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Leukemia Research|January 23, 2009
Chemo-sensitivity in a panel of B-cell precursor acute lymphoblastic leukemia cell lines, YCUB series, derived from childrenHiroaki Goto, Takuya Naruto, Reo Tanoshima, et al.
Journal of Dermatological Science|March 27, 2017
Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndromeYoshihiro Matsudate, Takuya Naruto, Yumiko Hayashi, et al.
Modern Rheumatology|September 26, 2008
Methotrexate for the treatment of juvenile idiopathic arthritis: process to approval for JIA indication in JapanMasaaki Mori, Takuya Naruto, Tomoyuki Imagawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 12, 2009
Soluble tumor necrosis factor receptor-1 in preterm infants with chronic lung diseaseMiho Sato, Masaaki Mori, Shigeru Nishimaki, et al.
Vaccine|July 12, 2005
A CpG-containing oligodeoxynucleotide as an efficient adjuvant counterbalancing the Th1/Th2 immune response in diphtheria-tetanus-pertussis vaccineToshiyuki Sugai, Masaaki Mori, Masatoshi Nakazawa, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
A 590 kb deletion caused by non-allelic homologous recombination between two LINE-1 elements in a patient with mesomelia-synostosis syndromeTomohiro Kohmoto, Takuya Naruto, Miki Watanabe, et al.
Journal of Medical Genetics|May 24, 2025
Genotype-phenotype correlations and phenotypic expansion in a case series of ReNU syndrome associated with RNU4-2 variantsYukiko Kuroda, Koki Nagai, Yasuhiro Kawai, et al.
American Journal of Medical Genetics. Part A|January 19, 2016
A unique TBX5 microdeletion with microinsertion detected in patient with Holt-Oram syndromeMikio Morine, Tomohiro Kohmoto, Kiyoshi Masuda, et al.
American Journal of Medical Genetics. Part A|December 23, 2022
Complex congenital cardiovascular anomaly in a patient with AGO1-associated disorderMinako Takagi, Shin Ono, Tatsuro Kumaki, et al.
Human Genome Variation|June 15, 2018
Biallelic mutations of EGFR in a compound heterozygous state cause ectodermal dysplasia with severe skin defects and gastrointestinal dysfunctionShion Hayashi, Takayuki Yokoi, Chihiro Hatano, et al.
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