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Human Molecular Genetics
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January 2, 2015
Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly
Katia Hardies, Patrick May, Tania Djémié, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 24, 2021
Replication of a Novel Parkinson's Locus in a European Ancestry Population
Sandeep Grover, Ashwin Ashok Kumar-Sreelatha, Dheeraj R Bobbili, et al.
Nature Methods
|
May 14, 2013
High-throughput tetrad analysis
Catherine L Ludlow, Adrian C Scott, Gareth A Cromie, et al.
The ISME Journal
|
July 19, 2023
Spatio-functional organization in virocells of small uncultivated archaea from the deep biosphere
Indra Banas, Sarah P Esser, Victoria Turzynski, et al.
Nature Ecology & Evolution
|
November 13, 2023
Forecasting the dynamics of a complex microbial community using integrated meta-omics
Francesco Delogu, Benoit J Kunath, Pedro M Queirós, et al.
G3 (Bethesda, Md.)
|
October 15, 2013
Genomic sequence diversity and population structure of Saccharomyces cerevisiae assessed by RAD-seq
Gareth A Cromie, Katie E Hyma, Catherine L Ludlow, et al.
Nature Microbiology
|
October 11, 2016
Integrated multi-omics of the human gut microbiome in a case study of familial type 1 diabetes
Anna Heintz-Buschart, Patrick May, Cédric C Laczny, et al.
Nature Microbiology
|
October 25, 2016
Erratum: Integrated multi-omics of the human gut microbiome in a case study of familial type 1 diabetes
Anna Heintz-Buschart, Patrick May, Cédric C Laczny, et al.
BMC Biology
|
May 16, 2018
Small RNA profiling of low biomass samples: identification and removal of contaminants
Anna Heintz-Buschart, Dilmurat Yusuf, Anne Kaysen, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects
Carla Marini, Katia Hardies, Tiziana Pisano, et al.
Page
of 21
Search research articles
Search
Showing results (111-120 of 209) with videos related to
Sort By:
Page
of 21
Human Molecular Genetics
|
January 2, 2015
Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly
Katia Hardies, Patrick May, Tania Djémié, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 24, 2021
Replication of a Novel Parkinson's Locus in a European Ancestry Population
Sandeep Grover, Ashwin Ashok Kumar-Sreelatha, Dheeraj R Bobbili, et al.
Nature Methods
|
May 14, 2013
High-throughput tetrad analysis
Catherine L Ludlow, Adrian C Scott, Gareth A Cromie, et al.
The ISME Journal
|
July 19, 2023
Spatio-functional organization in virocells of small uncultivated archaea from the deep biosphere
Indra Banas, Sarah P Esser, Victoria Turzynski, et al.
Nature Ecology & Evolution
|
November 13, 2023
Forecasting the dynamics of a complex microbial community using integrated meta-omics
Francesco Delogu, Benoit J Kunath, Pedro M Queirós, et al.
G3 (Bethesda, Md.)
|
October 15, 2013
Genomic sequence diversity and population structure of Saccharomyces cerevisiae assessed by RAD-seq
Gareth A Cromie, Katie E Hyma, Catherine L Ludlow, et al.
Nature Microbiology
|
October 11, 2016
Integrated multi-omics of the human gut microbiome in a case study of familial type 1 diabetes
Anna Heintz-Buschart, Patrick May, Cédric C Laczny, et al.
Nature Microbiology
|
October 25, 2016
Erratum: Integrated multi-omics of the human gut microbiome in a case study of familial type 1 diabetes
Anna Heintz-Buschart, Patrick May, Cédric C Laczny, et al.
BMC Biology
|
May 16, 2018
Small RNA profiling of low biomass samples: identification and removal of contaminants
Anna Heintz-Buschart, Dilmurat Yusuf, Anne Kaysen, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects
Carla Marini, Katia Hardies, Tiziana Pisano, et al.
Page
of 21