Search research articles
Contact Us
Filters
Showing results (41-50 of 63) with videos related to
Page
of 7
Sort By:
Pediatric Research
|
October 20, 2001
Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards
A Hamvas, M Trusgnich, H Brice, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
February 26, 2015
Respiratory failure in a term infant with cis and trans mutations in ABCA3
T Jackson, D J Wegner, F V White, et al.
The New England Journal of Medicine
|
March 26, 1992
Molecular heterogeneity of C2 deficiency
C A Johnson, P Densen, R A Wetsel, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
November 1, 1982
Biosynthesis of a structurally abnormal C2 complement protein by macrophages from C2-deficient guinea pigs
G Goldberger, F S Cole, L P Einstein, et al.
Lancet (London, England)
|
July 15, 1978
Effect of phototherapy on sister chromatid exchange in premature infants
A L Schwartz, F S Cole, F Fiedorek, et al.
The Journal of Clinical Investigation
|
April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphatase
M P Whyte, J D Mahuren, K N Fedde, et al.
Clinical Immunology and Immunopathology
|
May 1, 1983
Complement biosynthesis by human bronchoalveolar macrophages
F S Cole, W J Matthews, T H Rossing, et al.
Gastroenterology
|
August 1, 1983
Isolation and characterization of resident macrophages from guinea pig and human intestine
H S Winter, F S Cole, L M Huffer, et al.
Pediatric Research
|
June 12, 2010
Surfactant protein-C promoter variants associated with neonatal respiratory distress syndrome reduce transcription
Jennifer A Wambach, Ping Yang, Daniel J Wegner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1985
The cellular defect in alpha 1-proteinase inhibitor (alpha 1-PI) deficiency is expressed in human monocytes and in Xenopus oocytes injected with human liver mRNA
D H Perlmutter, R M Kay, F S Cole, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 63) with videos related to
Sort By:
Page
of 7
Pediatric Research
|
October 20, 2001
Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards
A Hamvas, M Trusgnich, H Brice, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
February 26, 2015
Respiratory failure in a term infant with cis and trans mutations in ABCA3
T Jackson, D J Wegner, F V White, et al.
The New England Journal of Medicine
|
March 26, 1992
Molecular heterogeneity of C2 deficiency
C A Johnson, P Densen, R A Wetsel, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
November 1, 1982
Biosynthesis of a structurally abnormal C2 complement protein by macrophages from C2-deficient guinea pigs
G Goldberger, F S Cole, L P Einstein, et al.
Lancet (London, England)
|
July 15, 1978
Effect of phototherapy on sister chromatid exchange in premature infants
A L Schwartz, F S Cole, F Fiedorek, et al.
The Journal of Clinical Investigation
|
April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphatase
M P Whyte, J D Mahuren, K N Fedde, et al.
Clinical Immunology and Immunopathology
|
May 1, 1983
Complement biosynthesis by human bronchoalveolar macrophages
F S Cole, W J Matthews, T H Rossing, et al.
Gastroenterology
|
August 1, 1983
Isolation and characterization of resident macrophages from guinea pig and human intestine
H S Winter, F S Cole, L M Huffer, et al.
Pediatric Research
|
June 12, 2010
Surfactant protein-C promoter variants associated with neonatal respiratory distress syndrome reduce transcription
Jennifer A Wambach, Ping Yang, Daniel J Wegner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1985
The cellular defect in alpha 1-proteinase inhibitor (alpha 1-PI) deficiency is expressed in human monocytes and in Xenopus oocytes injected with human liver mRNA
D H Perlmutter, R M Kay, F S Cole, et al.
Page
of 7