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Showing results (581-590 of 589) with videos related to

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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 AncestorsKurt 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 AncestorsKurt 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 allergyA 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 progressionDhanur 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 reefsTyler 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 achalasiaJessica Becker, Stefan Niebisch, Arcangelo Ricchiuto, et al.
Nature Genetics|July 7, 2014
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasiaInes 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 EuropeansJessica Becker, Stephan L Haas, Anna Mokrowiecka, et al.
Pageof 59

Showing results (581-590 of 589) with videos related to

Sort By:
Pageof 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 AncestorsKurt 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 AncestorsKurt 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 allergyA 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 progressionDhanur 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 reefsTyler 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 achalasiaJessica Becker, Stefan Niebisch, Arcangelo Ricchiuto, et al.
Nature Genetics|July 7, 2014
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasiaInes 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 EuropeansJessica Becker, Stephan L Haas, Anna Mokrowiecka, et al.
Pageof 59