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Experimental Eye Research|October 22, 2002
Non-cleavable mutant Fas ligand transfection of donor cornea abrogates ocular immune privilegeYoichiro Sano, Jun Yamada, Yutaka Ishino, et al.
Pediatric Nephrology (Berlin, Germany)|February 24, 2006
EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditionsMichiyo Okada, Rika Fujimaru, Noriko Morimoto, et al.
Molecular Genetics and Metabolism|May 12, 2020
Pharmacokinetics and pharmacodynamics of JR-051, a biosimilar of agalsidase beta, in healthy adults and patients with Fabry disease: Phase I and II/III clinical studiesKimitoshi Nakamura, Satoshi Kawashima, Hirotaka Tozawa, et al.
Human Genome Variation|September 13, 2022
Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndromeAtsushi Hattori, Torayuki Okuyama, Tetsumin So, et al.
American Journal of Medical Genetics. Part A|September 10, 2005
Segmental and full paternal isodisomy for chromosome 14 in three patients: narrowing the critical region and implication for the clinical featuresMasayo Kagami, Gen Nishimura, Torayuki Okuyama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 15, 2018
Liver transplantation: New treatment for mucopolysaccharidosis type VI in ratsSumika Toyama, Ohsuke Migita, Masayuki Fujino, et al.
Congenital Anomalies|May 31, 2006
Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicismRika Kosaki, Sae Hanai, Hiroki Kakishima, et al.
The Journal of Gene Medicine|November 16, 2004
Inhibition of allogeneic T-cell responses by dendritic cells expressing transduced indoleamine 2,3-dioxygenaseNaoko Funeshima, Masayuki Fujino, Yusuke Kitazawa, et al.
European Journal of Pediatrics|January 12, 2012
Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I RegistryKristin D'Aco, Lisa Underhill, Lakshmi Rangachari, et al.
Molecular Genetics and Metabolism Reports|November 11, 2017
A molecular analysis of the GAA gene and clinical spectrum in 38 patients with Pompe disease in JapanYasuyuki Fukuhara, Naoko Fuji, Narutoshi Yamazaki, et al.
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