Bilaketaren emaitzak - Caroline Andrews
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Interleukin-27 as a Novel Therapy for Inflammatory Bowel Disease nork Caroline Andrews, Mairi H McLean, Scott K. Durum
Argitaratua 2016Revisão -
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Cytokine Tuning of Intestinal Epithelial Function nork Caroline Andrews, Mairi H McLean, Scott K. Durum
Argitaratua 2018Revisão -
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Evidence for a Dual Mechanism for IL-10 Suppression of TNF-α Production That Does Not Involve Inhibition of p38 Mitogen-Activated Protein Kinase or NF-κB in Primary Human Macrophag... nork A Denys, Irina A. Udalova, Clive Smith, Lynn Williams, Cathleen J. Ciesielski, Jamie I. D. Campbell, Caroline Andrews, Dominic Kwaitkowski, Brian M. J. Foxwell
Argitaratua 2002Artigo -
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Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation nork Shery Thomas, Mervyn G. Thomas, Caroline Andrews, Wai‐Man Chan, Frank A. Proudlock, Rebecca J. McLean, Archana Pradeep, Elizabeth C. Engle, Irène Gottlob
Argitaratua 2013Artigo -
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Duane Radial Ray Syndrome (Okihiro Syndrome) Maps to 20q13 and Results from Mutations in SALL4, a New Member of the SAL Family nork Raidah Albaradie, Koki Yamada, Cynthia St. Hilaire, Wai‐Man Chan, Caroline Andrews, Nathalie McIntosh, Motoi Nakano, E. Jean Martonyi, William R. Raymond, Sada Okumura, Michael M. Okihiro, Elizabeth C. Engle
Argitaratua 2002Artigo -
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Two unique <i>TUBB3</i> mutations cause both CFEOM3 and malformations of cortical development nork Mary C. Whitman, Caroline Andrews, Wai‐Man Chan, Max A. Tischfield, Steven F. Stasheff, Francesco Brancati, Xilma R. Ortiz‐González, Sara Nuovo, Francesco Garaci, Sarah MacKinnon, David G. Hunter, P. Ellen Grant, Elizabeth C. Engle
Argitaratua 2015Artigo -
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An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation nork G. Cederquist, Anna Łuchniak, Max A. Tischfield, Maya Peeva, Yuyu Song, Manoj P. Menezes, Wai‐Man Chan, Caroline Andrews, Sheena Chew, Robyn V. Jamieson, Lavier Gomes, Maree Flaherty, P. Ellen Grant, Mohan L. Gupta, Elizabeth C. Engle
Argitaratua 2012Artigo -
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Surface-fill hydrogel attenuates the oncogenic signature of complex anatomical surface cancer in a single application nork Poulami Majumder, Anand Singh, Ziqiu Wang, Kingshuk Dutta, Roma Pahwa, Liang Chen, Caroline Andrews, Nimit L. Patel, Junfeng Shi, Natalia de Val, Scott T.R. Walsh, Albert B. Jeon, Baktiar Karim, Chuong D. Hoang, Joel P. Schneider
Argitaratua 2021Artigo -
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Tumour-elicited neutrophils engage mitochondrial metabolism to circumvent nutrient limitations and maintain immune suppression nork Christopher M. Rice, Luke C. Davies, Jeffrey Subleski, Nunziata Maio, Marieli Gonzalez-Cotto, Caroline Andrews, Nimit L. Patel, Erika M. Palmieri, Jonathan M. Weiss, Jungmin Lee, Christina M. Annunziata, Tracey A. Rouault, Scott K. Durum, Daniel W. McVicar
Argitaratua 2018Artigo -
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HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice nork Bryn D. Webb, Sherin Shaaban, Harald Gaspar, Luis F. Cunha, Christian Schubert, Ke Hao, Caroline D. Robson, Wai‐Man Chan, Caroline Andrews, Sarah MacKinnon, Darren T. Oystreck, David G. Hunter, Anthony J. Iacovelli, Xiaoqian Ye, Anne Camminady, Elizabeth C. Engle, Ethylin Wang Jabs
Argitaratua 2012Artigo -
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A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3 nork Sheena Chew, Ravikumar Balasubramanian, Wai‐Man Chan, Peter B. Kang, Caroline Andrews, Bryn D. Webb, Sarah MacKinnon, Darren T. Oystreck, Jessica K. Rankin, Thomas O. Crawford, Michael T. Geraghty, Scott L. Pomeroy, William F. Crowley, Ethylin Wang Jabs, David G. Hunter, P. Ellen Grant, Elizabeth C. Engle
Argitaratua 2013Artigo -
