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Medrxiv : the Preprint Server for Health Sciences
|
October 7, 2024
Plasma glucosylceramide levels are regulated by <i>ATP10D</i> and are not involved in Parkinson's disease pathogenesis
Emma N Somerville, Alva James, Christian Beetz, et al.
International Journal of Molecular Sciences
|
April 23, 2022
The Inhibitory Response to PI3K/AKT Pathway Inhibitors MK-2206 and Buparlisib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines
Yixuan Ma, Sina Sender, Anett Sekora, et al.
Plos One
|
June 1, 2013
Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies
Darina Czamara, Carla M T Tiesler, Gabriele Kohlböck, et al.
International Journal of Molecular Sciences
|
April 23, 2022
Inhibitory Response to CK II Inhibitor Silmitasertib and CDKs Inhibitor Dinaciclib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines
Yixuan Ma, Sina Sender, Anett Sekora, et al.
The American Journal of Clinical Nutrition
|
October 14, 2016
To eat or not to eat? Indicators for reduced food intake in 91,245 patients hospitalized on nutritionDays 2006-2014 in 56 countries worldwide: a descriptive analysis
Karin Schindler, Michael Themessl-Huber, Michael Hiesmayr, et al.
Plos One
|
May 26, 2012
FADS1 FADS2 gene cluster, PUFA intake and blood lipids in children: results from the GINIplus and LISAplus studies
Marie Standl, Eva Lattka, Barbara Stach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 18, 2012
Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients
Vinko Palada, Sandra Stiern, Nicola Glöckle, et al.
Neurology
|
June 19, 2016
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families
Anne S Soehn, Tim W Rattay, Stefanie Beck-Wödl, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2025
Beyond genomics: using RNA-seq from dried blood spots to unlock the clinical relevance of splicing variation in a diagnostic setting
Aida M Bertoli-Avella, Mandy Radefeldt, Ruslan Al-Ali, et al.
Nano Letters
|
February 1, 2013
Tuning the magnetic properties of metal oxide nanocrystal heterostructures by cation exchange
Mykhailo Sytnyk, Raimund Kirchschlager, Maryna I Bodnarchuk, et al.
Page
of 59
Search research articles
Search
Showing results (361-370 of 585) with videos related to
Sort By:
Page
of 59
Medrxiv : the Preprint Server for Health Sciences
|
October 7, 2024
Plasma glucosylceramide levels are regulated by <i>ATP10D</i> and are not involved in Parkinson's disease pathogenesis
Emma N Somerville, Alva James, Christian Beetz, et al.
International Journal of Molecular Sciences
|
April 23, 2022
The Inhibitory Response to PI3K/AKT Pathway Inhibitors MK-2206 and Buparlisib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines
Yixuan Ma, Sina Sender, Anett Sekora, et al.
Plos One
|
June 1, 2013
Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies
Darina Czamara, Carla M T Tiesler, Gabriele Kohlböck, et al.
International Journal of Molecular Sciences
|
April 23, 2022
Inhibitory Response to CK II Inhibitor Silmitasertib and CDKs Inhibitor Dinaciclib Is Related to Genetic Differences in Pancreatic Ductal Adenocarcinoma Cell Lines
Yixuan Ma, Sina Sender, Anett Sekora, et al.
The American Journal of Clinical Nutrition
|
October 14, 2016
To eat or not to eat? Indicators for reduced food intake in 91,245 patients hospitalized on nutritionDays 2006-2014 in 56 countries worldwide: a descriptive analysis
Karin Schindler, Michael Themessl-Huber, Michael Hiesmayr, et al.
Plos One
|
May 26, 2012
FADS1 FADS2 gene cluster, PUFA intake and blood lipids in children: results from the GINIplus and LISAplus studies
Marie Standl, Eva Lattka, Barbara Stach, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 18, 2012
Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients
Vinko Palada, Sandra Stiern, Nicola Glöckle, et al.
Neurology
|
June 19, 2016
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families
Anne S Soehn, Tim W Rattay, Stefanie Beck-Wödl, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2025
Beyond genomics: using RNA-seq from dried blood spots to unlock the clinical relevance of splicing variation in a diagnostic setting
Aida M Bertoli-Avella, Mandy Radefeldt, Ruslan Al-Ali, et al.
Nano Letters
|
February 1, 2013
Tuning the magnetic properties of metal oxide nanocrystal heterostructures by cation exchange
Mykhailo Sytnyk, Raimund Kirchschlager, Maryna I Bodnarchuk, et al.
Page
of 59