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Clinical Calcium
|
February 25, 2017
[Diagnosis for skeletal muscle disorders using next-generation sequencing.]
Satomi Mitsuhashi
Autophagy
|
October 26, 2011
Phospholipid synthetic defect and mitophagy in muscle disease
Satomi Mitsuhashi, Ichizo Nishino
Journal of Human Genetics
|
September 28, 2019
Long-read sequencing for rare human genetic diseases
Satomi Mitsuhashi, Naomichi Matsumoto
Current Opinion in Neurology
|
August 16, 2013
Megaconial congenital muscular dystrophy due to loss-of-function mutations in choline kinase β
Satomi Mitsuhashi, Ichizo Nishino
Seminars in Pediatric Neurology
|
December 19, 2012
Update on the genetics of limb girdle muscular dystrophy
Satomi Mitsuhashi, Peter B Kang
Methods in Molecular Biology (Clifton, N.J.)
|
February 13, 2023
Analysis of Tandem Repeat Expansions Using Long DNA Reads
Satomi Mitsuhashi, Martin C Frith
Methods in Molecular Biology (Clifton, N.J.)
|
February 13, 2023
Finding Rearrangements in Nanopore DNA Reads with LAST and dnarrange
Martin C Frith, Satomi Mitsuhashi
BMC Medical Genomics
|
January 8, 2021
Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general population
Satomi Mitsuhashi, Martin C Frith, Naomichi Matsumoto
Methods in Molecular Biology (Clifton, N.J.)
|
December 8, 2020
lamassemble: Multiple Alignment and Consensus Sequence of Long Reads
Martin C Frith, Satomi Mitsuhashi, Kazutaka Katoh
Journal of Medical Genetics
|
September 8, 2016
Targeted massively parallel sequencing and histological assessment of skeletal muscles for the molecular diagnosis of inherited muscle disorders
Atsuko Nishikawa, Satomi Mitsuhashi, Naomasa Miyata, et al.
Page
of 14
Search research articles
Search
Showing results (1-10 of 132) with videos related to
Sort By:
Page
of 14
Clinical Calcium
|
February 25, 2017
[Diagnosis for skeletal muscle disorders using next-generation sequencing.]
Satomi Mitsuhashi
Autophagy
|
October 26, 2011
Phospholipid synthetic defect and mitophagy in muscle disease
Satomi Mitsuhashi, Ichizo Nishino
Journal of Human Genetics
|
September 28, 2019
Long-read sequencing for rare human genetic diseases
Satomi Mitsuhashi, Naomichi Matsumoto
Current Opinion in Neurology
|
August 16, 2013
Megaconial congenital muscular dystrophy due to loss-of-function mutations in choline kinase β
Satomi Mitsuhashi, Ichizo Nishino
Seminars in Pediatric Neurology
|
December 19, 2012
Update on the genetics of limb girdle muscular dystrophy
Satomi Mitsuhashi, Peter B Kang
Methods in Molecular Biology (Clifton, N.J.)
|
February 13, 2023
Analysis of Tandem Repeat Expansions Using Long DNA Reads
Satomi Mitsuhashi, Martin C Frith
Methods in Molecular Biology (Clifton, N.J.)
|
February 13, 2023
Finding Rearrangements in Nanopore DNA Reads with LAST and dnarrange
Martin C Frith, Satomi Mitsuhashi
BMC Medical Genomics
|
January 8, 2021
Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general population
Satomi Mitsuhashi, Martin C Frith, Naomichi Matsumoto
Methods in Molecular Biology (Clifton, N.J.)
|
December 8, 2020
lamassemble: Multiple Alignment and Consensus Sequence of Long Reads
Martin C Frith, Satomi Mitsuhashi, Kazutaka Katoh
Journal of Medical Genetics
|
September 8, 2016
Targeted massively parallel sequencing and histological assessment of skeletal muscles for the molecular diagnosis of inherited muscle disorders
Atsuko Nishikawa, Satomi Mitsuhashi, Naomasa Miyata, et al.
Page
of 14