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Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo. [electronic resource] by
- 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
Producer: 20071212
In:
The Journal of cell biology vol. 178
Availability: No items available.
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25.
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Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis. [electronic resource] by
- Lopes Floro, Kylie
- Artap, Stanley T
- Preis, Jost I
- Fatkin, Diane
- Chapman, Gavin
- Furtado, Milena B
- Harvey, Richard P
- Hamada, Hiroshi
- Sparrow, Duncan B
- Dunwoodie, Sally L
Producer: 20110620
In:
Human molecular genetics vol. 20
Availability: No items available.
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26.
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Complex SUMO-1 regulation of cardiac transcription factor Nkx2-5. [electronic resource] by
- 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
Producer: 20120228
In:
PloS one vol. 6
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27.
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Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signaling. [electronic resource] by
- Wilkinson, Lorine J
- Neal, Cailda S
- Singh, Reetu R
- Sparrow, Duncan B
- Kurniawan, Nyoman D
- Ju, Adler
- Grieve, Stuart M
- Dunwoodie, Sally L
- Moritz, Karen M
- Little, Melissa H
Producer: 20160222
In:
Kidney international vol. 87
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28.
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Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. [electronic resource] by
- Sparrow, Duncan B
- Faqeih, Eissa Ali
- Sallout, Bahauddin
- Alswaid, Abdulrahman
- Ababneh, Faroug
- Al-Sayed, Moeenaldeen
- Rukban, Hadeel
- Eyaid, Wafaa M
- Kageyama, Ryoichiro
- Ellard, Sian
- Turnpenny, Peter D
- Dunwoodie, Sally L
Producer: 20140326
In:
American journal of medical genetics. Part A vol. 161A
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29.
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Cited1 is required in trophoblasts for placental development and for embryo growth and survival. [electronic resource] by
- 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
Producer: 20040121
In:
Molecular and cellular biology vol. 24
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30.
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SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation. [electronic resource] by
- Blewitt, Marnie E
- Gendrel, Anne-Valerie
- Pang, Zhenyi
- Sparrow, Duncan B
- Whitelaw, Nadia
- Craig, Jeffrey M
- Apedaile, Anwyn
- Hilton, Douglas J
- Dunwoodie, Sally L
- Brockdorff, Neil
- Kay, Graham F
- Whitelaw, Emma
Producer: 20080522
In:
Nature genetics vol. 40
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31.
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Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. [electronic resource] by
- Sparrow, Duncan B
- McInerney-Leo, Aideen
- Gucev, Zoran S
- Gardiner, Brooke
- Marshall, Mhairi
- Leo, Paul J
- Chapman, Deborah L
- Tasic, Velibor
- Shishko, Abduhadi
- Brown, Matthew A
- Duncan, Emma L
- Dunwoodie, Sally L
Producer: 20130903
In:
Human molecular genetics vol. 22
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32.
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Gene-environment interaction demonstrates the vulnerability of the embryonic heart. [electronic resource] by
- O'Reilly, Victoria C
- Lopes Floro, Kylie
- 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
Producer: 20140623
In:
Developmental biology vol. 391
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33.
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Gestational stress induces the unfolded protein response, resulting in heart defects. [electronic resource] by
- Shi, Hongjun
- O'Reilly, Victoria C
- Moreau, Julie L M
- Bewes, Therese R
- Yam, Michelle X
- Chapman, Bogdan E
- Grieve, Stuart M
- Stocker, Roland
- Graham, Robert M
- Chapman, Gavin
- Sparrow, Duncan B
- Dunwoodie, Sally L
Producer: 20170905
In:
Development (Cambridge, England) vol. 143
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34.
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Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects. [electronic resource] by
- McInerney-Leo, Aideen M
- Sparrow, Duncan B
- Harris, Jessica E
- Gardiner, Brooke B
- Marshall, Mhairi S
- O'Reilly, Victoria C
- Shi, Hongjun
- Brown, Matthew A
- Leo, Paul J
- Zankl, Andreas
- Dunwoodie, Sally L
- Duncan, Emma L
Producer: 20151116
In:
Human molecular genetics vol. 24
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35.
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BMP/SMAD1 signaling sets a threshold for the left/right pathway in lateral plate mesoderm and limits availability of SMAD4. [electronic resource] by
- 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
Producer: 20090226
In:
Genes & development vol. 22
Availability: No items available.
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36.
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A mechanism for gene-environment interaction in the etiology of congenital scoliosis. [electronic resource] by
- Sparrow, Duncan B
- Chapman, Gavin
- Smith, Allanceson J
- Mattar, Muhammad Z
- Major, Joelene A
- O'Reilly, Victoria C
- Saga, Yumiko
- Zackai, Elaine H
- Dormans, John P
- Alman, Benjamin A
- McGregor, Lesley
- Kageyama, Ryoichiro
- Kusumi, Kenro
- Dunwoodie, Sally L
Producer: 20120608
In:
Cell vol. 149
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37.
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Gene-environment interaction impacts on heart development and embryo survival. [electronic resource] by
- Moreau, Julie L M
- Kesteven, Scott
- Martin, Ella M M A
- Lau, Kin S
- Yam, Michelle X
- O'Reilly, Victoria C
- Del Monte-Nieto, Gonzalo
- Baldini, Antonio
- Feneley, Michael P
- Moon, Anne M
- Harvey, Richard P
- Sparrow, Duncan B
- Chapman, Gavin
- Dunwoodie, Sally L
Producer: 20200102
In:
Development (Cambridge, England) vol. 146
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38.
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A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. [electronic resource] by
- Szot, Justin O
- Cuny, Hartmut
- Blue, Gillian M
- Humphreys, David T
- Ip, Eddie
- Harrison, Katrina
- Sholler, Gary F
- Giannoulatou, Eleni
- Leo, Paul
- Duncan, Emma L
- Sparrow, Duncan B
- Ho, Joshua W K
- Graham, Robert M
- Pachter, Nicholas
- Chapman, Gavin
- Winlaw, David S
- Dunwoodie, Sally L
Producer: 20190307
In:
Circulation. Genomic and precision medicine vol. 11
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39.
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Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants. [electronic resource] by
- 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
Producer: 20210603
In:
Human molecular genetics vol. 29
Availability: No items available.
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40.
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NAD Deficiency, Congenital Malformations, and Niacin Supplementation. [electronic resource] by
- Shi, Hongjun
- Enriquez, Annabelle
- Rapadas, Melissa
- Martin, Ella M M A
- Wang, Roni
- Moreau, Julie
- Lim, Chai K
- Szot, Justin O
- Ip, Eddie
- Hughes, James N
- Sugimoto, Kotaro
- Humphreys, David T
- McInerney-Leo, Aideen M
- Leo, Paul J
- Maghzal, Ghassan J
- Halliday, Jake
- Smith, Janine
- Colley, Alison
- Mark, Paul R
- Collins, Felicity
- Sillence, David O
- Winlaw, David S
- Ho, Joshua W K
- Guillemin, Gilles J
- Brown, Matthew A
- Kikuchi, Kazu
- Thomas, Paul Q
- Stocker, Roland
- Giannoulatou, Eleni
- Chapman, Gavin
- Duncan, Emma L
- Sparrow, Duncan B
- Dunwoodie, Sally L
Producer: 20170822
In:
The New England journal of medicine vol. 377
Availability: No items available.
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