Features of Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

被引：85

作者：

Nozaki, Hiroaki ^{[1
]}

Nishizawa, Masatoyo ^{[2
]}

Onodera, Osamu ^{[3
]}

机构：

[1] Niigata Univ, Fac Med, Sch Hlth Sci, Dept Med Technol, Niigata 9518585, Japan

[2] Niigata Univ, Brain Res Inst, Clin Neurosci Branch, Dept Neurol, Niigata 9518585, Japan

[3] Niigata Univ, Dept Mol Neurosci, Resource Branch Brain Dis, Brain Res Inst, Niigata 9518585, Japan

来源：

STROKE | 2014年 / 45卷 / 11期

基金：

日本学术振兴会;

关键词：

cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy; cerebral small vessel diseases; HtrA1; protein; human; myocytes; smooth muscle; TGF-; SMALL-VESSEL DISEASE; HTRA1; MUTATIONS; CARASIL; ALOPECIA; FAMILY; PROTEOLYSIS; EXPRESSION; TGF-BETA-1; PATHOLOGY; PROTEASES;

D O I：

10.1161/STROKEAHA.114.004236

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：3447 / 3453

页数：7

共 45 条

[21] Noncanonical TGFβ Signaling Contributes to Aortic Aneurysm Progression in Marfan Syndrome Mice
Holm, Tammy M.
Habashi, Jennifer P.
Doyle, Jefferson J.
Bedja, Djahida
Chen, YiChun
van Erp, Christel
Lindsay, Mark E.
Kim, David
Schoenhoff, Florian
Cohn, Ronald D.
Loeys, Bart L.
Thomas, Craig J.
Patnaik, Samarjit
Marugan, Juan J.
Judge, Daniel P.
Dietz, Harry C.
[J]. SCIENCE, 2011, 332 (6027) : 358 - 361
[22] The Pathobiology of Vascular Dementia
Iadecola, Costantino
[J]. NEURON, 2013, 80 (04) : 844 - 866
[23] Iwasaki Y, 1997, NEUROL MED, V47, P593
[24] Transforming growth factor β family members in regulation of vascular function: In the light of vascular conditional knockouts
Jakobsson, Lars
van Meeteren, Laurens A.
[J]. EXPERIMENTAL CELL RESEARCH, 2013, 319 (09) : 1264 - 1270
[25] HtrA1-dependent proteolysis of TGF-β controls both neuronal maturation and developmental survival
Launay, S.
Maubert, E.
Lebeurrier, N.
Tennstaedt, A.
Campioni, M.
Docagne, F.
Gabriel, C.
Dauphinot, L.
Potier, M. C.
Ehrmann, M.
Baldi, A.
Vivien, D.
[J]. CELL DEATH AND DIFFERENTIATION, 2008, 15 (09) : 1408 - 1416
[26] Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
Liu, X
Alexander, V
Vijayachandra, K
Bhogte, E
Diamond, I
Glick, A
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) : 9139 - 9144
[27] MAEDA S, 1976, Folia Psychiatrica et Neurologica Japonica, V30, P165
[28] A MISSENSE HTRA1 MUTATION EXPANDS CARASIL SYNDROME TO THE CAUCASIAN POPULATION
Mendioroz, M.
Fernandez-Cadenas, I.
del Rio-Espinola, A.
Rovira, A.
Sole, E.
Fernandez-Figueras, M. T.
Garcia-Patos, V.
Sastre-Garriga, J.
Domingues-Montanari, S.
Alvarez-Sabin, J.
Montaner, J.
[J]. NEUROLOGY, 2010, 75 (22) : 2033 - 2035
[29] A NOVEL MUTATION IN THE HTRA1 GENE CAUSES CARASIL WITHOUT ALOPECIA
Nishimoto, Y.
Shibata, M.
Nihonmatsu, M.
Nozaki, H.
Shiga, A.
Shirata, A.
Yamane, K.
Kosakai, A.
Takahashi, K.
Nishizawa, M.
Onodera, O.
Suzuki, N.
[J]. NEUROLOGY, 2011, 76 (15) : 1353 - 1355
[30] Neuroaxonal integrity evaluated by MR spectroscopy in a case of CARASIL
Nishimoto, Yoshinori
Shibata, Mamoru
Onodera, Osamu
Suzuki, Norihiro
[J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (08) : 860 - 861

← 1 2 3 4 5 →