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American Journal of Human Genetics
|
June 10, 2008
Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instability
Søren W Gersting, Kristina F Kemter, Michael Staudigl, et al.
Biochimica Et Biophysica Acta
|
December 14, 2005
Role of Pex19p in the targeting of PMP70 to peroxisome
Yoshinori Kashiwayama, Kota Asahina, Hiroyuki Shibata, et al.
Nature Medicine
|
December 7, 2007
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease
Dominik Hartl, Philipp Latzin, Peter Hordijk, et al.
American Journal of Human Genetics
|
November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency
Andreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Journal of Lipid Research
|
February 21, 2012
In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranes
Regina Ensenauer, Ralph Fingerhut, Sonja C Schriever, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
February 26, 2017
Modification of the fatty acid composition of an obesogenic diet improves the maternal and placental metabolic environment in obese pregnant mice
Martina Gimpfl, Jan Rozman, Maik Dahlhoff, et al.
Human Molecular Genetics
|
February 25, 2010
Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo
Søren W Gersting, Florian B Lagler, Anna Eichinger, et al.
Plos Medicine
|
October 30, 2018
Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort study
Delphina Gomes, Rüdiger von Kries, Maria Delius, et al.
Human Mutation
|
July 13, 2006
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment
Sonja C Stadler, Roman Polanetz, Esther M Maier, et al.
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of 4
Search research articles
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Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
American Journal of Human Genetics
|
June 10, 2008
Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instability
Søren W Gersting, Kristina F Kemter, Michael Staudigl, et al.
Biochimica Et Biophysica Acta
|
December 14, 2005
Role of Pex19p in the targeting of PMP70 to peroxisome
Yoshinori Kashiwayama, Kota Asahina, Hiroyuki Shibata, et al.
Nature Medicine
|
December 7, 2007
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease
Dominik Hartl, Philipp Latzin, Peter Hordijk, et al.
American Journal of Human Genetics
|
November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency
Andreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Journal of Lipid Research
|
February 21, 2012
In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranes
Regina Ensenauer, Ralph Fingerhut, Sonja C Schriever, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
February 26, 2017
Modification of the fatty acid composition of an obesogenic diet improves the maternal and placental metabolic environment in obese pregnant mice
Martina Gimpfl, Jan Rozman, Maik Dahlhoff, et al.
Human Molecular Genetics
|
February 25, 2010
Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo
Søren W Gersting, Florian B Lagler, Anna Eichinger, et al.
Plos Medicine
|
October 30, 2018
Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort study
Delphina Gomes, Rüdiger von Kries, Maria Delius, et al.
Human Mutation
|
July 13, 2006
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment
Sonja C Stadler, Roman Polanetz, Esther M Maier, et al.
Page
of 4