Citations for
1DTNA
Absence of glial α-dystrobrevin causes abnormalities of the blood-brain barrier and progressive brain edema.
Lien CF, Mohanta SK, Frontczak-Baniewicz M, Swinny JD, Zablocka B, Górecki DC.
J Biol Chem 287(49):41374-85. doi: 10.1074/jbc.M112.400044. Epub 2012 Oct 5. 2012
2DTNA, ERBB2, ERBB4, NRG1
Neuregulin/ErbB regulate neuromuscular junction development by phosphorylation of α-dystrobrevin.
Schmidt N, Akaaboune M, Gajendran N, Martinez-Pena y Valenzuela I, Wakefield S, Thurnheer R, Brenner HR.
J Cell Biol 195(7):1171-84. doi: 10.1083/jcb.201107083. Epub 2011 Dec 19. 2011
3CTNNAL1, DTNA
Alpha-dystrobrevin-1 recruits alpha-catulin to the alpha1D-adrenergic receptor/dystrophin-associated protein complex signalosome.
Lyssand JS, Whiting JL, Lee KS, Kastl R, Wacker JL, Bruchas MR, Miyatake M, Langeberg LK, Chavkin C, Scott JD, Gardner RG, Adams ME, Hague C.
Proc Natl Acad Sci U S A 107(50):21854-9. doi: 10.1073/pnas.1010819107. Epub 2010 Nov 29. 2010
4DTNA
Dystrophin-associated protein scaffolding in brain requires alpha-dystrobrevin.
Bragg AD, Das SS, Froehner SC.
Neuroreport 21(10):695-9. doi: 10.1097/WNR.0b013e32833b0a3b. 2010
5DTNA
Synaptic alpha-dystrobrevin: localization of a short alpha-dystrobrevin isoform in melanin-concentrating hormone neurons of the hypothalamus.
Hazai D, Lien CF, Hajós F, Halasy K, Górecki DC, Jancsik V.
Brain Res 1201:52-9. doi: 10.1016/j.brainres.2008.01.046. Epub 2008 Jan 26. 2008
6DTNA
Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.
Nakamori M, Kimura T, Kubota T, Matsumura T, Sumi H, Fujimura H, Takahashi MP, Sakoda S.
Neurology 70(9):677-85. doi: 10.1212/01.wnl.0000302174.08951.cf. 2008
7DTNA, DTNB
Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin.
Grady RM, Wozniak DF, Ohlemiller KK, Sanes JR.
J Neurosci 26(11):2841-51. 2006
8DTNA
The syntrophin-dystrobrevin subcomplex in human neuromuscular disorders.
Compton AG, Cooper ST, Hill PM, Yang N, Froehner SC, North KN.
J Neuropathol Exp Neurol 64(4):350-61. 2005
9TAZ, DTNA, INVM, LVNC
Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.
Kenton AB, Sanchez X, Coveler KJ, Makar KA, Jimenez S, Ichida F, Murphy RT, Elliott PM, McKenna W, Bowles NE, Towbin JA, Bowles KR.
Mol Genet Metab 82(2):162-6. 2004
10DTNA, DTNB, MAGEE1
DAMAGE, a novel alpha-dystrobrevin-associated MAGE protein in dystrophin complexes.
Albrecht DE, Froehner SC.
J Biol Chem 279(8):7014-23. Epub 2003 Nov 17. 2004
11DTNA
Characterization of human alpha-dystrobrevin isoforms in HL-60 human promyelocytic leukemia cells undergoing granulocytic differentiation.
Kulyte A, Navakauskiene R, Treigyte G, Gineitis A, Bergman T, Magnusson KE.
Mol Biol Cell 13(12):4195-205. 2002
12DTNA
A novel mechanism for modulating synaptic gene expression: differential localization of alpha-dystrobrevin transcripts in skeletal muscle.
Newey SE, Gramolini AO, Wu J, Holzfeind P, Jasmin BJ, Davies KE, Blake DJ.
Mol Cell Neurosci 17(1):127-40. 2001
13BTHS2, DTNA, BTHS, LVNC, TAZ
Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome.
Ichida F, Tsubata S, Bowles KR, Haneda N, Uese K, Miyawaki T, Dreyer WJ, Messina J, Li H, Bowles NE, Towbin JA.
Circulation 103(9):1256-63. 2001
14DTNA
Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy.
Yoshida M, Hama H, Ishikawa-Sakurai M, Imamura M, Mizuno Y, Araishi K, Wakabayashi-Takai E, Noguchi S, Sasaoka T, Ozawa E.
Hum Mol Genet 9(7):1033-40. 2000
15DTNA
Dystrobrevin localization in photoreceptor axon terminals and at blood-ocular barrier sites.
Ueda H, Baba T, Kashiwagi K, Iijima H, Ohno S.
Invest Ophthalmol Vis Sci 41(12):3908-14. 2000
16DTNA, DTNB
Different dystrophin-like complexes are expressed in neurons and glia.
Blake DJ, Hawkes R, Benson MA, Beesley PW.
J Cell Biol 147(3):645-58. 1999
17DTNA
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.
Metzinger L, Blake DJ, Squier MV, Anderson LV, Deconinck AE, Nawrotzki R, Hilton-Jones D, Davies KE.
Hum Mol Genet 6(7):1185-91. 1997
18DTNA
The genomic organization of human dystrobrevin.
Sadoulet-Puccio HM, et al.
Neurogenetics 1 : 37-42. 1997
19DTNA
Dystrobrevin and dystrophin : an interaction through coiled-coil motifs.
Sadoulet-Puccio HM, Rajala M, Kunkel LM.
Proc Natl Acad Sci U S A 94(23):12413-8. 1997
20DTNA, LVNC
Isolated noncompaction of the myocardium in adults.
Ritter M, Oechslin E, Sutsch G, Attenhofer C, Schneider J, Jenni R.
Mayo Clin Proc 72(1):26-31. 1997
21DTNA
Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane.
Sadoulet-Puccio HM, et al.
Hum Mol Genet 5 : 489-496. 1996
22DTNA
(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein.
Khurana TS, et al.
Hum Mol Genet 3 : 841. 1994