胡達·佐格比 (Chinese Wikipedia)
Analysis of information sources in references of the Wikipedia article "胡達·佐格比" in Chinese language version.
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amacad.org
- Dr. Huda Y. Zoghbi. 美國文理科學院. [2018-12-04]. （原始内容存档于2018-12-06）.
ashg.org
- 2019 ASHG Award Recipients | ASHG. www.ashg.org. [2019-07-25]. （原始内容存档于2019-07-25）.
bcm.edu
- Huda Yahya Zoghbi, M.D.. 貝勒醫學院. [2018-11-14]. （原始内容存档于2019-04-25）.
breakthroughprize.org
- Breakthrough Prize Life Sciences Laureates 2017. 突破獎基金會. [2018-12-03]. （原始内容存档于2021-04-28）.
doi.org
- Nuzzo, Regina. Profile of Huda Y. Zoghbi. 美國國家科學院院刊. 2006-02-28, 103 (9): 3017–3019. PMC 1413894
. PMID 16492741. doi:10.1073/pnas.0509604103. - Neill, Ushma S. A conversation with Huda Zoghbi. 臨床研究期刊. 2016-03-01, 126 (3): 797–798. PMC 4767342 . PMID 26928032. doi:10.1172/JCI86445.
- Zoghbi, Huda Y.; Percy, Alan K.; Glaze, Daniel G.; Butler, Ian J.; Riccardi, Vincent M. Reduction of Biogenic Amine Levels in the Rett Syndrome. 新英格蘭醫學雜誌. 1985-10-10, 33 (15): 921–924. PMID 2412119. doi:10.1056/NEJM198510103131504.
- Orr, Harry T.; Chung, Ming-yi; Banfi, Sandro; Kwiatkowski Jr., Thomas J.; Servadio, Antonio; Beaudet, Arthur L.; McCall, Alanna E.; Duvick, Lisa A.; Ranum, Laura P. W.; Zoghbi, Huda Y. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. 自然-遺傳學. 1993-07-01, 4 (3): 221–226. PMID 8358429. doi:10.1038/ng0793-221.
- Cummings, Christopher J.; Mancini, Michael A.; Antalffy, Barbara; DeFranco, Donald B.; Orr, Harry T.; Zoghbi, Huda Y. Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1. 自然-遺傳學. 1998-06-01, 19 (2): 148–154. PMID 9620770. doi:10.1038/502.
- Ben-Arie, Nissim; McCall, Alanna E.; Berkman, Scott; Eichele, Gregor; Bellen, Hugo J.; Zoghbi, Huda Y. Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis. 人類分子遺傳學. 1996-09-01, 5 (9): 1207–1216. PMID 8872459. doi:10.1093/hmg/5.9.1207.
- Bermingham, Nessan A.; Hassan, Bassem A.; Price, Steven D.; Vollrath, Melissa A.; Ben-Arie, Nissim; Eatock, Ruth A.; Bellen, Hugo J.; Lysakowski, Anna; Zoghbi, Huda Y. Math1: An Essential Gene for the Generation of Inner Ear Hair Cells. 科學. 1999-06-11, 284 (5421): 1837–1841. PMID 10364557. doi:10.1126/science.284.5421.1837.
- Yang, Qi; Bermingham, Nessan A.; Finegold, Milton J.; Zoghbi, Huda Y. Requirement of Math1 for secretory cell lineage commitment in the mouse intestine. 科學. 2001-12-07, 294 (5549): 2155–2158. PMID 11739954. doi:10.1126/science.1065718.
- Amir, Ruthie E.; Van den Veyver, Ignatia B.; Wan, Mimi; Tran, Charles Q.; Francke, Uta; Zoghbi, Huda Y. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 自然-遺傳學. 1999-10-01, 23 (2): 185–188. PMID 10508514. doi:10.1038/13810.
