| Tefferi A, Vardiman JW
Myelodysplastic syndromes. [Journal Article, Review]
N Engl J Med 2009 Nov 5; 361(19):1872-85.
Full Citation | Publisher Full Text | Find Related Articles | | Gibson JR, Huber KM, Südhof TC
Neuroligin-2 deletion selectively decreases inhibitory synaptic transmission originating from fast-spiking but not from somatostatin-positive interneurons. [Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
J Neurosci 2009 Nov 4; 29(44):13883-97.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kaeser PS, Deng L, Chávez AE, et al.
ELKS2alpha/CAST deletion selectively increases neurotransmitter release at inhibitory synapses. [In Vitro, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Neuron 2009 Oct 29; 64(2):227-39.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Auvin S, Holder-Espinasse M, Lamblin MD, et al.
Array-CGH detection of a de novo 0.7-Mb deletion in 19p13.13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms. [Case Reports, Letter]
Epilepsia 2009 Nov; 50(11):2501-3.
Full Citation | Publisher Full Text | Find Related Articles | | Morales C, Mademont-Soler I, Armengol L, et al.
Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalities. [Journal Article, Research Support, Non-U.S. Gov't]
Cytogenet Genome Res 2009; 125(4):334-40.
Abstract | Full Citation | | Mahajan D, Prayson RA
Repeated molecular testing in gliomas: a retrospective study of 53 cases. [Journal Article]
Am J Clin Pathol 2009 Jul; 132(1):118-24.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Chen CP, Chern SR, Tsai EJ, et al.
Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations. [Letter, Research Support, Non-U.S. Gov't]
Genet Couns 2009; 20(3):281-8.
Full Citation | Find Related Articles | | Qaksen H, Bartsch O, Okur M, et al.
Rubinstein-Taybi syndrome and CREBBP c.201 202delTA mutation: a case presenting with varicella meningoencephalitis. [Journal Article]
Genet Couns 2009; 20(3):255-60.
Abstract | Full Citation | Find Related Articles | | Bornstein S, White R, Malkoski S, et al.
Smad4 loss in mice causes spontaneous head and neck cancer with increased genomic instability and inflammation. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
J Clin Invest 2009 Nov; 119(11):3408-19.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Fogelstrand P, Féral CC, Zargham R, et al.
Dependence of proliferative vascular smooth muscle cells on CD98hc (4F2hc, SLC3A2). [JOURNAL ARTICLE]
J Exp Med 2009 Oct 19.
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