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Molecular Genetics and Metabolism
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May 21, 2024
A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduria
Yu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
The Journal of Physical Chemistry. A
|
August 5, 2017
Chiral Thiophene Sulfonamide-A Challenge for VOA Calculations
Joanna E Rode, Jan Cz Dobrowolski, Krzysztof Lyczko, et al.
Biorxiv : the Preprint Server for Biology
|
February 13, 2023
A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatment
Yu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
September 12, 2025
Concentrations of adrenocorticotropic hormone too low to effect cortisol enhance osteogenesis in vitro and in vivo
Irina L Tourkova, Reed A Rankin, Quitterie C Larrouture, et al.
International Journal of Molecular Sciences
|
May 27, 2023
Prenatal Fumonisin Exposure Impairs Bone Development via Disturbances in the OC/Leptin and RANKL/RANK/OPG Systems in Weaned Rat Offspring
Ewa Tomaszewska, Halyna Rudyk, Siemowit Muszyński, et al.
Journal of Inherited Metabolic Disease
|
May 19, 2010
High-resolution melting analysis, a simple and effective method for reliable mutation scanning and frequency studies in the ACADVL gene
Rikke Katrine Jentoft Olsen, Steven F Dobrowolski, Margrethe Kjeldsen, et al.
Molecular Genetics and Metabolism
|
May 21, 2015
Altered DNA methylation in PAH deficient phenylketonuria
Steven F Dobrowolski, James Lyons-Weiler, Kayla Spridik, et al.
The EMBO Journal
|
October 1, 1991
The GTPase stimulatory activities of the neurofibromatosis type 1 and the yeast IRA2 proteins are inhibited by arachidonic acid
M Golubić, K Tanaka, S Dobrowolski, et al.
Journal of Inherited Metabolic Disease
|
October 22, 2008
Biochemical characterization of mutant phenylalanine hydroxylase enzymes and correlation with clinical presentation in hyperphenylalaninaemic patients
S F Dobrowolski, A L Pey, R Koch, et al.
Journal of the American Society of Nephrology : JASN
|
May 21, 2011
The connexin 40 A96S mutation causes renin-dependent hypertension
Indra Lübkemeier, Katharina Machura, Lisa Kurtz, et al.
Page
of 102
Search research articles
Search
Showing results (671-680 of 1,014) with videos related to
Sort By:
Page
of 102
Molecular Genetics and Metabolism
|
May 21, 2024
A multiomics approach reveals evidence for phenylbutyrate as a potential treatment for combined D,L-2- hydroxyglutaric aciduria
Yu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
The Journal of Physical Chemistry. A
|
August 5, 2017
Chiral Thiophene Sulfonamide-A Challenge for VOA Calculations
Joanna E Rode, Jan Cz Dobrowolski, Krzysztof Lyczko, et al.
Biorxiv : the Preprint Server for Biology
|
February 13, 2023
A multiomics approach to understanding pathology of Combined D,L-2- Hydroxyglutaric Aciduria and phenylbutyrate as potential treatment
Yu Leng Phua, Olivia M D'Annibale, Anuradha Karunanidhi, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
September 12, 2025
Concentrations of adrenocorticotropic hormone too low to effect cortisol enhance osteogenesis in vitro and in vivo
Irina L Tourkova, Reed A Rankin, Quitterie C Larrouture, et al.
International Journal of Molecular Sciences
|
May 27, 2023
Prenatal Fumonisin Exposure Impairs Bone Development via Disturbances in the OC/Leptin and RANKL/RANK/OPG Systems in Weaned Rat Offspring
Ewa Tomaszewska, Halyna Rudyk, Siemowit Muszyński, et al.
Journal of Inherited Metabolic Disease
|
May 19, 2010
High-resolution melting analysis, a simple and effective method for reliable mutation scanning and frequency studies in the ACADVL gene
Rikke Katrine Jentoft Olsen, Steven F Dobrowolski, Margrethe Kjeldsen, et al.
Molecular Genetics and Metabolism
|
May 21, 2015
Altered DNA methylation in PAH deficient phenylketonuria
Steven F Dobrowolski, James Lyons-Weiler, Kayla Spridik, et al.
The EMBO Journal
|
October 1, 1991
The GTPase stimulatory activities of the neurofibromatosis type 1 and the yeast IRA2 proteins are inhibited by arachidonic acid
M Golubić, K Tanaka, S Dobrowolski, et al.
Journal of Inherited Metabolic Disease
|
October 22, 2008
Biochemical characterization of mutant phenylalanine hydroxylase enzymes and correlation with clinical presentation in hyperphenylalaninaemic patients
S F Dobrowolski, A L Pey, R Koch, et al.
Journal of the American Society of Nephrology : JASN
|
May 21, 2011
The connexin 40 A96S mutation causes renin-dependent hypertension
Indra Lübkemeier, Katharina Machura, Lisa Kurtz, et al.
Page
of 102