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15.Rat olfactory bulb and epithelium UDP-glucuronosyltransferase 2A1 (UGT2A1) 4 c& I% F6 ?/ X% H* J! d
expression: in situ mRNA localization and quantitative analysis.
5 H4 c  w/ K& }; I, W- q10.Epilepsy, progessive movement disorder and cognitive decline.9 G# V4 H+ B1 c5 t
11.A neuropathological study of autosomal-dominant chorea-acanthocytosis with a mutation of VPS13A.+ k& P7 O8 y+ V0 o
16.Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C.
+ X, j4 h  s1 \$ |26.[Genetic studies on mental disorders: recent topics on clinical and molecular genetics].9 T6 s/ M, F- V' m9 {
29.Analysis of the human VPS13 gene family.$ Z0 \6 J/ X/ \1 l
4.The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules.) |5 B( V  u  Z9 m1 L" L
5.Neuronal pentraxin receptor in cerebrospinal fluid as a potential biomarker for neurodegenerative diseases.4 d' {1 G. S1 [% [  c
16.The neuronal growth and regeneration associated Cntn1 (F3/F11/Contactin) gene is duplicated in fish: expression during development and retinal axon regeneration.
, [/ t: ?0 H+ y18.Transgenic mice expressing F3/contactin from the TAG-1 promoter exhibit developmentally regulated changes in the differentiation of cerebellar neurons.
! u' W+ R: y. h5 X- `. @8.MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization./ }( C) `* z8 ]6 i4 _% F
3.IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervous system.
% r3 _2 [3 s% j2 r4.Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation.; s( k! X5 B  z" S1 ^. o1 I

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xinqing0927

15.Rat olfactory bulb and epithelium UDP-glucuronosyltransferase 2A1 (UGT2A1) expression: in situ mRNA localization and quantitative analysis.' w4 x$ ?' N" S: t! U! ]4 H. L
Heydel J, Leclerc S, Bernard P, Pelczar H, Gradinaru D, Magdalou J, Minn A, Artur Y, Goudonnet H.6 R7 s- G/ m# V- e: z2 x: m0 t$ ~
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10.Epilepsy, progessive movement disorder and cognitive decline.
# T  s0 o0 j: J' lRobertson B, Evans AH, Walterfang M, Ng AP, Velakoulis D.
' A6 @" t* V9 b4 VJ Clin Neurosci. 2008 Jul;15(7):812. No abstract available.
/ |$ t; X: V9 D0 [4 U) zPMID: 18589883 [PubMed - indexed for MEDLINE]# z; n/ v. ~' _6 o: w* |( x

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11.A neuropathological study of autosomal-dominant chorea-acanthocytosis with a mutation of VPS13A.Ishida C, Makifuchi T, Saiki S, Hirose G, Yamada M.
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16.Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C.Mizuno E, Nakamura M, Agemura A, Kusumoto A, Ichiba M, Kurano Y, Muroya S, Sano A.2 O# |" w( _9 ^- c+ j* I

( i# t! S( n# e6 h5 |26.[Genetic studies on mental disorders: recent topics on clinical and molecular genetics].
& j/ ?6 @2 h, a3 e6 S, r; V% JSeishin Shinkeigaku Zasshi. 2004;106(12):1604-9. Review. Japanese. No abstract available.
+ I2 H7 ]  w5 |2 l. y& LPMID: 15770964 [PubMed - indexed for MEDLINE]
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29.Analysis of the human VPS13 gene family.Velayos-Baeza A, Vettori A, Copley RR, Dobson-Stone C, Monaco AP.
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$ \, W, u' |, M* M& {% a: P3 B9 `4.The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules.
6 `# {3 ^7 X+ N2 ], Z; \6 y+ MBouyain S, Watkins DJ.Proc Natl Acad Sci U S A. 2010 Feb 9;107(6):2443-8. Epub 2010 Jan 21.0 _# T9 H8 t+ ^) M
PMID: 20133774 [PubMed - indexed for MEDLINE]Free PMC ArticleFree text- K& ^9 t. v; h6 O. |

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5.Neuronal pentraxin receptor in cerebrospinal fluid as a potential biomarker for neurodegenerative diseases.
- Q% C' e5 F3 c% X5 G- vYin GN, Lee HW, Cho JY, Suk K.Brain Res. 2009 Apr 10;1265:158-70. Epub 2009 Feb 6.1 }6 [4 E# ?, {2 I1 v- B- F
PMID: 19368810 [PubMed - indexed for MEDLINE]: n, a! i: ]2 B0 y/ Q

0 |6 D! v: c4 g* m16.The neuronal growth and regeneration associated Cntn1 (F3/F11/Contactin) gene is duplicated in fish: expression during development and retinal axon regeneration.
$ E/ S/ E( d/ `! F/ G7 V2 _3 f  oHaenisch C, Diekmann H, Klinger M, Gennarini G, Kuwada JY, Stuermer CA.' B4 W2 |* z; j
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18.Transgenic mice expressing F3/contactin from the TAG-1 promoter exhibit developmentally regulated changes in the differentiation of cerebellar neurons.
+ ~1 J/ v. y. p2 e* z- FBizzoca A, Virgintino D, Lorusso L, Buttiglione M, Yoshida L, Polizzi A, Tattoli M, Cagiano R, Rossi F, Kozlov S, Furley A, Gennarini G.
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4 ?* b. j; N; y2 W0 @$ W8.MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization.
$ G1 d$ S7 W4 T$ B) xSuzuki M, Hara Y, Takagi C, Yamamoto TS, Ueno N.
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3.IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervous system.$ N$ A* L' }0 b7 H
Ferrante MI, Ghiani M, Bulfone A, Franco B.
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4.Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation.1 ~% w; n) _3 G; h8 j
Jin H, Gardner RJ, Viswesvaraiah R, Muntoni F, Roberts RG.0 r; W9 t7 W; j: ~5 ^" c
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laolifeidao999

15.Rat olfactory bulb and epithelium UDP-glucuronosyltransferase 2A1 (UGT2A1) expression: in situ mRNA localization and quantitative analysis.

laolifeidao999

11.A neuropathological study of autosomal-dominant chorea-acanthocytosis with a mutation of VPS13A.

laolifeidao999

16.Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C.

laolifeidao999

29.Analysis of the human VPS13 gene family.

laolifeidao999

4.The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules.

laolifeidao999

5.Neuronal pentraxin receptor in cerebrospinal fluid as a potential biomarker for neurodegenerative diseases.