Difference between revisions of "Hoatlin Lab"

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{{HoatlinLab}}
 
{{HoatlinLab}}
  
Our lab is interested in understanding how the [http://www.fanconi.org/ Fanconi anemia] proteins contribute to genomic stability with the goal of developing drugs that will help Fanconi patients and those who are susceptible to developing cancer.
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We work in [[Hoatlin:Portland Oregon| Portland, Oregon]] at [http://www.ohsu.edu/ OHSU], in the [http://www.ohsu.edu/biochem/ Department of Biochemistry & Molecular Biology].
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We hope that other Fanconi labs will join us at [http://openwetware.org/wiki/ OpenWetWare] to speed FA research, stimulate collaborative efforts, facilitate reagent distribution, and expand communication. We also believe that an understanding of the complex and enigmatic Fanconi anemia protein network could benefit from the attention of systems/synthetic biologists already on OWW.  
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Please see [http://www.sciam.com/article.cfm?id=science-2-point-0-great-new-tool-or-great-risk link to Scientific American article] now online about OWW and Science 2.0.  
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'''Lab News'''
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;For news, follow the [http://twitter.com/HoatlinLab Hoatlin lab Twitter]
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Our laboratory is interested in understanding the molecular function of the Fanconi anemia (FA) protein network in context with other proteins that regulate or influence genomic stability. Fanconi anemia is a rare genetic disease that is typically associated with developmental abnormalities, bone marrow failure and increased risk of cancer. Because the majority of the FA proteins are unique with no significant homologies, we expect the results of our studies to shed new light on fundamental mechanisms that control the integrity of the human genome and influence cancer susceptibility. The FA pathway is part of a network of proteins that contains BRCA2 and two other recently identified FA genes (FANCN and FANCJ) that influence breast cancer susceptibility. Ultimately, insights into the mechanism of the FA/BRCA network of proteins will lead to an understanding of the underlying molecular defect in FA and may lead to more effective avenues of treatment for this devastating pediatric disease and cancer.  
  
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We work in [[Hoatlin:Portland Oregon| Portland, Oregon]] at [http://www.ohsu.edu/ OHSU], in the [http://www.ohsu.edu/biochem/ Department of Biochemistry & Molecular Biology] and the [http://www.ohsucancer.com/ OHSU Knight Cancer Institute].
  
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==Teaching Links==
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*Our lab's Fanconi Anemia antibodies are available from [http://www.novusbio.com Novus Biologicals] and soon by Millipore.
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[http://openwetware.org/wiki/CANB_610 Advanced Topics in Cancer Biology (CANB 610)]
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[[Hoatlin:OHSU_Genetic_Mechanisms_Class| Genetic Mechanisms Class (CON662)]]
  
==Other Quick Links==
 
 
[[Hoatlin:OHSU Replication, Recombination and Repair (R3) Club| OHSU DNA Replication, Recombination and Repair (R3) Club]].
 
[[Hoatlin:OHSU Replication, Recombination and Repair (R3) Club| OHSU DNA Replication, Recombination and Repair (R3) Club]].
  
[[Hoatlin:BMB Seminar Series '08-'09| BMB Seminar Series for 2008-2009 ]]
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[[Hoatlin: CSF|Med Students Cell Structure Function (CSF)]]
  
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==Classes of the past==
 
[[BMCB625|Advanced Topics in Molecular Biology(BMB625)]]
 
[[BMCB625|Advanced Topics in Molecular Biology(BMB625)]]
 
[[Hoatlin:CON662DNA Replication|CON662 Student Space]]
 
  
 
==Who is Visiting Us?==
 
==Who is Visiting Us?==

Revision as of 18:41, 22 January 2014

Equipped with his five senses, man explores the universe around him and calls the adventure Science.  ~Edwin Powell Hubble, The Nature of Science, 1954

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Lab News

For news, follow the Hoatlin lab Twitter


Our laboratory is interested in understanding the molecular function of the Fanconi anemia (FA) protein network in context with other proteins that regulate or influence genomic stability. Fanconi anemia is a rare genetic disease that is typically associated with developmental abnormalities, bone marrow failure and increased risk of cancer. Because the majority of the FA proteins are unique with no significant homologies, we expect the results of our studies to shed new light on fundamental mechanisms that control the integrity of the human genome and influence cancer susceptibility. The FA pathway is part of a network of proteins that contains BRCA2 and two other recently identified FA genes (FANCN and FANCJ) that influence breast cancer susceptibility. Ultimately, insights into the mechanism of the FA/BRCA network of proteins will lead to an understanding of the underlying molecular defect in FA and may lead to more effective avenues of treatment for this devastating pediatric disease and cancer.

We work in Portland, Oregon at OHSU, in the Department of Biochemistry & Molecular Biology and the OHSU Knight Cancer Institute.

Teaching Links

  • Our lab's Fanconi Anemia antibodies are available from Novus Biologicals and soon by Millipore.

Advanced Topics in Cancer Biology (CANB 610)

Genetic Mechanisms Class (CON662)

OHSU DNA Replication, Recombination and Repair (R3) Club.

Med Students Cell Structure Function (CSF)

Classes of the past

Advanced Topics in Molecular Biology(BMB625)

Who is Visiting Us?

Who's visiting?

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Basic Wiki/OWW Links

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Recent changes

22 October 2017

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[Vishnu Karthigeyan‎; Priscilla Y. Han‎; Adrienne L. Parkinson‎; Jason Zhang‎ (3×)]

     

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BME100 f2017:Group13 W1030 L4‎‎ (7 changes | history) . . (+950). . [Daniel Beltran Salas‎ (7×)]

     

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     19:13 (User creation log) . . User account Peter (talk | contribs) was created by Yar (talk | contribs) and password was sent by email ‎
     18:59  Biomod/2017/StJohns‎ (diff | hist) . . (+291). . Alexkk15 (talk | contribs)
     18:51  User:Vishnu Karthigeyan‎ (diff | hist) . . (+7). . Vishnu Karthigeyan (talk | contribs) (Contact Info)
     18:49  BME100 f2017:Group16 W1030 L4‎ (diff | hist) . . (+1,931). . Hannah Correa (talk | contribs)
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