Christina L. McHenry

University of Michigan–Ann Arbor — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

13h-index1.8kcitations29works0.02yr avg
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Research Topics

Retinal Development and Disorders(18), Asthma and respiratory diseases(6), Retinal Diseases and Treatments(6), Respiratory viral infections research(5), Retinoids in leukemia and cellular processes(5)

Publications29 total

Macrophage/epithelial cell CCL2 contributes to rhinovirus-induced hyperresponsiveness and inflammation in a mouse model of allergic airways disease
American Journal of Physiology-Lung Cellular and Molecular Physiology·2012· 62 cited
Nasal cytokine responses to natural colds in asthmatic children
Clinical & Experimental Allergy·2012· 49 citedOpen Access
Rhinovirus Infection of Allergen-Sensitized and -Challenged Mice Induces Eotaxin Release from Functionally Polarized Macrophages
The Journal of Immunology·2010· 113 citedOpen Access
Effects Of Early Life Rhinovirus Infection On Lung Inflammation
2010
Pilot Study To Characterize Cytokine Responses In Viral Exacerbations Of Childhood Asthma
2010
CC Chemokines And RV-Induced Asthma Exacerbations
2010
DHRS3 (retSDR1) from the Family of Short-Chain Dehydrogenases/Reductases: Analysis of Enzyme Activity, Expression, and Sequence Variants
2010
Role of Double-Stranded RNA Pattern Recognition Receptors in Rhinovirus-Induced Airway Epithelial Cell Responses
The Journal of Immunology·2009· 243 citedOpen Access
Differential Regulation of Rhinovirus-Induced Airway Epithelial Responses by ERK and JNK.
2009
Human Rhinovirus 1B Exposure Induces Phosphatidylinositol 3-Kinase–dependent Airway Inflammation in Mice
American Journal of Respiratory and Critical Care Medicine·2008· 127 citedOpen Access
Visual Cycle Function Is Not Limited by Rdh12-Deficiency in Knockout Mice
2007
Targeted Disruption of the Murine Retinal Dehydrogenase Gene <i>Rdh12</i> Does Not Limit Visual Cycle Function
Molecular and Cellular Biology·2006· 67 citedOpen Access
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle
Human Molecular Genetics·2006· 2 cited
Retinal degeneration associated with RDH12 mutations results from decreased 11- cis retinal synthesis due to disruption of the visual cycle
Human Molecular Genetics·2005· 108 citedOpen Access
RDH12: A New Member of the Family of Visual Cycle Disease Genes
2005
Erratum: Corrigendum: Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause severe childhood-onset retinal dystrophy
Nature Genetics·2004· 3 citedOpen Access
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy
Nature Genetics·2004· 244 cited
MERTK Arginine-844-Cysteine in a Patient with Severe Rod-Cone Dystrophy: Loss of Mutant Protein Function in Transfected Cells
Investigative Ophthalmology & Visual Science·2004· 82 cited
MERTK R844C Mutant Shows Reduced Phosphorylation Activity in Transfected Cells and is Associated with Severe Rod-Cone Dystrophy
2003
Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively
The American Journal of Human Genetics·2002· 151 citedOpen Access
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Frequent Co-authors

Debra A. Thompson(10), Paul A. Sieving(10), Andreas Gal(9), Marc B. Hershenson(8), Christian A. Hübner(7), Deepti R. Nagarkar(6), Kecia L. Feathers(6), Samuel G. Jacobson(5), Andreas Janecke(5), Gerd Utermann(5), Emily Bowman(5), Dina Schneider(5), Bernd Wissinger(4), J. Kelley Bentley(4), Toby C. Lewis(4), Ricardo Fujita(4), Anand Swaroop(4), Eberhart Zrenner(3), John R. Heckenlively(3), Qiong Wang(3)