- Collins, Ann L.; Levenson, Jonathan M.; Vilaythong, Alexander P.; Richman,Ronald; Armstrong, Dawna L.; Noebels, Jeffrey L.; Sweatt, J. David; Zoghbi, Huda Y. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. 人類分子遺傳學. 2004-09-06, 13 (21): 2679–2689. PMID 15351775. doi:10.1093/hmg/ddh282.
- Samaco, Rodney C.; Mandel-Brehm, Caleigh; Chao, Hsiao-Tuan; Ward, Christopher S.; Fyffe-Maricich, Sharyl L.; Ren, Jun; Hyland, Keith; Thaller, Christina; Maricich, Stephen M.; Humphreys, Peter; Greer, John J.; Percy, Alan; Glaze, Daniel G.; Zoghbi, Huda Y.; Neul, Jeffrey L. Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. 美國國家科學院院刊. 2009-12-22, 106 (51): 21966–21971. PMC 2799790 . PMID 20007372. doi:10.1073/pnas.0912257106.
- Chen, Lin; Chen, Kaifu; Lavery, Laura A.; Baker, Steven A.; Shaw, Chad A.; Li, Wei; Zoghbi, Huda Y. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome. 美國國家科學院院刊. 2015-04-28, 112 (17): 5509–5514. PMC 4418849 . PMID 25870282. doi:10.1073/pnas.1505909112.
- Ure, Kerstin; Lu, Hui; Wang, Wei; Ito-Ishida, Aya; Wu, Zhenyu; He, Ling-jie; Sztainberg, Yehezkel; Chen, Wu; Tang, Jianrong; Zoghbi, Huda Y. Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome. eLife. 2016-06-21, 5: e14198. PMC 4946897 . PMID 27328321. doi:10.7554/eLife.14198.
feinsteininstitute.org
- Molecular Medicine awards Ross Prize to Baylor College of Medicine’s Huda Zoghbi (新闻稿). 范恩斯坦醫學研究所. 2018-03-08 [2018-12-03]. （原始内容存档于2019-03-27）.
gairdner.org
- Huda Y Zoghbi. 蓋爾德納基金會. [2018-12-03]. （原始内容存档于2020-08-01）.
houstonmethodist.org
- William A. Zoghbi, MD, FASE, FAHA, MACC. 休斯敦循道醫院. [2018-12-05]. （原始内容存档于2019-06-04）.
jax.org
- Ellen, Elliot. Women in science: Huda Zoghbi discovered the genetic basis of Rett syndrome. 積克遜實驗室. 2018-03-12 [2018-11-17]. （原始内容存档于2018-11-18）.
kavliprize.org
- Kavli Prize 2022. [2023-08-20]. （原始内容存档于2023-04-26）.
lundbeckfonden.com
- The Brain Prize Winners. [2020-04-29]. （原始内容存档于2020-05-13）.
mit.edu
news.mit.edu
- Arab Students' Organization hosts awards. 麻省理工學院. 2007-04-12 [2018-12-03]. （原始内容存档于2021-03-02）.
nasonline.org
- Jessie Stevenson Kovalenko Medal. 美國國家科學院. [2018-12-03]. （原始内容存档于2016-05-27）.
nih.gov
ncbi.nlm.nih.gov
- Nuzzo, Regina. Profile of Huda Y. Zoghbi. 美國國家科學院院刊. 2006-02-28, 103 (9): 3017–3019. PMC 1413894 . PMID 16492741. doi:10.1073/pnas.0509604103.
- Neill, Ushma S. A conversation with Huda Zoghbi. 臨床研究期刊. 2016-03-01, 126 (3): 797–798. PMC 4767342 . PMID 26928032. doi:10.1172/JCI86445.
- Zoghbi, Huda Y.; Percy, Alan K.; Glaze, Daniel G.; Butler, Ian J.; Riccardi, Vincent M. Reduction of Biogenic Amine Levels in the Rett Syndrome. 新英格蘭醫學雜誌. 1985-10-10, 33 (15): 921–924. PMID 2412119. doi:10.1056/NEJM198510103131504.
