Результаты поиска - Jacqueline K. White
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NH2-terminal sequence of macrophage-expressed natural resistance-associated macrophage protein (Nramp) encodes a proline/serine-rich putative Src homology 3-binding domain. по Chris Barton, Jacqueline K. White, Tamara I. A. Roach, Jenefer M. Blackwell
Опубликовано 1994Artigo -
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Slc11a1, Formerly Nramp1, Is Expressed in Dendritic Cells and Influences Major Histocompatibility Complex Class II Expression and Antigen-Presenting Cell Function по Carmel B. Stober, Sven Brode, Jacqueline K. White, Jean-François Popoff, Jenefer M. Blackwell
Опубликовано 2007Artigo -
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SLC11A1 (formerly NRAMP1) and disease resistance. Microreview по Jenefer M. Blackwell, Tapasree Goswami, Carlton A. Evans, Dean Sibthorpe, Natalie Papo, Jacqueline K. White, Susan Searle, E. Nancy Miller, Christopher S. Peacock, Hiba Mohammed, Muntaser E. Ibrahim
Опубликовано 2001Revisão -
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High-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice по Christine Podrini, Emma L. Cambridge, Christopher J. Lelliott, Damian M. Carragher, Jeanne Estabel, Anna-Karin Gerdin, Natasha A. Karp, Cheryl L. Scudamore, Ramiro Ramírez‐Solis, Jacqueline K. White
Опубликовано 2013Artigo -
6
Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen по Kifayathullah Liakath‐Ali, Valerie E. Vancollie, Emma Heath, Damian Smedley, Jeanne Estabel, David Sunter, Tia DiTommaso, Jacqueline K. White, Ramiro Ramírez‐Solis, Ian Smyth, Karen P. Steel, Fiona M. Watt
Опубликовано 2014Artigo -
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SLC11A1 (formerly NRAMP1) and susceptibility to visceral leishmaniasis in The Sudan по Hiba S. Mohamed, Muntaser E. Ibrahim, E. Nancy Miller, Jacqueline K. White, Heather J. Cordell, Joanna M. M. Howson, Christopher S. Peacock, Eltahir Awad Gasim Khalil, A.M. El Hassan, Jenefer M. Blackwell
Опубликовано 2003Artigo -
8
Mcph1-Deficient Mice Reveal a Role for MCPH1 in Otitis Media по Jing Chen, Neil J. Ingham, Simon Clare, Claire Raisen, Valerie E. Vancollie, Ozama Ismail, Rebecca E. McIntyre, Stephen H. Tsang, Vinit B. Mahajan, Gordon Dougan, David J. Adams, Jacqueline K. White, Karen P. Steel
Опубликовано 2013Artigo -
9
Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss по Jing Chen, Neil J. Ingham, John J. Kelly, Shalini Jadeja, David Goulding, Johanna Pass, Vinit B. Mahajan, Stephen H. Tsang, Anastasia Nijnik, Ian J. Jackson, Jacqueline K. White, Andrew Forge, Daniel J. Jagger, Karen P. Steel
Опубликовано 2014Artigo -
10
Rapid-Throughput Skeletal Phenotyping of 100 Knockout Mice Identifies 9 New Genes That Determine Bone Strength по J. H. Duncan Bassett, Apostolos Gogakos, Jacqueline K. White, Holly Evans, Richard Jacques, Anne H. van der Spek, Ramiro Ramírez‐Solis, Edward J. Ryder, David Sunter, A. Boyde, Michael J. Campbell, Peter I. Croucher, Graham R. Williams
Опубликовано 2012Artigo -
11
Generation and Characterization of a Knockout Mouse of an Enhancer of<i>EBF3</i> по Emily Cordova Hurtado, Janine M. Wotton, Alexander O. D. Gulka, Crystal Burke, Jeffrey K. Ng, Ibrahim Bah, Juana G. Manuel, Hillary B. Heins, Stephen A. Murray, David U. Gorkin, Jacqueline K. White, Kevin A. Peterson, Tychele N. Turner
Опубликовано 2025Pré-impressão -
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Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing по Annalisa Buniello, Neil J. Ingham, Morag A. Lewis, Andreea C Huma, Raquel Martínez‐Vega, Isabel Varela‐Nieto, Gema Vizcay‐Barrena, Roland A. Fleck, Oliver Houston, Tanaya Bardhan, Stuart L. Johnson, Jacqueline K. White, Huijun Yuan, Walter Marcotti, Karen P. Steel
Опубликовано 2016Artigo -
13
Mouse screen reveals multiple new genes underlying mouse and human hearing loss по Neil J. Ingham, Selina Pearson, Valerie E. Vancollie, Victoria Rook, Morag A. Lewis, Jing Chen, Annalisa Buniello, Elisa Martelletti, Lorenzo Preite, Chi Chung Lam, Felix D. Weiss, Zöe Powis, Pim Suwannarat, Christopher J. Lelliott, Sally J. Dawson, Jacqueline K. White, Karen P. Steel
Опубликовано 2019Artigo -
14
