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Comparative Medicine|March 11, 2022
Th1/Th17-mediated Immunity and Protection from Peripheral Neuropathy in Wildtype and IL10<sup>-/-</sup> BALB/c Mice Infected with a Guillain-Barré Syndrome-associated <i>Campylobacter jejuni</i> StrainJean M Brudvig, Matthew M Cluett, Elizabeth U Gensterblum-Miller, et al.
Vaccine|September 6, 2018
Low levels of detectable pertussis antibody among a large cohort of pregnant women in CanadaJames I Brooks, Christopher A Bell, Jenny Rotondo, et al.
Instructional Course Lectures|March 7, 2022
Nonarthroplasty Management of Shoulder Arthritis in the Aging Athlete: Biologics and ArthroscopyJennifer A Bell, Ioanna K Bolia, Brian J Cole, et al.
Ophthalmology|December 17, 1998
Antioxidant nutrient intake and diabetic retinopathy: the San Luis Valley Diabetes StudyE J Mayer-Davis, R A Bell, B A Reboussin, et al.
Microbiology (Reading, England)|December 10, 2003
Variation of the natural transformation frequency of Campylobacter jejuni in liquid shake cultureDavid L Wilson, Julia A Bell, Vincent B Young, et al.
The Journal of Rural Health : Official Journal of the American Rural Health Association and the National Rural Health Care Association|September 18, 2007
Ethnic and sex differences in ownership of preventive health equipment among rural older adults with diabetesRonny A Bell, Thomas A Arcury, Jeanette M Stafford, et al.
Science (New York, N.Y.)|February 5, 1988
Replacements of Pro86 in phage T4 lysozyme extend an alpha-helix but do not alter protein stabilityT Alber, J A Bell, D P Sun, et al.
Journal of the American Medical Directors Association|March 11, 2015
Physical activity and adiposity markers at older ages: accelerometer vs questionnaire dataSéverine Sabia, Pol Cogranne, Vincent T van Hees, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|July 14, 2001
Lower respiratory tract infections in Inuit infants on Baffin IslandA Banerji, A Bell, E L Mills, et al.
Arthritis and Rheumatism|November 16, 2011
Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutationPeter A Bell, Katarzyna A Piróg, Maryline Fresquet, et al.
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