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Biochemical and Biophysical Research Communications|March 4, 2010
Establishment of a novel monoclonal antibody against LGR5Yuka Sasaki, Hiromichi Kosaka, Katsuaki Usami, et al.
American Journal of Medical Genetics. Part A|February 24, 2025
Clinical and Molecular Genetic Analyses of a Girl With Isolated Nephrogenic Diabetes Insipidus due to Contiguous Gene Deletion Involving AVPR2 and L1CAMShoma Saito, Shigeru Suzuki, Kengo Izumi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 24, 2014
HbA1c can be a useful glycemic control marker for patients with neonatal diabetes mellitus older than 20 weeks of ageAkiko Furuya, Shigeru Suzuki, Masafumi Koga, et al.
Molecular and Cellular Biology|October 16, 2003
Identification of NAP1, a regulatory subunit of IkappaB kinase-related kinases that potentiates NF-kappaB signalingFumitaka Fujita, Yuko Taniguchi, Takashi Kato, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 5, 2014
Glycemic control and motor development in a patient with intermediate DENDHideharu Oka, Shigeru Suzuki, Akiko Furuya, et al.
Biochemical and Biophysical Research Communications|November 1, 2003
Posttranscriptional regulation of human ABCA7 and its function for the apoA-I-dependent lipid releaseYuika Ikeda, Sumiko Abe-Dohmae, Youichi Munehira, et al.
Annals of Clinical Biochemistry|May 16, 2015
Age-adjusted glycated albumin accurately reflects blood glucose in patients with neonatal diabetes mellitus: comparison with calculated glycated albumin determined by past blood glucose concentrationsShigeru Suzuki, Akiko Furuya, Miho Oshima, et al.
Journal of Clinical Laboratory Analysis|May 26, 2012
New sandwich-type enzyme-linked immunosorbent assay for human MxA protein in a whole blood using monoclonal antibodies against GTP-binding domain for recognition of viral infectionMizuho Kawamura, Akira Kusano, Akiko Furuya, et al.
European Journal of Medical Genetics|August 18, 2020
A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variationShigeru Suzuki, Takahide Kokumai, Akiko Furuya, et al.
European Journal of Endocrinology|April 22, 2021
A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expressionShigeru Suzuki, Kumihiro Matsuo, Yoshiya Ito, et al.
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