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Annals of Human Genetics
|
July 25, 2013
Spinal muscular atrophy: from gene discovery to clinical trials
Dian 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 DNA
Mawaddah 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 Analysis
Yogik 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 Patients
Mawaddah 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 Differentiation
Yoshihisa 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) patients
Tomoto 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, Japan
Yoriko 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 population
Surini 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>, 2110
Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
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Showing results (91-100 of 99) with videos related to
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Page
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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 trials
Dian 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 DNA
Mawaddah 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 Analysis
Yogik 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 Patients
Mawaddah 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 Differentiation
Yoshihisa 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) patients
Tomoto 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, Japan
Yoriko 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 population
Surini 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>, 2110
Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, et al.
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