A simplified method of generating transgenic Xenopus

由 Sparrow, Duncan B., Latinkic, Branko, Mohun, Tim J.
出版 2000

Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis

由 Sparrow, Duncan B, Sillence, David, Wouters, Merridee A, Turnpenny, Peter D, Dunwoodie, Sally L
出版 2010

Evolution of distinct EGF domains with specific functions

由 Wouters, Merridee A., Rigoutsos, Isidore, Chu, Carmen K., Feng, Lina L., Sparrow, Duncan B., Dunwoodie, Sally L.
出版 2005

Mutated MESP2 Causes Spondylocostal Dysostosis in Humans

由 Whittock, Neil V., Sparrow, Duncan B., Wouters, Merridee A., Sillence, David, Ellard, Sian, Dunwoodie, Sally L., Turnpenny, Peter D.
出版 2004

Cyclical expression of the Notch/Wnt regulator Nrarp requires modulation by Dll3 in somitogenesis

由 Sewell, William, Sparrow, Duncan B., Smith, Allanceson J., Gonzalez, Dorian M., Rappaport, Eric F., Dunwoodie, Sally L., Kusumi, Kenro
出版 2009

Placental Insufficiency Associated with Loss of Cited1 Causes Renal Medullary Dysplasia

由 Sparrow, Duncan B., Boyle, Scott C., Sams, Rebecca S., Mazuruk, Bogdan, Zhang, Li, Moeckel, Gilbert W., Dunwoodie, Sally L., de Caestecker, Mark P.
出版 2009

Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo

由 Geffers, Insa, Serth, Katrin, Chapman, Gavin, Jaekel, Robert, Schuster-Gossler, Karin, Cordes, Ralf, Sparrow, Duncan B., Kremmer, Elisabeth, Dunwoodie, Sally L., Klein, Thomas, Gossler, Achim
出版 2007

Complex SUMO-1 Regulation of Cardiac Transcription Factor Nkx2-5

由 Costa, Mauro W., Lee, Stella, Furtado, Milena B., Xin, Li, Sparrow, Duncan B., Martinez, Camila G., Dunwoodie, Sally L., Kurtenbach, Eleonora, Mohun, Tim, Rosenthal, Nadia, Harvey, Richard P.
出版 2011

Cited1 Is Required in Trophoblasts for Placental Development and for Embryo Growth and Survival

由 Rodriguez, Tristan A., Sparrow, Duncan B., Scott, Annabelle N., Withington, Sarah L., Preis, Jost I., Michalicek, Jan, Clements, Melanie, Tsang, Tania E., Shioda, Toshi, Beddington, Rosa S. P., Dunwoodie, Sally L.
出版 2004

The Small Muscle-Specific Protein Csl Modifies Cell Shape and Promotes Myocyte Fusion in an Insulin-like Growth Factor 1–Dependent Manner

由 Palmer, Steve, Groves, Nicola, Schindeler, Aaron, Yeoh, Thomas, Biben, Christine, Wang, Cheng-Chun, Sparrow, Duncan B., Barnett, Louise, Jenkins, Nancy A., Copeland, Neal G., Koentgen, Frank, Mohun, Tim, Harvey, Richard P.
出版 2001

Gene–environment interaction demonstrates the vulnerability of the embryonic heart

由 O'Reilly, Victoria C., Floro, Kylie Lopes, Shi, Hongjun, Chapman, Bogdan E., Preis, Jost I., James, Alexander C., Chapman, Gavin, Harvey, Richard P., Johnson, Randall S., Grieve, Stuart M., Sparrow, Duncan B., Dunwoodie, Sally L.
發表在 Dev Biol (2014)

BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4

由 Furtado, Milena B., Solloway, Mark J., Jones, Vanessa J., Costa, Mauro W., Biben, Christine, Wolstein, Orit, Preis, Jost I., Sparrow, Duncan B., Saga, Yumiko, Dunwoodie, Sally L., Robertson, Elizabeth J., Tam, Patrick P.L., Harvey, Richard P.
出版 2008

Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant

由 Jiang, He, Hooper, Charlotte, Kelly, Matthew, Steeples, Violetta, Simon, Jillian N., Beglov, Julia, Azad, Amar J., Leinhos, Lisa, Bennett, Pauline, Ehler, Elisabeth, Kalisch-Smith, Jacinta I., Sparrow, Duncan B., Fischer, Roman, Heilig, Raphael, Isackson, Henrik, Ehsan, Mehroz, Patone, Giannino, Huebner, Norbert, Davies, Benjamin, Watkins, Hugh, Gehmlich, Katja
發表在 Basic Res Cardiol (2021)

Maternal iron deficiency perturbs embryonic cardiovascular development in mice

由 Kalisch-Smith, Jacinta I., Ved, Nikita, Szumska, Dorota, Munro, Jacob, Troup, Michael, Harris, Shelley E., Rodriguez-Caro, Helena, Jacquemot, Aimée, Miller, Jack J., Stuart, Eleanor M., Wolna, Magda, Hardman, Emily, Prin, Fabrice, Lana-Elola, Eva, Aoidi, Rifdat, Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Mohun, Timothy J., Lakhal-Littleton, Samira, De Val, Sarah, Giannoulatou, Eleni, Sparrow, Duncan B.
發表在 Nat Commun (2021)

Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants

由 Chapman, Gavin, Moreau, Julie L M, I P, Eddie, Szot, Justin O, Iyer, Kavitha R, Shi, Hongjun, Yam, Michelle X, O’Reilly, Victoria C, Enriquez, Annabelle, Greasby, Joelene A, Alankarage, Dimuthu, Martin, Ella M M A, Hanna, Bernadette C, Edwards, Matthew, Monger, Steven, Blue, Gillian M, Winlaw, David S, Ritchie, Helen E, Grieve, Stuart M, Giannoulatou, Eleni, Sparrow, Duncan B, Dunwoodie, Sally L
發表在 Hum Mol Genet (2020)

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

由 Martin, Ella M M A, Enriquez, Annabelle, Sparrow, Duncan B, Humphreys, David T, McInerney-Leo, Aideen M, Leo, Paul J, Duncan, Emma L, Iyer, Kavitha R, Greasby, Joelene A, Ip, Eddie, Giannoulatou, Eleni, Sheng, Delicia, Wohler, Elizabeth, Dimartino, Clémantine, Amiel, Jeanne, Capri, Yline, Lehalle, Daphné, Mory, Adi, Wilnai, Yael, Lebenthal, Yael, Gharavi, Ali G, Krzemień, Grażyna G, Miklaszewska, Monika, Steiner, Robert D, Raggio, Cathy, Blank, Robert, Baris Feldman, Hagit, Milo Rasouly, Hila, Sobreira, Nara L M, Jobling, Rebekah, Gordon, Christopher T, Giampietro, Philip F, Dunwoodie, Sally L, Chapman, Gavin
發表在 Hum Mol Genet (2020)