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Showing results (1201-1210 of 2,049) with videos related to
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Applied and Environmental Microbiology
|
February 11, 1992
Use of colistin-polymyxin B-cellobiose agar for isolation of Vibrio vulnificus from the environment
J D Oliver, K Guthrie, J Preyer, et al.
Nature
|
May 1, 1997
Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese
S Enerbäck, A Jacobsson, E M Simpson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 8, 2005
Pathological aggression in "fierce" mice corrected by human nuclear receptor 2E1
Brett S Abrahams, Melvin C H Kwok, Eric Trinh, et al.
Public Health Nutrition
|
May 2, 2013
Reliability and validity of a short FFQ for assessing the dietary habits of 2-5-year-old children, Sydney, Australia
Victoria M Flood, Li Min Wen, Louise L Hardy, et al.
American Journal of Public Health
|
May 1, 1994
Work-site cholesterol screening and dietary intervention: the Staff Healthy Heart Project. Steering Committee
A Barratt, R Reznik, L Irwig, et al.
Paediatric and Perinatal Epidemiology
|
April 8, 2015
Hospitalisations from 1 to 6 years of age: effects of gestational age and severe neonatal morbidity
Alexandre S Stephens, Samantha J Lain, Christine L Roberts, et al.
Bioinformatics (Oxford, England)
|
June 25, 2008
FIRMA: a method for detection of alternative splicing from exon array data
E Purdom, K M Simpson, M D Robinson, et al.
Patient Education and Counseling
|
March 11, 2009
Development and preliminary evaluation of a bowel cancer screening decision aid for adults with lower literacy
Sian K Smith, Lyndal Trevena, Alexandra Barratt, et al.
Molecular Psychiatry
|
May 24, 2007
Infant serotonin transporter (SLC6A4) promoter genotype is associated with adverse neonatal outcomes after prenatal exposure to serotonin reuptake inhibitor medications
T F Oberlander, R J Bonaguro, S Misri, et al.
BMC Medical Genetics
|
July 28, 2007
Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes
Ravinesh A Kumar, David B Everman, Chad T Morgan, et al.
Page
of 205
Search research articles
Search
Showing results (1201-1210 of 2,049) with videos related to
Sort By:
Page
of 205
Applied and Environmental Microbiology
|
February 11, 1992
Use of colistin-polymyxin B-cellobiose agar for isolation of Vibrio vulnificus from the environment
J D Oliver, K Guthrie, J Preyer, et al.
Nature
|
May 1, 1997
Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese
S Enerbäck, A Jacobsson, E M Simpson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 8, 2005
Pathological aggression in "fierce" mice corrected by human nuclear receptor 2E1
Brett S Abrahams, Melvin C H Kwok, Eric Trinh, et al.
Public Health Nutrition
|
May 2, 2013
Reliability and validity of a short FFQ for assessing the dietary habits of 2-5-year-old children, Sydney, Australia
Victoria M Flood, Li Min Wen, Louise L Hardy, et al.
American Journal of Public Health
|
May 1, 1994
Work-site cholesterol screening and dietary intervention: the Staff Healthy Heart Project. Steering Committee
A Barratt, R Reznik, L Irwig, et al.
Paediatric and Perinatal Epidemiology
|
April 8, 2015
Hospitalisations from 1 to 6 years of age: effects of gestational age and severe neonatal morbidity
Alexandre S Stephens, Samantha J Lain, Christine L Roberts, et al.
Bioinformatics (Oxford, England)
|
June 25, 2008
FIRMA: a method for detection of alternative splicing from exon array data
E Purdom, K M Simpson, M D Robinson, et al.
Patient Education and Counseling
|
March 11, 2009
Development and preliminary evaluation of a bowel cancer screening decision aid for adults with lower literacy
Sian K Smith, Lyndal Trevena, Alexandra Barratt, et al.
Molecular Psychiatry
|
May 24, 2007
Infant serotonin transporter (SLC6A4) promoter genotype is associated with adverse neonatal outcomes after prenatal exposure to serotonin reuptake inhibitor medications
T F Oberlander, R J Bonaguro, S Misri, et al.
BMC Medical Genetics
|
July 28, 2007
Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes
Ravinesh A Kumar, David B Everman, Chad T Morgan, et al.
Page
of 205