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Blood Cells, Molecules & Diseases
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June 6, 1998
Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patients
H Ida, O M Rennert, T Ito, et al.
Archives of Biochemistry and Biophysics
|
November 1, 1979
A polyamine-conjugated peptide isolated from human plasma
T W Seale, W Y Chan, J Shulka, et al.
Clinical Pediatrics
|
June 1, 1972
The detection of the heterozygote and homozygote in cystic fibrosis by short term lymphocyte culture studies: a defect in RNA methylation
O M Rennert, J L Frias, R L Julius, et al.
Clinical Dysmorphology
|
August 24, 1999
Case report on SHORT syndrome
S H Joo, M Raygada, S Gibney, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 1, 1979
Polyamine conjugates and total polyamine concentrations in human amniotic fluid
W Y Chan, T W Seale, J B Shukla, et al.
Birth Defects Original Article Series
|
January 1, 1982
A case of mosaic Down syndrome with 46,XY/47,XY, + 21/46,XY, + fragment cell lines
R S Muneer, P J Stupca, W H Simon, et al.
Metabolism: Clinical and Experimental
|
December 1, 1985
Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet
D L Donaldson, D M Lee, C C Smith, et al.
Epigenetics
|
November 4, 2011
Expression of human NAA11 (ARD1B) gene is tissue-specific and is regulated by DNA methylation
Alan L Y Pang, Jessica Clark, Wai-Yee Chan, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 7, 2011
Methylation profiling using methylated DNA immunoprecipitation and tiling array hybridization
Hoi-Hung Cheung, Tin-Lap Lee, Owen M Rennert, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 9, 1980
Polyamine metabolism in Menkes kinky hair disease
O M Rennert, W Y Chan, H Hidalgo, et al.
Page
of 25
Search research articles
Search
Showing results (141-150 of 250) with videos related to
Sort By:
Page
of 25
Blood Cells, Molecules & Diseases
|
June 6, 1998
Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patients
H Ida, O M Rennert, T Ito, et al.
Archives of Biochemistry and Biophysics
|
November 1, 1979
A polyamine-conjugated peptide isolated from human plasma
T W Seale, W Y Chan, J Shulka, et al.
Clinical Pediatrics
|
June 1, 1972
The detection of the heterozygote and homozygote in cystic fibrosis by short term lymphocyte culture studies: a defect in RNA methylation
O M Rennert, J L Frias, R L Julius, et al.
Clinical Dysmorphology
|
August 24, 1999
Case report on SHORT syndrome
S H Joo, M Raygada, S Gibney, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 1, 1979
Polyamine conjugates and total polyamine concentrations in human amniotic fluid
W Y Chan, T W Seale, J B Shukla, et al.
Birth Defects Original Article Series
|
January 1, 1982
A case of mosaic Down syndrome with 46,XY/47,XY, + 21/46,XY, + fragment cell lines
R S Muneer, P J Stupca, W H Simon, et al.
Metabolism: Clinical and Experimental
|
December 1, 1985
Glucose tolerance and plasma lipid distributions in rats fed a high-sucrose, high-cholesterol, low-chromium diet
D L Donaldson, D M Lee, C C Smith, et al.
Epigenetics
|
November 4, 2011
Expression of human NAA11 (ARD1B) gene is tissue-specific and is regulated by DNA methylation
Alan L Y Pang, Jessica Clark, Wai-Yee Chan, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
December 7, 2011
Methylation profiling using methylated DNA immunoprecipitation and tiling array hybridization
Hoi-Hung Cheung, Tin-Lap Lee, Owen M Rennert, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 9, 1980
Polyamine metabolism in Menkes kinky hair disease
O M Rennert, W Y Chan, H Hidalgo, et al.
Page
of 25