Kết quả tìm kiếm - Gavin Chapman
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High levels of Notch signaling down-regulate Numb and Numblike Bằng Gavin Chapman, Lining Liu, Cecilia Sahlgren, Camilla Dahlqvist, Urban Lendahl
Được phát hành 2006Artigo -
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Notch4 reveals a novel mechanism regulating Notch signal transduction Bằng Alexander C. James, Justin O. Szot, Kala Iyer, Joelene Major, Sharon E. Pursglove, Gavin Chapman, Sally L. Dunwoodie
Được phát hành 2014Artigo -
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Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease Bằng Morgan Newman, Lachlan Wilson, Giuseppe Verdile, Anne Lim, Imran Khan, Seyyed Hani Moussavi Nik, Sharon E. Pursglove, Gavin Chapman, Ralph N. Martins, Michael Lardelli
Được phát hành 2013Artigo -
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Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo Bằng Insa Geffers, Katrin Serth, Gavin Chapman, Robert Jaekel, Karin Schuster-Gossler, Ralf Cordes, Duncan B. Sparrow, Elisabeth Kremmer, Sally L. Dunwoodie, Thomas Klein, Achim Gossler
Được phát hành 2007Artigo -
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Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype Bằng Duncan B. Sparrow, Gavin Chapman, Merridee A. Wouters, Neil V. Whittock, Sian Ellard, Diane Fatkin, Peter D. Turnpenny, Kenro Kusumi, Daniel J. Sillence, Sally L. Dunwoodie
Được phát hành 2005Artigo -
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Loss of Cited2 causes congenital heart disease by perturbing left–right patterning of the body axis Bằng Kylie Lopes Floro, Stanley T Artap, Jost I. Preis, Diane Fatkin, Gavin Chapman, Milena B. Furtado, Richard P. Harvey, Hiroshi Hamada, Duncan B. Sparrow, Sally L. Dunwoodie
Được phát hành 2010Artigo -
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Gestational stress induces the unfolded protein response, resulting in heart defects Bằng Hongjun Shi, Victoria C. O׳Reilly, Julie Moreau, Therese R. Bewes, Michelle Yam, Bogdan E. Chapman, Stuart M. Grieve, Roland Stocker, Robert M. Graham, Gavin Chapman, Duncan B. Sparrow, Sally L. Dunwoodie
Được phát hành 2016Artigo -
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A Mechanism for Gene-Environment Interaction in the Etiology of Congenital Scoliosis Bằng Duncan B. Sparrow, Gavin Chapman, Allanceson Smith, Muhammad Z. Mattar, Joelene Major, Victoria C. O׳Reilly, Yumiko Saga, Elaine H. Zackai, John P. Dormans, Benjamin A. Alman, Lesley McGregor, Ryoichiro Kageyama, Kenro Kusumi, Sally L. Dunwoodie
Được phát hành 2012Artigo -
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Gene-environment interaction impacts on heart development and embryo survival Bằng Julie Moreau, Scott Kesteven, Ella MMA Martin, Kin S. Lau, Michelle Yam, Victoria C. O׳Reilly, Gonzalo del Monte‐Nieto, Antonio Baldini, Michael P. Feneley, Anne Moon, Richard P. Harvey, Duncan B. Sparrow, Gavin Chapman, Sally L. Dunwoodie
Được phát hành 2019Artigo -
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Novel role for endogenous mitochondrial formylated peptide-driven formyl peptide receptor 1 signalling in acute respiratory distress syndrome Bằng David A. Dorward, Christopher D. Lucas, Mary K. Doherty, Gavin Chapman, Emma Scholefield, Andrew Conway Morris, Jennifer M. Felton, Tiina Kipari, Duncan C. Humphries, Calum T. Robb, A. John Simpson, Phillip D. Whitfield, Christopher Haslett, Kevin Dhaliwal, Adriano G. Rossi
Được phát hành 2017Artigo -
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Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders Bằng Justin O. Szot, Carla Campagnolo, Ye Cao, Kavitha R. Iyer, Hartmut Cuny, Thomas A. Drysdale, Josue Flores-Daboub, Weimin Bi, Lauren Westerfield, Pengfei Liu, Tse Ngong Leung, Kwong Wai Choy, Gavin Chapman, Rui Xiao, Victoria Mok Siu, Sally L. Dunwoodie
Được phát hành 2019Artigo -
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NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets Bằng Romaric Bouveret, Ashley J. Waardenberg, Nicole Schönrock, Mirana Ramialison, Tram B. Doan, Daniëlle de Jong, Antoine Bondue, Gurpreet Kaur, Stephanie Mohamed, Hananeh Fonoudi, C.M. Chen, Merridee A. Wouters, Shoumo Bhattacharya, Nicolas Plachta, Sally L. Dunwoodie, Gavin Chapman, Cédric Blanpain, Richard P. Harvey
Được phát hành 2015Artigo -
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A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data Bằng Justin O. Szot, Hartmut Cuny, Gillian M. Blue, David T. Humphreys, Eddie Ip, Katrina Harrison, Gary F. Sholler, Eleni Giannoulatou, Paul Leo, Emma L. Duncan, Duncan B. Sparrow, Joshua W. K. Ho, Robert M. Graham, Nicholas Pachter, Gavin Chapman, David S. Winlaw, Sally L. Dunwoodie
Được phát hành 2018Artigo -
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Identification of clinically actionable variants from genome sequencing of families with congenital heart disease Bằng Dimuthu Alankarage, Eddie Ip, Justin O. Szot, Jacob E. Munro, Gillian M. Blue, Katrina Harrison, Hartmut Cuny, Annabelle Enriquez, Michael Troup, David T. Humphreys, Meredith Wilson, Richard P. Harvey, Gary F. Sholler, Robert M. Graham, Joshua W. K. Ho, Edwin P. Kirk, Nicholas Pachter, Gavin Chapman, David S. Winlaw, Eleni Giannoulatou, Sally L. Dunwoodie
Được phát hành 2018Artigo -
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Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants Bằng Gavin Chapman, Julie Moreau, I P Eddie, Justin O. Szot, Kavitha R. Iyer, Hongjun Shi, Michelle Yam, Victoria C. O׳Reilly, Annabelle Enriquez, Joelene A Greasby, Dimuthu Alankarage, Ella MMA Martin, Bernadette Hanna, Matthew Edwards, Steven Monger, Gillian M. Blue, David S. Winlaw, Helen E. Ritchie, Stuart M. Grieve, Eleni Giannoulatou, Duncan B. Sparrow, Sally L. Dunwoodie
Được phát hành 2019Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
Cell biology
Phenotype
Medicine
Embryonic stem cell
Signal transduction
Internal medicine
Notch signaling pathway
Biochemistry
Disease
Mesoderm
Bioinformatics
Embryo
Mutation
Chemistry
Embryogenesis
Heart disease
Mutant
Notch proteins
Receptor
Anatomy
Enzyme
Epistemology
Heart development
Hypoxia (environmental)
Mechanism (biology)
Missense mutation
NAD+ kinase