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Items: 23

1.

Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy.

Tian WT, Zhan FX, Liu Q, Luan XH, Zhang C, Shang L, Zhang BY, Pan SJ, Miao F, Hu J, Zhong P, Liu SH, Zhu ZY, Zhou HY, Sun S, Liu XL, Huang XJ, Jiang JW, Ma JF, Wang Y, Chen SF, Tang HD, Chen SD, Cao L.

Transl Neurodegener. 2019 Dec 2;8:32. doi: 10.1186/s40035-019-0171-y. eCollection 2019.

2.

Primary familial brain calcification presenting as paroxysmal kinesigenic dyskinesia: Genetic and functional analyses.

Zhan FX, Tian WT, Zhang C, Zhu ZY, Wang SG, Huang XJ, Cao L.

Neurosci Lett. 2020 Jan 1;714:134543. doi: 10.1016/j.neulet.2019.134543. Epub 2019 Oct 13.

PMID:
31618668
3.

Lysosomal degradation of GMPPB is associated with limb-girdle muscular dystrophy type 2T.

Tian WT, Zhou HY, Zhan FX, Zhu ZY, Yang J, Chen SD, Luan XH, Cao L.

Ann Clin Transl Neurol. 2019 May 8;6(6):1062-1071. doi: 10.1002/acn3.787. eCollection 2019 Jun.

4.

Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review.

Tian WT, Luan XH, Zhou HY, Zhang C, Huang XJ, Liu XL, Chen SD, Tang HD, Cao L.

Neuromuscul Disord. 2019 Apr;29(4):282-289. doi: 10.1016/j.nmd.2019.01.001. Epub 2019 Jan 6.

PMID:
30737079
5.

Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders.

Zhang C, Zhan FX, Tian WT, Xu YQ, Zhu ZY, Wang Y, Song XW, Cao L.

Clin Neurol Neurosurg. 2019 Feb;177:92-96. doi: 10.1016/j.clineuro.2019.01.004. Epub 2019 Jan 7.

PMID:
30640048
6.

The study of exercise tests in paroxysmal kinesigenic dyskinesia.

Zhou HY, Zhan FX, Tian WT, Zhang C, Wang Y, Zhu ZY, Liu XL, Xu YQ, Luan XH, Huang XJ, Chen SD, Cao L.

Clin Neurophysiol. 2018 Nov;129(11):2435-2441. doi: 10.1016/j.clinph.2018.09.004. Epub 2018 Sep 15.

PMID:
30293034
7.

Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review.

Tian WT, Liu XL, Xu YQ, Huang XJ, Zhou HY, Wang Y, Tang HD, Chen SD, Luan XH, Cao L.

Seizure. 2018 Apr;57:80-86. doi: 10.1016/j.seizure.2018.03.015. Epub 2018 Mar 14. Review.

8.

Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis.

Xu YQ, Liu XL, Huang XJ, Tian WT, Tang HD, Cao L.

Chin Med J (Engl). 2018 Feb 20;131(4):477-479. doi: 10.4103/0366-6999.225061. No abstract available.

9.

Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.

Tian WT, Huang XJ, Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L.

Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. Epub 2018 Jan 22.

PMID:
29356177
10.

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS.

Hum Mol Genet. 2018 Feb 15;27(4):757-758. doi: 10.1093/hmg/ddy025. No abstract available.

PMID:
29351621
11.

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS.

Hum Mol Genet. 2018 Feb 15;27(4):625-637. doi: 10.1093/hmg/ddx430. Erratum in: Hum Mol Genet. 2018 Feb 15;27(4):757-758.

PMID:
29294000
12.

Bispecific Antibody Binding To RANKL and Osteonectin with Enhanced Localization to the Bone.

Chen JH, Lin CY, Chen YM, Tian WT, Chu HM, Chang TW.

