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Atsuko Takeuchi

Showing results (91-100 of 99) with videos related to

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Annals of Human Genetics|July 25, 2013
Spinal muscular atrophy: from gene discovery to clinical trialsDian K Nurputra, Poh San Lai, Nur Imma F Harahap, et al.
Brain & Development|May 20, 2017
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNAMawaddah Ar Rochmah, Nur Imma Fatimah Harahap, Emma Tabe Eko Niba, et al.
Genetic Testing and Molecular Biomarkers|April 20, 2021
Dried Blood Spot Screening System for Spinal Muscular Atrophy with Allele-Specific Polymerase Chain Reaction and Melting Peak AnalysisYogik Onky Silvana Wijaya, Hisahide Nishio, Emma Tabe Eko Niba, et al.
The Kobe Journal of Medical Sciences|August 21, 2020
Phosphoethanolamine Elevation in Plasma of Spinal Muscular Atrophy Type 1 PatientsMawaddah Ar Rochmah, Yogik Onky Silvana Wijaya, Nur Imma Fatimah Harahap, et al.
ACS Chemical Neuroscience|July 3, 2025
A New Class of Vitamin K Analogues Containing the Side Chain of Retinoic Acid Have Enhanced Activity for Inducing Neuronal DifferentiationYoshihisa Hirota, Taiki Sato, Rina Watanabe, et al.
Brain & Development|December 24, 2013
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patientsTomoto Yamamoto, Hideyuki Sato, Poh San Lai, et al.
Genes|November 24, 2022
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, JapanYoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
Pediatric Research|January 9, 2010
A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay populationSurini Yusoff, Atsuko Takeuchi, Chitose Ashi, et al.
Genes|March 29, 2023
Correction: Noguchi et al. PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. <i>Genes</i> 2022, <i>13</i>, 2110Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
Annals of Human Genetics|July 25, 2013
Spinal muscular atrophy: from gene discovery to clinical trialsDian K Nurputra, Poh San Lai, Nur Imma F Harahap, et al.
Brain & Development|May 20, 2017
Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNAMawaddah Ar Rochmah, Nur Imma Fatimah Harahap, Emma Tabe Eko Niba, et al.
Genetic Testing and Molecular Biomarkers|April 20, 2021
Dried Blood Spot Screening System for Spinal Muscular Atrophy with Allele-Specific Polymerase Chain Reaction and Melting Peak AnalysisYogik Onky Silvana Wijaya, Hisahide Nishio, Emma Tabe Eko Niba, et al.
The Kobe Journal of Medical Sciences|August 21, 2020
Phosphoethanolamine Elevation in Plasma of Spinal Muscular Atrophy Type 1 PatientsMawaddah Ar Rochmah, Yogik Onky Silvana Wijaya, Nur Imma Fatimah Harahap, et al.
ACS Chemical Neuroscience|July 3, 2025
A New Class of Vitamin K Analogues Containing the Side Chain of Retinoic Acid Have Enhanced Activity for Inducing Neuronal DifferentiationYoshihisa Hirota, Taiki Sato, Rina Watanabe, et al.
Brain & Development|December 24, 2013
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patientsTomoto Yamamoto, Hideyuki Sato, Poh San Lai, et al.
Genes|November 24, 2022
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, JapanYoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
Pediatric Research|January 9, 2010
A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay populationSurini Yusoff, Atsuko Takeuchi, Chitose Ashi, et al.
Genes|March 29, 2023
Correction: Noguchi et al. PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. <i>Genes</i> 2022, <i>13</i>, 2110Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
Pageof 10