Publications by authors named "Susan A Cook"

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Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis.
Muriel T Davisson, Susan A Cook, Ellen C Akeson, Don Liu, Caleb Heffner

Am J Physiol Renal Physiol· June 2015

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Loss of Clcc1 results in ER stress, misfolded protein accumulation, and neurodegeneration.
Yichang Jia, Thomas J Jucius, Susan A Cook, Susan L Ackerman

J Neurosci· February 2015

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A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers.
Ron Korstanje, Christina R Caputo, Rosalinda A Doty, Susan A Cook, Roderick T Bronson

Kidney Int· June 2014

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Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis.
Gayle B Collin, Jungyeon Won, Wanda L Hicks, Susan A Cook, Patsy M Nishina

Invest Ophthalmol Vis Sci· February 2012

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A mouse model for Meckel syndrome type 3.
Susan A Cook, Gayle B Collin, Roderick T Bronson, Jürgen K Naggert, Dong P Liu

J Am Soc Nephrol· April 2009

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Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration.
Jeong Woong Lee, Kirk Beebe, Leslie A Nangle, Jaeseon Jang, Chantal M Longo-Guess, Susan A Cook

Nature· September 2006

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A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Chantal M Longo-Guess, Leona H Gagnon, Susan A Cook, Jian Wu, Qing Y Zheng

Proc Natl Acad Sci U S A· May 2005

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Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.
Kenneth R Johnson, Priscilla W Lane, Susan A Cook, Belinda S Harris, Patricia F Ward-Bailey

Genomics· January 2003

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