Into the Wild: A novel wild-derived inbred strain resource expands the genomic and phenotypic diversity of laboratory mouse models по Beth L. Dumont, Daniel M. Gatti, Mallory A. Ballinger, Dana Lin, Megan Phifer‐Rixey, Michael J. Sheehan, Taichi A. Suzuki, Lydia K. Wooldridge, Hilda Opoku Frempong, Raman Akinyanju Lawal, Gary A. Churchill, Cathleen Lutz, Nadia Rosenthal, Jacqueline K. White, Michael W. Nachman
Опубликовано 2024Artigo -
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Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis по Leslie O. Goodwin, Erik Splinter, Tiffany L. Davis, Rachel Urban, Hao He, Robert E. Braun, Elissa J. Chesler, Vivek Kumar, Max van Min, Juliet Ndukum, Vivek M. Philip, Laura G. Reinholdt, Karen L. Svenson, Jacqueline K. White, Michael Sasner, Cathleen Lutz, Stephen A. Murray
Опубликовано 2019Artigo -
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Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity по Kevin A. Peterson, Sam Khalouei, Nour Hanafi, Joshua A. Wood, Denise G. Lanza, Lauri G. Lintott, Brandon Willis, John R. Seavitt, Robert E. Braun, Mary E. Dickinson, Jacqueline K. White, K. C. Kent Lloyd, Jason D. Heaney, Stephen A. Murray, Arun Ramani, Lauryl M. J. Nutter
Опубликовано 2023Artigo -
17
Placentation defects are highly prevalent in embryonic lethal mouse mutants по Vicente Pérez-García, Elena Fineberg, Robert Wilson, Alexander Murray, Cecilia Mazzeo, Catherine Tudor, Arnold R. Sienerth, Jacqueline K. White, Elizabeth Tuck, Edward J. Ryder, Diane Gleeson, Emma Siragher, Hannah Wardle‐Jones, Nicole Staudt, Neha Wali, John Collins, Stefan H. Geyer, Elisabeth M. Busch‐Nentwich, Antonella Galli, James C. Smith, Elizabeth J. Robertson, David J. Adams, Wolfgang J. Weninger, Timothy J. Mohun, Myriam Hemberger
Опубликовано 2018Artigo -
18
Disruption of Mouse Cenpj, a Regulator of Centriole Biogenesis, Phenocopies Seckel Syndrome по Rebecca E. McIntyre, Pavithra L. Chavali, Ozama Ismail, Damian M. Carragher, Gabriela Sánchez-Andrade, Josep V. Forment, Beiyuan Fu, Martin Del Castillo Velasco‐Herrera, Andrew Edwards, Louise van der Weyden, Fengtang Yang, Ramiro Ramírez‐Solis, Jeanne Estabel, Ferdia A. Gallagher, Darren W. Logan, Mark J. Arends, Stephen H. Tsang, Vinit B. Mahajan, Cheryl L. Scudamore, Jacqueline K. White, Stephen P. Jackson, Fanni Gergely, David J. Adams
Опубликовано 2012Artigo -
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Accelerating functional gene discovery in osteoarthritis по Natalie C. Butterfield, Katherine F. Curry, Julia Steinberg, Hannah F. Dewhurst, Davide Komla‐Ebri, Naila S. Mannan, Anne‐Tounsia Adoum, Victoria D. Leitch, John G. Logan, Julian Waung, Elena J. Ghirardello, Lorraine Southam, Scott E. Youlten, J. Mark Wilkinson, Elizabeth A. McAninch, Valerie E. Vancollie, Fiona Kussy, Jacqueline K. White, Christopher J. Lelliott, David J. Adams, Richard Jacques, Antônio C. Bianco, A. Boyde, Eleftheria Zeggini, Peter I. Croucher, Graham R. Williams, J. H. Duncan Bassett
Опубликовано 2021Artigo -
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Deficiency for the Ubiquitin Ligase UBE3B in a Blepharophimosis-Ptosis-Intellectual-Disability Syndrome по Lina Basel‐Vanagaite, Bruno Dallapiccola, Ramiro Ramírez‐Solis, Alexandra Segref, Hölger Thiele, Andrew Edwards, Mark J. Arends, Xavier Miró, Jacqueline K. White, Julie Désir, Marc Abramowicz, Maria Lisa Dentici, Francesca Romana Lepri, Kay Hofmann, Adi Har‐Zahav, Edward J. Ryder, Natasha A. Karp, Jeanne Estabel, Anna-Karin Gerdin, Christine Podrini, Neil J. Ingham, Janine Altmüller, Gudrun Nürnberg, Peter Frommolt, Sonia Abdelhak, Metsada Pasmanik‐Chor, Osnat Konen, Richard I. Kelley, Mordechai Shohat, Peter Nürnberg, Jonathan Flint, Karen P. Steel, Thorsten Hoppe, Christian Kubisch, David J. Adams, Guntram Borck
Опубликовано 2012Artigo
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Biology
Gene
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Phenotype
Computational biology
Medicine
Cell biology
Genome
Gene knockout
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Knockout mouse
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Single-nucleotide polymorphism
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