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Identification of<i>KIF21A</i>Mutations as a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 (CFEOM3) nork Koki Yamada, Wai‐Man Chan, Caroline Andrews, Thomas M. Bosley, Emin Cumhur Şener, Johan T. Zwaan, Paul B. Mullaney, Banu T. O ̈ztu ̈rk, Nurten Akarsu, Louise J. Sabol, Joseph L. Demer, Timothy J. Sullivan, Irène Gottlob, Peter Roggenka ̈emper, David A. Mackey, Clara E. de Uzcátegui, Nicolas Uzcategui, Bruria Ben‐Zeev, Elias I. Traboulsi, Adriano Magli, Teresa de Berardinis, Vincenzo Gagliardi, Sudha Awasthi-Patney, Marlene Vogel, Joseph F. Rizzo, Elizabeth C. Engle
Argitaratua 2004Artigo -
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Mutations in a Human <i>ROBO</i> Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis nork Joanna C. Jen, Wai‐Man Chan, Thomas M. Bosley, Jijun Wan, Janai R. Carr, Udo Rüb, David W. Shattuck, Georges Salamon, Lili C. Kudo, Jing Ou, Doris Lin, Mustafa A. Salih, Tülay Kansu, Hesham al Dhalaan, Zayed Al Zayed, David B. MacDonald, B. Stigsby, Andreas Plaitakis, E. K. Dretakis, Irène Gottlob, Christina Pieh, Elias I. Traboulsi, Qing Wang, Lejin Wang, Caroline Andrews, Koki Yamada, Joseph L. Demer, Shaheen Karim, Jeffry R. Alger, Daniel H. Geschwind, Thomas Deller, Nancy L. Sicotte, Stanley F. Nelson, Robert W. Baloh, Elizabeth C. Engle
Argitaratua 2004Artigo -
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Validation of a multi-ancestry polygenic risk score and age-specific risks of prostate cancer: A meta-analysis within diverse populations nork Fei Chen, Burcu F. Darst, Ravi Madduri, Alex A. Rodríguez, Xin Sheng, Christopher T. Rentsch, Caroline Andrews, Wei Tang, Adam S. Kibel, Anna Plym, Kelly Cho, Mohamed Jalloh, Sérigne Maguèye Gueye, Lamine Niang, Olufemi J. Ogunbiyi, Olufemi Popoola, Akindele O. Adebiyi, Oseremen I. Aisuodionoe-Shadrach, Hafees O. Ajibola, Mustapha A. Jamda, Olabode P. Oluwole, Maxwell M. Nwegbu, Ben Adusei, Sunny Mante, Afua O.D. Abrahams, James E. Mensah, Andrew A. Adjei, Halimatou Diop‐Ndiaye, Joseph Lachance, Timothy R. Rebbeck, Stefan Ambs, J. Michael Gaziano, Amy C. Justice, David V. Conti, Christopher A. Haiman
Argitaratua 2022Revisão -
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Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance nork Max A. Tischfield, Hagit Baris, Chen Wu, Guenther Rudolph, Lionel Van Maldergem, Wei He, Wai‐Man Chan, Caroline Andrews, Joseph L. Demer, Richard L. Robertson, David A. Mackey, Jonathan B. Ruddle, Thomas D. Bird, Irène Gottlob, Christina Pieh, Elias I. Traboulsi, Scott L. Pomeroy, David G. Hunter, Janet S. Soul, Anna Newlin, Louise J. Sabol, Edward J. Doherty, Clara E. de Uzcátegui, Nicolas Uzcategui, Mary Louise Z. Collins, Emin Cumhur Şener, Bettina Wabbels, Heide Hellebrand, Thomas Meitinger, Teresa de Berardinis, Adriano Magli, Costantino Schiavi, Marco Pastore-Trossello, Feray Koc, Agnes Wong, Alex V. Levin, Michael T. Geraghty, Maria Descartes, Maree Flaherty, Robyn V. Jamieson, Hans Ulrik Møller, I. Meuthen, David F. Callen, Janet Kerwin, Susan Lindsay, Alfons Meindl, Mohan L. Gupta, David Pellman, Elizabeth C. Engle
Argitaratua 2010Artigo -
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Testing the generalizability of ancestry-specific polygenic risk scores to predict prostate cancer in sub-Saharan Africa nork Michelle S. Kim, Daphne Naidoo, Ujani Hazra, Melanie H. Quiver, Wenlong Carl Chen, Corinne Simonti, Paidamoyo Kachambwa, Maxine Harlemon, Ilir Agalliu, Shakuntala Baichoo, P. Fernandez, Ann W. Hsing, Mohamed Jalloh, Sérigne Maguèye Gueye, Lamine Niang, Halimatou Diop‐Ndiaye, Médina Ndoye, Nana Yaa Snyper, Ben Adusei, James E. Mensah, Afua O.D. Abrahams, Richard Biritwum, Andrew A. Adjei, Akindele O. Adebiyi, Olayiwola B. Shittu, Olufemi J. Ogunbiyi, Sikiru Adebayo, Oseremen I. Aisuodionoe-Shadrach, Maxwell M. Nwegbu, Hafees O. Ajibola, Olabode P. Oluwole, Mustapha A. Jamda, Elvira Singh, Audrey Pentz, Maureen Joffe, Burcu F. Darst, David V. Conti, Christopher A. Haiman, Petrus V. Spies, André van der Merwe, Thomas E. Rohan, Judith S. Jacobson, Alfred I. Neugut, Jo McBride, Caroline Andrews, Lindsay N. Petersen, Timothy R. Rebbeck, Joseph Lachance
Argitaratua 2022Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Biology
Gene
Genetics
Medicine
Internal medicine
Mutation
Cancer
Cell biology
Phenotype
Immunology
Neuroscience
Prostate cancer
Anatomy
Biochemistry
Cytokine
Genome-wide association study
Genotype
Immune system
Missense mutation
Oncology
Single-nucleotide polymorphism
Axon
Axon guidance
Cancer research
Demography
Disease
Environmental health
Hypoplasia
Microtubule
Pathology