Mol Pharm. 2017 Nov 6;14(11):4113-4120. doi: 10.1021/acs.molpharmaceut.7b00501. Epub 2017 Oct 9.

PMID:
28954509
13.

Depression, anxiety, and quality of life in paroxysmal kinesigenic dyskinesia patients.

Tian WT, Huang XJ, Liu XL, Shen JY, Liang GL, Zhu CX, Tang WG, Chen SD, Song YY, Cao L.

Chin Med J (Engl). 2017 Sep 5;130(17):2088-2094. doi: 10.4103/0366-6999.213431.

14.

Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18.

Tian WT, Shen JY, Liu XL, Wang T, Luan XH, Zhou HY, Chen SD, Huang XJ, Cao L.

Chin Med J (Engl). 2016 Nov 20;129(22):2759-2761. doi: 10.4103/0366-6999.193444. No abstract available.

15.

Influence of spiral framework on nonlinear optical materials.

Hu YY, Sun SL, Tian WT, Tian WQ, Xu HL, Su ZM.

Chemphyschem. 2014 Apr 4;15(5):929-34. doi: 10.1002/cphc.201301149. Epub 2014 Feb 13.

PMID:
24677788
16.

Targeting the XIAP/caspase-7 complex selectively kills caspase-3-deficient malignancies.

Lin YF, Lai TC, Chang CK, Chen CL, Huang MS, Yang CJ, Liu HG, Dong JJ, Chou YA, Teng KH, Chen SH, Tian WT, Jan YH, Hsiao M, Liang PH.

J Clin Invest. 2013 Sep;123(9):3861-75. doi: 10.1172/JCI67951. Epub 2013 Aug 27.

17.

Essential role of β-human 8-oxoguanine DNA glycosylase 1 in mitochondrial oxidative DNA repair.

Su YH, Lee YL, Chen SF, Lee YP, Hsieh YH, Tsai JH, Hsu JL, Tian WT, Huang W.

Environ Mol Mutagen. 2013 Jan;54(1):54-64. doi: 10.1002/em.21742. Epub 2012 Oct 11.

PMID:
23055259
18.

Monoclonal antibodies to T cell receptor gamma/delta complex react with human endometrial glandular epithelium.

Yeh CJ, Bulmer JN, Hsi BL, Tian WT, Rittershaus C, Ip SH.

Placenta. 1990 May-Jun;11(3):253-61.

PMID:
2142527
19.

A study of the immunofunction in patients of coronary heart disease with the fundamental deficiency and outward excess syndrome.

He W, Zhang DS, Wang GS, Li ZQ, Bao FZ, Jin HY, Long ZZ, Ma SJ, Tian WT.

J Tradit Chin Med. 1989 Dec;9(4):290-3.

PMID:
2630821
20.

Two distinct immunogenic epitopes on the alpha chain of human T cell antigen receptor.

Henry L, Tian WT, Rittershaus C, Ko JL, Marsh HC Jr, Ip SH.

Hybridoma. 1989 Dec;8(6):577-88.

PMID:
2482248
21.

Studies on peripheral T lymphocyte subsets in patients with autoimmune thyroid diseases.

Chen G, Zhang KZ, Liao ZH, Wang SH, Ma SJ, Long ZZ, Tian WT, Zhu JY.

Chin Med J (Engl). 1989 Sep;102(9):698-701.

PMID:
2534289
22.

The expression of T cell receptor-associated proteins during T cell ontogeny in man.

Campana D, Janossy G, Coustan-Smith E, Amlot PL, Tian WT, Ip S, Wong L.

J Immunol. 1989 Jan 1;142(1):57-66.

PMID:
2783327
23.

Signal transduction of gamma/delta T cell antigen receptor with a novel mitogenic anti-delta antibody.

Wu YJ, Tian WT, Snider RM, Rittershaus C, Rogers P, LaManna L, Ip SH.

J Immunol. 1988 Sep 1;141(5):1476-9.

PMID:
3261750

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