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Yukari Endo

Showing results (11-20 of 25) with videos related to

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Human Pathology|June 12, 2017
SMARCA4-deficient thoracic sarcoma: report of a case and insights into how to reach the diagnosis using limited samples and resourcesSatoshi Kuwamoto, Michiko Matsushita, Kenichi Takeda, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|June 25, 2019
Plasma Exchange Therapy to Reduce Mortality in Japanese Patients With Diffuse Alveolar Hemorrhage and Microscopic PolyangiitisYoshiyuki Abe, Ken Yamaji, Yukari Endo, et al.
Yonago Acta Medica|May 25, 2023
Construction of an Automatic Quantification Method for Bone Marrow Cellularity Using Image Analysis SoftwareYuki Hatayama, Yukari Endo, Nao Kojima, et al.
Yonago Acta Medica|April 10, 2019
Possible Relationship Between <i>MYBL1</i> Alterations and Specific Primary Sites in Adenoid Cystic Carcinoma: A Clinicopathological and Molecular Study of 36 CasesYukari Endo, Satoshi Kuwamoto, Takahito Ohira, et al.
Yonago Acta Medica|August 26, 2015
Clinical Significance of Microcalcifications Detection in Invasive Breast CarcinomaYuki Hashimoto, Aya Murata, Naoki Miyamoto, et al.
Neurology. Genetics|April 12, 2016
Milder forms of muscular dystrophy associated with POMGNT2 mutationsYukari Endo, Mingrui Dong, Satoru Noguchi, et al.
Elife|April 1, 2020
Identification of drug modifiers for RYR1-related myopathy using a multi-species discovery pipelineJonathan R Volpatti, Yukari Endo, Jessica Knox, et al.
Human Molecular Genetics|November 6, 2023
Two zebrafish cacna1s loss-of-function variants provide models of mild and severe CACNA1S-related myopathyYukari Endo, Linda Groom, Sabrina M Wang, et al.
Human Molecular Genetics|September 18, 2014
Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca²⁺ channelsYukari Endo, Satoru Noguchi, Yuji Hara, et al.
Nature Communications|June 13, 2022
Variants in ASPH cause exertional heat illness and are associated with malignant hyperthermia susceptibilityYukari Endo, Linda Groom, Alper Celik, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Human Pathology|June 12, 2017
SMARCA4-deficient thoracic sarcoma: report of a case and insights into how to reach the diagnosis using limited samples and resourcesSatoshi Kuwamoto, Michiko Matsushita, Kenichi Takeda, et al.
Therapeutic Apheresis and Dialysis : Official Peer-Reviewed Journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy|June 25, 2019
Plasma Exchange Therapy to Reduce Mortality in Japanese Patients With Diffuse Alveolar Hemorrhage and Microscopic PolyangiitisYoshiyuki Abe, Ken Yamaji, Yukari Endo, et al.
Yonago Acta Medica|May 25, 2023
Construction of an Automatic Quantification Method for Bone Marrow Cellularity Using Image Analysis SoftwareYuki Hatayama, Yukari Endo, Nao Kojima, et al.
Yonago Acta Medica|April 10, 2019
Possible Relationship Between <i>MYBL1</i> Alterations and Specific Primary Sites in Adenoid Cystic Carcinoma: A Clinicopathological and Molecular Study of 36 CasesYukari Endo, Satoshi Kuwamoto, Takahito Ohira, et al.
Yonago Acta Medica|August 26, 2015
Clinical Significance of Microcalcifications Detection in Invasive Breast CarcinomaYuki Hashimoto, Aya Murata, Naoki Miyamoto, et al.
Neurology. Genetics|April 12, 2016
Milder forms of muscular dystrophy associated with POMGNT2 mutationsYukari Endo, Mingrui Dong, Satoru Noguchi, et al.
Elife|April 1, 2020
Identification of drug modifiers for RYR1-related myopathy using a multi-species discovery pipelineJonathan R Volpatti, Yukari Endo, Jessica Knox, et al.
Human Molecular Genetics|November 6, 2023
Two zebrafish cacna1s loss-of-function variants provide models of mild and severe CACNA1S-related myopathyYukari Endo, Linda Groom, Sabrina M Wang, et al.
Human Molecular Genetics|September 18, 2014
Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca²⁺ channelsYukari Endo, Satoru Noguchi, Yuji Hara, et al.
Nature Communications|June 13, 2022
Variants in ASPH cause exertional heat illness and are associated with malignant hyperthermia susceptibilityYukari Endo, Linda Groom, Alper Celik, et al.
Pageof 3