- Orr, Harry T.; Chung, Ming-yi; Banfi, Sandro; Kwiatkowski Jr., Thomas J.; Servadio, Antonio; Beaudet, Arthur L.; McCall, Alanna E.; Duvick, Lisa A.; Ranum, Laura P. W.; Zoghbi, Huda Y. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. 自然-遺傳學. 1993-07-01, 4 (3): 221–226. PMID 8358429. doi:10.1038/ng0793-221.
- Cummings, Christopher J.; Mancini, Michael A.; Antalffy, Barbara; DeFranco, Donald B.; Orr, Harry T.; Zoghbi, Huda Y. Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1. 自然-遺傳學. 1998-06-01, 19 (2): 148–154. PMID 9620770. doi:10.1038/502.
- Ben-Arie, Nissim; McCall, Alanna E.; Berkman, Scott; Eichele, Gregor; Bellen, Hugo J.; Zoghbi, Huda Y. Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis. 人類分子遺傳學. 1996-09-01, 5 (9): 1207–1216. PMID 8872459. doi:10.1093/hmg/5.9.1207.
- Ben-Arie, Nissim; Bellen, Hugo J.; Armstrong, Dawna L.; McCall, Alanna E.; Gordadze, Polina R.; Guo, Qiuxia; Matzuk, Martin M.; Zoghbi, Huda Y. Math1 is essential for genesis of cerebellar granule neurons. 自然. 1997-11-13, 390 (6656): 169–172. PMID 9367153.
- Bermingham, Nessan A.; Hassan, Bassem A.; Price, Steven D.; Vollrath, Melissa A.; Ben-Arie, Nissim; Eatock, Ruth A.; Bellen, Hugo J.; Lysakowski, Anna; Zoghbi, Huda Y. Math1: An Essential Gene for the Generation of Inner Ear Hair Cells. 科學. 1999-06-11, 284 (5421): 1837–1841. PMID 10364557. doi:10.1126/science.284.5421.1837.
- Yang, Qi; Bermingham, Nessan A.; Finegold, Milton J.; Zoghbi, Huda Y. Requirement of Math1 for secretory cell lineage commitment in the mouse intestine. 科學. 2001-12-07, 294 (5549): 2155–2158. PMID 11739954. doi:10.1126/science.1065718.
- Ellison, Kimberley A.; Fill, Carolyn P.; Terwilliger, Joseph; DeGennaro, Louis J.; Martin-Gallardo, Antonia; Anvret, Maria; Percy, Alan K.; Ott, Jurg; Zoghbi, Huda Y. Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. 美國人類遺傳學期刊. 1992-02, 50 (2): 278–287. PMC 1682446 . PMID 1734712.
- Amir, Ruthie E.; Van den Veyver, Ignatia B.; Wan, Mimi; Tran, Charles Q.; Francke, Uta; Zoghbi, Huda Y. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 自然-遺傳學. 1999-10-01, 23 (2): 185–188. PMID 10508514. doi:10.1038/13810.
- Collins, Ann L.; Levenson, Jonathan M.; Vilaythong, Alexander P.; Richman,Ronald; Armstrong, Dawna L.; Noebels, Jeffrey L.; Sweatt, J. David; Zoghbi, Huda Y. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. 人類分子遺傳學. 2004-09-06, 13 (21): 2679–2689. PMID 15351775. doi:10.1093/hmg/ddh282.
- Samaco, Rodney C.; Mandel-Brehm, Caleigh; Chao, Hsiao-Tuan; Ward, Christopher S.; Fyffe-Maricich, Sharyl L.; Ren, Jun; Hyland, Keith; Thaller, Christina; Maricich, Stephen M.; Humphreys, Peter; Greer, John J.; Percy, Alan; Glaze, Daniel G.; Zoghbi, Huda Y.; Neul, Jeffrey L. Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. 美國國家科學院院刊. 2009-12-22, 106 (51): 21966–21971. PMC 2799790 . PMID 20007372. doi:10.1073/pnas.0912257106.
