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Annals of Surgical Oncology
|
August 2, 2020
Validation Study of Fibrinogen and Albumin Score in Esophageal Cancer Patients Who Underwent Esophagectomy: Multicenter Prospective Cohort Study
Satoru Matsuda, Hiroya Takeuchi, Hirofumi Kawakubo, et al.
Microbiology Spectrum
|
February 28, 2024
Vero cell-adapted SARS-CoV-2 strain shows increased viral growth through furin-mediated efficient spike cleavage
Shohei Minami, Tomohiro Kotaki, Yusuke Sakai, et al.
Nature Medicine
|
June 13, 2006
Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency
Antonio M Almeida, Yoshiko Murakami, D Mark Layton, et al.
American Journal of Human Genetics
|
April 9, 2013
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability
Lars Hansen, Hasan Tawamie, Yoshiko Murakami, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 7, 2025
Circulating Tumor DNA Longitudinal Analysis During Total Neoadjuvant Therapy and Non-operative Management for Locally Advanced Rectal Cancer: A Biomarker Study from the NOMINATE Trial
Takashi Akiyoshi, Eiji Shinozaki, Yusuke Maeda, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2021
Hepatitis C virus modulates signal peptide peptidase to alter host protein processing
Junki Hirano, Sachiyo Yoshio, Yusuke Sakai, et al.
American Journal of Human Genetics
|
January 21, 2014
Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation
Malcolm F Howard, Yoshiko Murakami, Alistair T Pagnamenta, et al.
American Journal of Human Genetics
|
July 7, 2009
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies
Dirk J Lefeber, Johannes Schönberger, Eva Morava, et al.
BMJ Open
|
May 31, 2019
Comparison of olanexidine versus povidone-iodine for preventing surgical site infection in gastrointestinal surgery: study protocol for a multicentre, single-blind, randomised controlled clinical trial
Masashi Takeuchi, Hideaki Obara, Hirofumi Kawakubo, et al.
Nature Communications
|
May 28, 2016
ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation
Eric J R Jansen, Sharita Timal, Margret Ryan, et al.
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of 17
Search research articles
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Showing results (151-160 of 161) with videos related to
Sort By:
Page
of 17
Annals of Surgical Oncology
|
August 2, 2020
Validation Study of Fibrinogen and Albumin Score in Esophageal Cancer Patients Who Underwent Esophagectomy: Multicenter Prospective Cohort Study
Satoru Matsuda, Hiroya Takeuchi, Hirofumi Kawakubo, et al.
Microbiology Spectrum
|
February 28, 2024
Vero cell-adapted SARS-CoV-2 strain shows increased viral growth through furin-mediated efficient spike cleavage
Shohei Minami, Tomohiro Kotaki, Yusuke Sakai, et al.
Nature Medicine
|
June 13, 2006
Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency
Antonio M Almeida, Yoshiko Murakami, D Mark Layton, et al.
American Journal of Human Genetics
|
April 9, 2013
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability
Lars Hansen, Hasan Tawamie, Yoshiko Murakami, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 7, 2025
Circulating Tumor DNA Longitudinal Analysis During Total Neoadjuvant Therapy and Non-operative Management for Locally Advanced Rectal Cancer: A Biomarker Study from the NOMINATE Trial
Takashi Akiyoshi, Eiji Shinozaki, Yusuke Maeda, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2021
Hepatitis C virus modulates signal peptide peptidase to alter host protein processing
Junki Hirano, Sachiyo Yoshio, Yusuke Sakai, et al.
American Journal of Human Genetics
|
January 21, 2014
Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation
Malcolm F Howard, Yoshiko Murakami, Alistair T Pagnamenta, et al.
American Journal of Human Genetics
|
July 7, 2009
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies
Dirk J Lefeber, Johannes Schönberger, Eva Morava, et al.
BMJ Open
|
May 31, 2019
Comparison of olanexidine versus povidone-iodine for preventing surgical site infection in gastrointestinal surgery: study protocol for a multicentre, single-blind, randomised controlled clinical trial
Masashi Takeuchi, Hideaki Obara, Hirofumi Kawakubo, et al.
Nature Communications
|
May 28, 2016
ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation
Eric J R Jansen, Sharita Timal, Margret Ryan, et al.
Page
of 17