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Title:	Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia
Source:	Blood [0006-4971] Farrar, Jason yr:2008

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description	2.	Faivre, L. "Detection of an Interstitial 3q21.1-q21.3 Deletion in a Child With Multiple Congenital Abnormalities, Mental Retardation, Pancytopenia, and Myelodysplasia." American journal of medical genetics. Part A 149A.6 (2009): 1323-1326.
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description	4.	Miyake, K. "Ribosomal protein S19 deficiency leads to reduced proliferation and increased apoptosis but does not affect terminal erythroid differentiation in a cell line model of Diamond-Blackfan anemia." Stem cells 26.2 (2008): 323-329.
description	5.	Adler, Lenard A A. "Functional outcomes in the treatment of adults with ADHD." Journal of attention disorders 11.6 (2008): 720-727.
description	6.	Hannon, G. "RNA interference." Nature 418.6894 (2002): 244-251.
description	7.	Elbashir, S M M. "RNA interference is mediated by 21- and 22-nucleotide RNAs." Genes & development 15.2: 188-200.
description	8.	fire, A. "potent and specific genetic interference by double-stranded RNA in caenorhabditis elegans." Nature 391.6669: 806-811.
description	9.	Zamore, P D D. "RNAi: double-stranded RNA directs the ATP-dependent cleavage of mRNA at 21 to 23 nucleotide intervals." Cell 101.1 (2000): 25-33.
description	10.	Dorsett, Y. "siRNAs: applications in functional genomics and potential as therapeutics." Nature reviews. Drug discovery 3.4 (2004): 318-29.
description	11.	Matza, L.S. S. "Responsiveness of the Adult Attention-Deficit/Hyperactivity Disorder Quality of Life Scale (AAQoL)." Quality of life research 16.9: 1511-1520.
description	12.	Molin, A-M M. "A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features." Journal of medical genetics 49.2 (2012): 104-109.
description	13.	Sussman, N. "Treatment of Attention-Deficit/Hyperactivity Disorder." Primary psychiatry 14.1 (2007): 39-42.
description	14.	Wilson, Golder N. "Interstitial deletion 5q14.3q21.3 with MEF2C haploinsufficiency and mild phenotype: when more is less." American journal of medical genetics. Part A 155A.6 (2011): 1437-1441.
description	15.	Willemsen, Marjolein H. "Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions." American journal of medical genetics. Part A 155.1 (2011): 106-112.
description	16.	Sieff, Colin A. "Pathogenesis of the erythroid failure in Diamond Blackfan anaemia." British journal of haematology 148.4 (2009): 611-622.
description	17.	Manouvrier, S. "Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype." Clinical genetics 55.2 (1999): 127-129.
description	18.	Cmejla, R. "Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia." Human mutation 28.12 (2007): 1178-1182.
description	19.	Ciovacco, Melissa A. "Human phenotypes associated with GATA-1 mutations." Gene 427.1-2 (2008): 1-6.
description	20.	Danilova, N. "Ribosomal protein S19 deficiency in zebrafish leads to developmental abnormalities and defective erythropoiesis through activation of p53 protein family." Blood 112.13 (2008): 5228-5237.