- Chen, Lin; Chen, Kaifu; Lavery, Laura A.; Baker, Steven A.; Shaw, Chad A.; Li, Wei; Zoghbi, Huda Y. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome. 美國國家科學院院刊. 2015-04-28, 112 (17): 5509–5514. PMC 4418849 . PMID 25870282. doi:10.1073/pnas.1505909112.
- Ure, Kerstin; Lu, Hui; Wang, Wei; Ito-Ishida, Aya; Wu, Zhenyu; He, Ling-jie; Sztainberg, Yehezkel; Chen, Wu; Tang, Jianrong; Zoghbi, Huda Y. Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome. eLife. 2016-06-21, 5: e14198. PMC 4946897 . PMID 27328321. doi:10.7554/eLife.14198.
shawprize.org
- Zoghbi, Huda Y. Autobiography of Huda Y Zoghbi. 邵逸夫獎基金會. 2016-09-27 [2018-11-14]. （原始内容存档于2018-11-19）.
- Biographical Notes of Laureates. 邵逸夫獎基金會. 2016-05-31 [2018-12-06]. （原始内容存档于2018-12-09）.
texaschildrens.org
nri.texaschildrens.org
- Dr. Huda Zoghbi receives Lebanon's highest honor. 珍·鄧肯與丹·鄧肯神經內科研究所. 2018-01-23 [2018-12-03]. （原始内容存档于2020-10-25）.
the-scientist.com
- Azvolinsky, Anna. Genetic Neurologist: A Profile of Huda Zoghbi. 科學人. 2018-11-01 [2018-11-17]. （原始内容存档于2019-12-17）.
tmc.edu
digitalcommons.library.tmc.edu
- Zoghbi, Huda. Interview with Huda Zoghbi. 访谈 with McMullen Darra. 德州醫學中心女性科學家歷史計劃. 2016-02-09 [2018-11-23]. （原始内容存档于2020-06-03）.
washingtonpost.com
- Cha, Ariana Eunjung. Silicon Valley’s ‘Nobels’: Mega-prizes awarded for work in brains, the origins of life and gravitational waves. 華盛頓郵報. 2016-12-04 [2018-11-14]. （原始内容存档于2018-10-15）.
web.archive.org
- Huda Y. Zoghbi, M.D.. 再生製藥. [2018-11-25]. （原始内容存档于2019-02-23）.
- Cha, Ariana Eunjung. Silicon Valley’s ‘Nobels’: Mega-prizes awarded for work in brains, the origins of life and gravitational waves. 華盛頓郵報. 2016-12-04 [2018-11-14]. （原始内容存档于2018-10-15）.
- Azvolinsky, Anna. Genetic Neurologist: A Profile of Huda Zoghbi. 科學人. 2018-11-01 [2018-11-17]. （原始内容存档于2019-12-17）.
- Zoghbi, Huda Y. Autobiography of Huda Y Zoghbi. 邵逸夫獎基金會. 2016-09-27 [2018-11-14]. （原始内容存档于2018-11-19）.
- Huda Yahya Zoghbi, M.D.. 貝勒醫學院. [2018-11-14]. （原始内容存档于2019-04-25）.
- Ellen, Elliot. Women in science: Huda Zoghbi discovered the genetic basis of Rett syndrome. 積克遜實驗室. 2018-03-12 [2018-11-17]. （原始内容存档于2018-11-18）.
- Zoghbi, Huda. Interview with Huda Zoghbi. 访谈 with McMullen Darra. 德州醫學中心女性科學家歷史計劃. 2016-02-09 [2018-11-23]. （原始内容存档于2020-06-03）.
