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分子與基因醫學研究所
江運金
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江運金(Yun-Jin Jiang)
ORCID:0000-0003-0499-7306
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期刊論文
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會議論文/會議摘要
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鄰近社群
劉淦光(2006-2014)
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劉鴻興
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喻秋華
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孫以瀚
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張仲明
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張明姿
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張雅媗
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徐唯哲
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徐欣伶
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施修明
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松浦功
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梁啟銘(2006-2007)
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王紹文
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/15]
王陸海
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/36]
莊志立
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32
/38]
蔡世峯
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134
/147]
許惠恒
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40
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陳俊宏
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陳怡榮
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黃秀芬
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黃麗蓉
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/27]
龔行健
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其他
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/163]
周玉山(1996-2005)
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20
/22]
王玲美(2004-2008)
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/4]
葉秀慧(2001-2005)
[
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/22]
鄭金松(1997-2002)
[
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/6]
黃奇英(1998-2005)
[
32
/34]
社群統計
近3年內發表的文件:4(11.76%)
含全文筆數:34(100.00%)
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最後更新時間: 2025-04-04 02:22
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Fgf8 contributes to the pathogenesi...
p53 inhibitor or antioxidants reduc...
The prolyl isomerase Pin1 stabilize...
Micro-CT analysis reveals the chang...
Genome-wide analysis identified nov...
Delta/Jagged-mediated Notch signali...
Phenotype variability in the patien...
Does Nicastrin inadequacy cause mel...
Newly identified Gon4l/Udu-interact...
Nicastrin deficiency induces tyrosi...
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顯示項目1-25 / 34. (共2頁)
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日期
題名
關聯
2024-11
Fgf8 contributes to the pathogenesis of Nager syndrome
International Journal of Biological Macromolecules. 2024 Nov;280(Part 3):Article number 135692.
2024-05
p53 inhibitor or antioxidants reduce the severity of ethmoid plate deformities in zebrafish type 3 treacher collins syndrome model
International Journal of Biological Macromolecules. 2024 May;266(Part. 2):Article number 131216.
2023-09-18
The prolyl isomerase Pin1 stabilizes NeuroD during differentiation of mechanoreceptors
Frontiers in Cell and Developmental Biology. 2023 Sep 18;11:Article number 1225128.
2023-03
Micro-CT analysis reveals the changes in bone mineral density in zebrafish craniofacial skeleton with age
Journal of Anatomy. 2023 Mar;242(3):544-551.
2022-03-29
Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs
Journal of Headache and Pain. 2022 Mar 29;23:Article number 39.
2021-12-28
Delta/Jagged-mediated Notch signaling induces the differentiation of agr2-positive epidermal mucous cells in zebrafish embryos
PLoS Genetics. 2021 Dec 28;17(12):Article number e1009969.
2021-12
Phenotype variability in the patients of familial exudative vitreoretinopathy: The RCBTB1 case
Current Eye Research. 2021 Dec;46(12):1931.
2021-05
Does Nicastrin inadequacy cause melanocytotoxicity in human skin as in the fish counterpart?
Journal of Investigative Dermatology. 2021 May;141(5):1334-1338.
2020-08-26
Newly identified Gon4l/Udu-interacting proteins implicate novel functions
Scientific Reports. 2020 Aug 26;10:Article number 14213.
2020-02
Nicastrin deficiency induces tyrosinase-dependent depigmentation and skin inflammation
Journal of Investigative Dermatology. 2020 Feb;140(2):404-414.e13.
2019-08-15
Sun1 mediates interkinetic nuclear migration and Notch signaling in the neurogenesis of zebrafish
Stem Cells and Development. 2019 Aug 15;28(16):1116-1127.
2018-02
Comparative transcriptomic characterization of a new mib mutant allele, mibnn2002, in zebrafish
Gene. 2018 Feb;642:51-57.
2018-02
Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
American Journal of Pathology. 2018 Feb;188(2):336-342.
2017-12
Aberrant global and Jagged-mediated Notch signaling disrupts segregation between wt1-expressing and steroidogenic tissues in zebrafish
Endocrinology. 2017 Dec;158(12):4206-4217.
2017-09-05
Epstein-Barr virus BRLF1 induces genomic instability and progressive malignancy in nasopharyngeal carcinoma cells
Oncotarget. 2017 Sep 5;8(45):78948-78964.
2017-07
Zranb1b and Mib1 regulate zebrafish convergent extension through Ryk-mediated non-canonical Wnt signalling
Mechanisms of Development. 2017 Jul;145(Suppl. ):Abstract number S61.
2017-07
Zebrafish nicastrin deficiency leads to a Tyrosinase-dependent depigmentation
Mechanisms of Development. 2017 Jul;145(Suppl.):S99.
2016-09-02
Morphology and gene expression screening with morpholinos in zebrafish embryos
Methods in Molecular Biology. 2016 Sep 02;1470:213-224.
2016-06-06
A sketch of the Taiwan zebrafish core facility, TZCF
Zebrafish. 2016 Jun 6;13(Suppl. 1):S24-S29.
2016-06
Pathogenesis of POLR1C-dependent type 3 treacher collins syndrome revealed by a zebrafish model
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2016 Jun;1862(6):1147-1158.
2016-04
Haploinsufficiency of RCBTB1 is associated with coats disease and familial exudative vitreoretinopathy
Human Molecular Genetics. 2016 Apr;25(8):1637-1647.
2015-12-30
Deltex1 is inhibited by the notch-hairy/E(Spl) signaling pathway and induces neuronal and glial differentiation
Neural Development. 2015 Dec 30;10:Article number 28.
2015-06-03
A new mib allele with a chromosomal deletion covering foxc1a exhibits anterior somite specification defect
Scientific Reports. 2015 Jun 3;5:Article number 10673.
2014-07
Different combinations of Notch ligands and receptors regulate V2 interneuron progenitor proliferation and V2a/V2b cell fate determination
Developmental Biology. 2014 Jul;391(2):196-206.
2014-07
Nicastrin is required for zebrafish pigment and brain development
Alzheimer's and Dementia. 2014 Jul;10(4, Suppl.):P786.
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