User:Eva Klinman: Difference between revisions
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==Contact Info== | ==Contact Info== | ||
[[Image:Photo 54.jpg|thumb|right|Eva Klinman's puppy]] | [[Image:Photo 54.jpg|thumb|right|Eva Klinman's puppy]] | ||
*Eva Klinman | *Eva Klinman | ||
*MIT, | *MIT, Senior | ||
*Room | *Room 370, Next House | ||
*Home Address: Potomac MD | *Home Address: Potomac MD | ||
*[[Special:Emailuser/Eva Klinman|Email me through OpenWetWare]] | *[[Special:Emailuser/Eva Klinman|Email me through OpenWetWare]] | ||
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===Related Classes=== | ===Related Classes=== | ||
[[Classes]] | |||
===Lab Work=== | ===Lab Work=== | ||
For three years, I worked at NIH, in the NICHD. I took part in the research being conducted in the lab of Dr. Brant Weinstein, working with vascular morphogenesis in embryonic zebrafish. | For three years, I worked at NIH, in the NICHD. I took part in the research being conducted in the lab of Dr. [http://uvo.nichd.nih.gov/ Brant Weinstein], working with vascular morphogenesis in embryonic zebrafish. | ||
From Jan 2008-Jan 2009, I worked with Dr. Andreas Herrlich in the [http://web.wi.mit.edu/lodish/pub/research/r_overview.html Lodish lab] at the Whitehead. We performed a large-scale high-throughput screen to test the effects a set of shRNAs designed to knock-down most human kinases and phophatases has on ectodomain cleavage. Specifically, we used osmotic stress as a cleavage stimulus to the EGF ligand TGF-alpha. We worked in human Jurkat cells, and mouse Baf3 cell lines. | |||
[http://openwetware.org/wiki/Herpes_Simplex_Virus_%28HSV_I%29_as_Cancer_Targeting_Agent Previous 20.109 labwork] | |||
Currently, I work in the lab of Dr. [http://edboyden.org/ Ed Boyden]. I am involved in the Epilepsy research group, an attempt to cause and then silence seizure activity in mice using optically controlled neurons. Over the summer, I am also working with the molecular biology group, to clone multiple new mutants of rhodopsins into usable backbones, which will then be used to generate virus capable of infecting neurons and introducing light-sensitive ion channels. | |||
==Personal Info== | |||
=== | ===Meet: Me=== | ||
I am familiar with lab environments and tissue culture set-up and usage. | I am familiar with lab environments and tissue culture set-up and usage. | ||
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===Outside Activities=== | ===Outside Activities=== | ||
* Dance Troupe | * [http://dancetroupe.mit.edu/ Dance Troupe] | ||
* Next Act | * [http://mit.edu/nextact/index.htm Next Act] | ||
* UROP | * UROP | ||
* [http://web.mit.edu/murj/www/index16.html MURJ (MIT Undergraduate Research Journal)] | |||
==Useful links== | ==Useful links== | ||
*[[OpenWetWare:Welcome|Introductory tutorial]] | *[[OpenWetWare:Welcome|Introductory tutorial]] | ||
*[[Help|OpenWetWare help pages]] | *[[Help|OpenWetWare help pages]] |
Latest revision as of 13:43, 9 July 2009
Contact Info
- Eva Klinman
- MIT, Senior
- Room 370, Next House
- Home Address: Potomac MD
- Email me through OpenWetWare
Education
- 2006, Winston Churchill High School
- 2010, MIT: Biological Engineering, focus in Neuroscience
Research interests
- Neurons
- Alzheimer's disease
- microRNA
Classes and Research
Course/Minor
Minor: course 9, Neuroscience
Year of Graduation
2010
eklinman AT mit DOT edu
Related Classes
Lab Work
For three years, I worked at NIH, in the NICHD. I took part in the research being conducted in the lab of Dr. Brant Weinstein, working with vascular morphogenesis in embryonic zebrafish.
From Jan 2008-Jan 2009, I worked with Dr. Andreas Herrlich in the Lodish lab at the Whitehead. We performed a large-scale high-throughput screen to test the effects a set of shRNAs designed to knock-down most human kinases and phophatases has on ectodomain cleavage. Specifically, we used osmotic stress as a cleavage stimulus to the EGF ligand TGF-alpha. We worked in human Jurkat cells, and mouse Baf3 cell lines.
Currently, I work in the lab of Dr. Ed Boyden. I am involved in the Epilepsy research group, an attempt to cause and then silence seizure activity in mice using optically controlled neurons. Over the summer, I am also working with the molecular biology group, to clone multiple new mutants of rhodopsins into usable backbones, which will then be used to generate virus capable of infecting neurons and introducing light-sensitive ion channels.
Personal Info
Meet: Me
I am familiar with lab environments and tissue culture set-up and usage.
I am a very active person, and tend to dance often, and sing or hum without realizing it. If it causes others around me to get annoyed, please make me aware of what I'm doing and ask me to stop!