- Biographical Notes of Laureates. 邵逸夫獎基金會. 2016-05-31 [2018-12-06]. （原始内容存档于2018-12-09）.
- Huda Yahya Zoghbi. 虛擬綜合臨床及轉移研究中心. [2018-12-04]. （原始内容存档于2020-10-21）.
- Arab Students' Organization hosts awards. 麻省理工學院. 2007-04-12 [2018-12-03]. （原始内容存档于2021-03-02）.
- Jessie Stevenson Kovalenko Medal. 美國國家科學院. [2018-12-03]. （原始内容存档于2016-05-27）.
- Huda Y Zoghbi. 蓋爾德納基金會. [2018-12-03]. （原始内容存档于2020-08-01）.
- Breakthrough Prize Life Sciences Laureates 2017. 突破獎基金會. [2018-12-03]. （原始内容存档于2021-04-28）.
- Dr. Huda Zoghbi receives Lebanon's highest honor. 珍·鄧肯與丹·鄧肯神經內科研究所. 2018-01-23 [2018-12-03]. （原始内容存档于2020-10-25）.
- Molecular Medicine awards Ross Prize to Baylor College of Medicine’s Huda Zoghbi (新闻稿). 范恩斯坦醫學研究所. 2018-03-08 [2018-12-03]. （原始内容存档于2019-03-27）.
- Dr. Huda Y. Zoghbi. 美國文理科學院. [2018-12-04]. （原始内容存档于2018-12-06）.
- 2019 ASHG Award Recipients | ASHG. www.ashg.org. [2019-07-25]. （原始内容存档于2019-07-25）.
- The Brain Prize Winners. [2020-04-29]. （原始内容存档于2020-05-13）.
- Kavli Prize 2022. [2023-08-20]. （原始内容存档于2023-04-26）.
- William A. Zoghbi, MD, FASE, FAHA, MACC. 休斯敦循道醫院. [2018-12-05]. （原始内容存档于2019-06-04）.
wikipedia.org
en.wikipedia.org
- Huda Y. Zoghbi, M.D.. 再生製藥. [2018-11-25]. （原始内容存档于2019-02-23）.
- Ellen, Elliot. Women in science: Huda Zoghbi discovered the genetic basis of Rett syndrome. 積克遜實驗室. 2018-03-12 [2018-11-17]. （原始内容存档于2018-11-18）.
- Neill, Ushma S. A conversation with Huda Zoghbi. 臨床研究期刊. 2016-03-01, 126 (3): 797–798. PMC 4767342 . PMID 26928032. doi:10.1172/JCI86445.
- Zoghbi, Huda. Interview with Huda Zoghbi. 访谈 with McMullen Darra. 德州醫學中心女性科學家歷史計劃. 2016-02-09 [2018-11-23]. （原始内容存档于2020-06-03）.
- Ben-Arie, Nissim; McCall, Alanna E.; Berkman, Scott; Eichele, Gregor; Bellen, Hugo J.; Zoghbi, Huda Y. Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis. 人類分子遺傳學. 1996-09-01, 5 (9): 1207–1216. PMID 8872459. doi:10.1093/hmg/5.9.1207.
- Ellison, Kimberley A.; Fill, Carolyn P.; Terwilliger, Joseph; DeGennaro, Louis J.; Martin-Gallardo, Antonia; Anvret, Maria; Percy, Alan K.; Ott, Jurg; Zoghbi, Huda Y. Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. 美國人類遺傳學期刊. 1992-02, 50 (2): 278–287. PMC 1682446 . PMID 1734712.
- Molecular Medicine awards Ross Prize to Baylor College of Medicine’s Huda Zoghbi (新闻稿). 范恩斯坦醫學研究所. 2018-03-08 [2018-12-03]. （原始内容存档于2019-03-27）.
- William A. Zoghbi, MD, FASE, FAHA, MACC. 休斯敦循道醫院. [2018-12-05]. （原始内容存档于2019-06-04）.