Normal view MARC view ISBD view

Anisotropic turbulent spectra in the terrestrial magnetosheath as seen by the cluster spacecraft. [electronic resource]

By:

Sahraoui, F

Contributor(s):

Producer: 20060706Description: 075002 p. digitalISSN:

0031-9007

Online resources:

Available from publisher's website

In: Physical review letters vol. 96

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article

There are no comments on this title.

to post a comment.

Back to results

1 Teaching Video NeuroImages: Palatal tremor associated with
by Primiano, Guido
2 Differentiation of Caco-2 cells requires both transcriptional and post-translational down-regulation of Myc.
by Leoni, Bruno Daniele
3 Novel Homozygous KCNJ10 Mutation in a Patient with Non-syndromic Early-Onset Cerebellar Ataxia.
by Nicita, Francesco
4 De novo p.T362R mutation in MORC2 causes early onset cerebellar ataxia, axonal polyneuropathy and nocturnal hypoventilation.
by Zanni, Ginevra
5 Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia.
by Nicita, Francesco
6 Conditioned medium of primary lung cancer cells induces EMT in A549 lung cancer cell line by TGF-ß1 and miRNA21 cooperation.
by Camerlingo, Rosa
7 Identification of novel and hotspot mutations in the channel domain of ITPR1 in two patients with Gillespie syndrome.
by Dentici, Maria Lisa
8 Lamin A/C Is Required for ChAT-Dependent Neuroblastoma Differentiation.
by Guglielmi, Loredana
9 Human placenta-derived neurospheres are susceptible to transformation after extensive in vitro expansion.
by Amendola, Donatella
10 Age and sex prevalence estimate of Joubert syndrome in Italy.
by Nuovo, Sara
11 LMNA knock-down affects differentiation and progression of human neuroblastoma cells.
by Maresca, Giovanna
12 A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect.
by Vicario, Mattia
13 Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
by Travaglini, Lorena
14 Down-regulation of the Lamin A/C in neuroblastoma triggers the expansion of tumor initiating cells.
by Nardella, Marta
15 Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants.
by Nicita, Francesco