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Alzheimer Disease and Associated Disorders
|
November 26, 2024
G2019S Mutation of Leucine-Rich Repeat Kinase 2 Is a Cause of Lewy Body Dementia in Patients With North African Ancestors
Kurt Segers, Florence Benoit, Sophie Levy, et al.
Alzheimer Disease and Associated Disorders
|
August 20, 2025
Erratum: The G2019S Mutation of Leucine-Rich Repeat Kinase 2 is a Cause of Lewy Body Dementia in Patients with North African Ancestors
Kurt Segers, Florence Benoit, Levy Sophie, et al.
Contact Dermatitis
|
June 20, 1998
Genotype and phenotype of N-acetyltransferase 2 (NAT2) polymorphism in patients with contact allergy
A Schnuch, G A Westphal, M M Müller, et al.
Macromolecules
|
March 26, 2026
Examining the Impact of Side-Chain Chirality on Conformation of a Helical Poly(3‑(<i>S</i>‑1-ethylhexyl)esterfuran)
Dhruv Sharma, Manami Kawakami, Megan Rice, et al.
Cell
|
September 27, 2024
mTOR activity paces human blastocyst stage developmental progression
Dhanur P Iyer, Heidar Heidari Khoei, Vera A van der Weijden, et al.
Plos One
|
January 10, 2018
Taking the metabolic pulse of the world's coral reefs
Tyler Cyronak, Andreas J Andersson, Chris Langdon, et al.
European Journal of Gastroenterology & Hepatology
|
February 17, 2016
Comprehensive epidemiological and genotype-phenotype analyses in a large European sample with idiopathic achalasia
Jessica Becker, Stefan Niebisch, Arcangelo Ricchiuto, et al.
Nature Genetics
|
July 7, 2014
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia
Ines Gockel, Jessica Becker, Mira M Wouters, et al.
European Journal of Human Genetics : EJHG
|
January 7, 2016
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Jessica Becker, Stephan L Haas, Anna Mokrowiecka, et al.
Page
of 59
Search research articles
Search
Showing results (581-590 of 589) with videos related to
Sort By:
Page
of 59
You have reached the last page of results.
This site can display upto 589 results.
Alzheimer Disease and Associated Disorders
|
November 26, 2024
G2019S Mutation of Leucine-Rich Repeat Kinase 2 Is a Cause of Lewy Body Dementia in Patients With North African Ancestors
Kurt Segers, Florence Benoit, Sophie Levy, et al.
Alzheimer Disease and Associated Disorders
|
August 20, 2025
Erratum: The G2019S Mutation of Leucine-Rich Repeat Kinase 2 is a Cause of Lewy Body Dementia in Patients with North African Ancestors
Kurt Segers, Florence Benoit, Levy Sophie, et al.
Contact Dermatitis
|
June 20, 1998
Genotype and phenotype of N-acetyltransferase 2 (NAT2) polymorphism in patients with contact allergy
A Schnuch, G A Westphal, M M Müller, et al.
Macromolecules
|
March 26, 2026
Examining the Impact of Side-Chain Chirality on Conformation of a Helical Poly(3‑(<i>S</i>‑1-ethylhexyl)esterfuran)
Dhruv Sharma, Manami Kawakami, Megan Rice, et al.
Cell
|
September 27, 2024
mTOR activity paces human blastocyst stage developmental progression
Dhanur P Iyer, Heidar Heidari Khoei, Vera A van der Weijden, et al.
Plos One
|
January 10, 2018
Taking the metabolic pulse of the world's coral reefs
Tyler Cyronak, Andreas J Andersson, Chris Langdon, et al.
European Journal of Gastroenterology & Hepatology
|
February 17, 2016
Comprehensive epidemiological and genotype-phenotype analyses in a large European sample with idiopathic achalasia
Jessica Becker, Stefan Niebisch, Arcangelo Ricchiuto, et al.
Nature Genetics
|
July 7, 2014
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia
Ines Gockel, Jessica Becker, Mira M Wouters, et al.
European Journal of Human Genetics : EJHG
|
January 7, 2016
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Jessica Becker, Stephan L Haas, Anna Mokrowiecka, et al.
Page
of 59