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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2002 | 1 |
2008 | 1 |
2015 | 1 |
2017 | 2 |
2024 | 0 |
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Page 1
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
N Engl J Med. 2017 Feb 23;376(8):742-754. doi: 10.1056/NEJMoa1609009. Epub 2017 Jan 25.
N Engl J Med. 2017.
PMID: 28121514
Free PMC article.
BCR/ABL P190 transgenic mice develop leukemia in the absence of Crkl.
Hemmeryckx B, Reichert A, Watanabe M, Kaartinen V, de Jong R, Pattengale PK, Groffen J, Heisterkamp N.
Hemmeryckx B, et al.
Oncogene. 2002 May 9;21(20):3225-31. doi: 10.1038/sj.onc.1205452.
Oncogene. 2002.
PMID: 12082638
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Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
Guris DL, Fantes J, Tara D, Druker BJ, Imamoto A.
Guris DL, et al.
Nat Genet. 2001 Mar;27(3):293-8. doi: 10.1038/85855.
Nat Genet. 2001.
PMID: 11242111
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Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation.
Racedo SE, McDonald-McGinn DM, Chung JH, Goldmuntz E, Zackai E, Emanuel BS, Zhou B, Funke B, Morrow BE.
Racedo SE, et al.
Am J Hum Genet. 2015 Feb 5;96(2):235-44. doi: 10.1016/j.ajhg.2014.12.025.
Am J Hum Genet. 2015.
PMID: 25658046
Free PMC article.
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Murine model indicates 22q11.2 signaling adaptor CRKL is a dosage-sensitive regulator of genitourinary development.
Haller M, Mo Q, Imamoto A, Lamb DJ.
Haller M, et al.
Proc Natl Acad Sci U S A. 2017 May 9;114(19):4981-4986. doi: 10.1073/pnas.1619523114. Epub 2017 Apr 24.
Proc Natl Acad Sci U S A. 2017.
PMID: 28439006
Free PMC article.
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Crk and Crk-like play essential overlapping roles downstream of disabled-1 in the Reelin pathway.
Park TJ, Curran T.
Park TJ, et al.
J Neurosci. 2008 Dec 10;28(50):13551-62. doi: 10.1523/JNEUROSCI.4323-08.2008.
J Neurosci. 2008.
PMID: 19074029
Free PMC article.
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