Louis Martens Kunkel

Louis Martens Kunkel, Ph.D.

Professor of Genetics and Pediatrics, Harvard Medical School

Director, Genomics Program

617-355-7576

Kunkel Lab Website

Publications

Introduction for: frontiers of personalized cancer medicine.

Authors: Authors: Kucherlapati R.
Cancer J 2011-01-01
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Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation.

Authors: Authors: Chen PC, Wakimoto H, Conner D, Araki T, Yuan T, Roberts A, Seidman C, Bronson R, Neel B, Seidman JG, Kucherlapati R.
J Clin Invest 2010-12-01
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Cathepsin B expression and survival in colon cancer: implications for molecular detection of neoplasia.

Authors: Authors: Chan AT, Baba Y, Shima K, Nosho K, Chung DC, Hung KE, Mahmood U, Madden K, Poss K, Ranieri A, Shue D, Kucherlapati R, Fuchs CS, Ogino S.
Cancer Epidemiol Biomarkers Prev 2010-11-01
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Personalized medicine for non-small-cell lung cancer.

Authors: Authors: Kucherlapati R.
Oncology (Williston Park) 2010-04-30
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In vivo wide-area cellular imaging by side-view endomicroscopy.

Authors: Authors: Kim P, Chung E, Yamashita H, Hung KE, Mizoguchi A, Kucherlapati R, Fukumura D, Jain RK, Yun SH.
Nat Methods 2010-04-01
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Cis lethal genetic interactions attenuate and alter p53 tumorigenesis.

Authors: Authors: Wang Y, Zhang W, Edelmann L, Kolodner RD, Kucherlapati R, Edelmann W.
Proc Natl Acad Sci U S A 2010-03-23
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An Msh2 conditional knockout mouse for studying intestinal cancer and testing anticancer agents.

Authors: Authors: Kucherlapati MH, Lee K, Nguyen AA, Clark AB, Hou H, Rosulek A, Li H, Yang K, Fan K, Lipkin M, Bronson RT, Jelicks L, Kunkel TA, Kucherlapati R, Edelmann W.
Gastroenterology 2010-03-01
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A suggested role for mitochondria in Noonan syndrome.

Authors: Authors: Lee I, Pecinova A, Pecina P, Neel BG, Araki T, Kucherlapati R, Roberts AE, Hüttemann M.
Biochim Biophys Acta 2010-02-01
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Development of a mouse model for sporadic and metastatic colon tumors and its use in assessing drug treatment.

Authors: Authors: Hung KE, Maricevich MA, Richard LG, Chen WY, Richardson MP, Kunin A, Bronson RT, Mahmood U, Kucherlapati R.
Proc Natl Acad Sci U S A 2010-01-26
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A restricted spectrum of NRAS mutations causes Noonan syndrome.

Authors: Authors: Cirstea IC, Kutsche K, Dvorsky R, Gremer L, Carta C, Horn D, Roberts AE, Lepri F, Merbitz-Zahradnik T, König R, Kratz CP, Pantaleoni F, Dentici ML, Joshi VA, Kucherlapati RS, Mazzanti L, Mundlos S, Patton MA, Silengo MC, Rossi C, Zampino G, Digilio C, Stuppia L, Seemanova E, Pennacchio LA, Gelb BD, Dallapiccola B, Wittinghofer A, Ahmadian MR, Tartaglia M, Zenker M.
Nat Genet 2010-01-01
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