A Messing
Overview
Explore the profile of A Messing including associated specialties, affiliations and a list of published articles.
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Articles
77
Citations
3118
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Recent Articles
1.
Messing A, Behringer R, Slapak J, Lemke G, Palmiter R, Brinster R
Mouse Genome
. 2014 Oct;
87:107.
PMID: 25346577
No abstract available.
2.
Prust M, Wang J, Morizono H, Messing A, Brenner M, Gordon E, et al.
Neurology
. 2011 Sep;
77(13):1287-94.
PMID: 21917775
Objective: To characterize Alexander disease (AxD) phenotypes and determine correlations with age at onset (AAO) and genetic mutation. AxD is an astrogliopathy usually characterized on MRI by leukodystrophy and caused...
3.
Connor J, McCormack K, Pletsch A, Gaeta S, Ganetzky B, Chiu S, et al.
Genes Brain Behav
. 2005 Feb;
4(2):77-88.
PMID: 15720404
Shaker-type potassium (K+) channels are composed of pore-forming alpha subunits associated with cytoplasmic beta subunits. Kv beta2 is the predominant Kv beta subunit in the mammalian nervous system, but its...
4.
Gorospe J, Naidu S, Johnson A, Puri V, Raymond G, Jenkins S, et al.
Neurology
. 2002 May;
58(10):1494-500.
PMID: 12034785
Background And Objective: Alexander disease is a slowly progressive CNS disorder that most commonly occurs in children. Until recently, the diagnosis could only be established by the histologic finding of...
5.
Messing A, Brenner M, Johnson A, Goldman J
Pediatr Neurol
. 2001 Nov;
25(4):347-8; author reply 348.
PMID: 11704412
No abstract available.
6.
Zhuo L, Theis M, Alvarez-Maya I, Brenner M, Willecke K, Messing A
Genesis
. 2001 Oct;
31(2):85-94.
PMID: 11668683
With the goal of performing astrocyte-specific modification of genes in the mouse, we have generated a transgenic line expressing Cre recombinase under the control of the human glial fibrillary acidic...
7.
Rodriguez D, Gauthier F, Bertini E, Bugiani M, Brenner M, Nguyen S, et al.
Am J Hum Genet
. 2001 Sep;
69(5):1134-40.
PMID: 11567214
Heterozygous, de novo mutations in the glial fibrillary acidic protein (GFAP) gene have recently been reported in 12 patients affected by neuropathologically proved Alexander disease. We searched for GFAP mutations...
8.
Messing A, Goldman J, Johnson A, Brenner M
J Neuropathol Exp Neurol
. 2001 Jun;
60(6):563-73.
PMID: 11398833
Prior to finding that GFAP mutations underlie many cases of Alexander disease, it was unclear whether the disease originated in astrocytes or if the formation of Rosenthal fibers was a...
9.
Brenner M, Johnson A, Boespflug-Tanguy O, Rodriguez D, Goldman J, Messing A
Nat Genet
. 2001 Jan;
27(1):117-20.
PMID: 11138011
Alexander disease is a rare disorder of the central nervous system of unknown etiology. Infants with Alexander disease develop a leukoencephalopathy with macrocephaly, seizures and psychomotor retardation, leading to death...
10.
Previtali S, Quattrini A, Fasolini M, Panzeri M, Villa A, Filbin M, et al.
J Cell Biol
. 2000 Nov;
151(5):1035-46.
PMID: 11086005
In peripheral nerve myelin, the intraperiod line results from compaction of the extracellular space due to homophilic adhesion between extracellular domains (ECD) of the protein zero (P(0)) glycoprotein. Point mutations...