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Showing results (961-970 of 1,005) with videos related to

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International Journal for Parasitology. Drugs and Drug Resistance|December 18, 2014
Recent advances in candidate-gene and whole-genome approaches to the discovery of anthelmintic resistance markers and the description of drug/receptor interactionsAndrew C Kotze, Peter W Hunt, Philip Skuce, et al.
Human Mutation|June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variantsDuyen H Pham, Melissa R Pitman, Raman Kumar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 30, 2025
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformationIne Hoogwijs, Simone A Mandelstam, George McGillivray, et al.
Brain : a Journal of Neurology|December 18, 2025
A functional role for septin-2 in the maintenance of the axon initial segment and in human cognitive developmentLuisa Weiss, Macarena Pavez, Anastasia Labudina, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 11, 2023
Risk of COVID-19 in people with multiple sclerosis who are seronegative following vaccinationSafiya A Zaloum, Callum H Wood, Pooja Tank, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Genes and Immunity|June 25, 2010
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosisM Ban, J L McCauley, R Zuvich, et al.
The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
Nature Genetics|February 2, 2000
Aberrant CpG-island methylation has non-random and tumour-type-specific patternsJ F Costello, M C Frühwald, D J Smiraglia, et al.
Nature Genetics|December 17, 2008
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesisZandra A Jenkins, Margriet van Kogelenberg, Tim Morgan, et al.
Pageof 101

Showing results (961-970 of 1,005) with videos related to

Sort By:
Pageof 101
International Journal for Parasitology. Drugs and Drug Resistance|December 18, 2014
Recent advances in candidate-gene and whole-genome approaches to the discovery of anthelmintic resistance markers and the description of drug/receptor interactionsAndrew C Kotze, Peter W Hunt, Philip Skuce, et al.
Human Mutation|June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variantsDuyen H Pham, Melissa R Pitman, Raman Kumar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 30, 2025
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformationIne Hoogwijs, Simone A Mandelstam, George McGillivray, et al.
Brain : a Journal of Neurology|December 18, 2025
A functional role for septin-2 in the maintenance of the axon initial segment and in human cognitive developmentLuisa Weiss, Macarena Pavez, Anastasia Labudina, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 11, 2023
Risk of COVID-19 in people with multiple sclerosis who are seronegative following vaccinationSafiya A Zaloum, Callum H Wood, Pooja Tank, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Genes and Immunity|June 25, 2010
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosisM Ban, J L McCauley, R Zuvich, et al.
The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
Nature Genetics|February 2, 2000
Aberrant CpG-island methylation has non-random and tumour-type-specific patternsJ F Costello, M C Frühwald, D J Smiraglia, et al.
Nature Genetics|December 17, 2008
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesisZandra A Jenkins, Margriet van Kogelenberg, Tim Morgan, et al.
Pageof 101