, et al. Among authors: valli r. Int J Mol Sci. 2021 Dec 11;22(24):13331. doi: 10.3390/ijms222413331. Int J Mol Sci. 2021. PMID: 34948128 Free PMC article.

2

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. Porta G, et al. Among authors: valli r. J Pediatr Hematol Oncol. 2007 Mar;29(3):163-5. doi: 10.1097/MPH.0b013e31803b958e. J Pediatr Hematol Oncol. 2007. PMID: 17356395

3

A homozygous contiguous gene deletion in chromosome 16p13.3 leads to autosomal recessive osteopetrosis in a Jordanian patient.

Pangrazio A, Frattini A, Valli R, Maserati E, Susani L, Vezzoni P, Villa A, Al-Herz W, Sobacchi C. Pangrazio A, et al. Among authors: valli r. Calcif Tissue Int. 2012 Oct;91(4):250-4. doi: 10.1007/s00223-012-9631-4. Epub 2012 Jul 31. Calcif Tissue Int. 2012. PMID: 22847576

4

Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome.

Nacci L, Danesino C, Sainati L, Longoni D, Poli F, Cipolli M, Perobelli S, Nicolis E, Cannioto Z, Morini J, Valli R, Pasquali F, Minelli A. Nacci L, et al. Among authors: valli r. Br J Haematol. 2014 May;165(4):573-5. doi: 10.1111/bjh.12767. Epub 2014 Feb 1. Br J Haematol. 2014. PMID: 24484588 Free article. No abstract available.

5

Cytogenetic monitoring in Shwachman-Diamond syndrome: a note on clonal progression and a practical warning.

Pressato B, Valli R, Marletta C, Mare L, Montalbano G, Curto FL, Pasquali F, Maserati E. Pressato B, et al. Among authors: valli r. J Pediatr Hematol Oncol. 2015 May;37(4):307-10. doi: 10.1097/MPH.0000000000000268. J Pediatr Hematol Oncol. 2015. PMID: 25887640

6

Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature.

Valli R, De Bernardi F, Frattini A, Volpi L, Bignami M, Facchetti F, Pasquali F, Castelnuovo P, Maserati E. Valli R, et al. Genes Chromosomes Cancer. 2015 Dec;54(12):771-5. doi: 10.1002/gcc.22288. Epub 2015 Sep 10. Genes Chromosomes Cancer. 2015. PMID: 26355525 Review.

7

High variability of genomic instability and gene expression profiling in different HeLa clones.

Frattini A, Fabbri M, Valli R, De Paoli E, Montalbano G, Gribaldo L, Pasquali F, Maserati E. Frattini A, et al. Among authors: valli r. Sci Rep. 2015 Oct 20;5:15377. doi: 10.1038/srep15377. Sci Rep. 2015. PMID: 26483214 Free PMC article.

8

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. Minelli A, et al. Among authors: valli r. Blood Cells Mol Dis. 2016 Sep;60:33-5. doi: 10.1016/j.bcmd.2016.06.007. Epub 2016 Jun 22. Blood Cells Mol Dis. 2016. PMID: 27519942 Free article. No abstract available.

9

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. Nacci L, et al. Among authors: valli r. Genes Chromosomes Cancer. 2017 Jan;56(1):51-58. doi: 10.1002/gcc.22401. Epub 2016 Sep 21. Genes Chromosomes Cancer. 2017. PMID: 27553422

10

Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.

Valli R, De Paoli E, Nacci L, Frattini A, Pasquali F, Maserati E. Valli R, et al. Pediatr Blood Cancer. 2017 Aug;64(8). doi: 10.1002/pbc.26454. Epub 2017 Jan 28. Pediatr Blood Cancer. 2017. PMID: 28130858

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