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American Journal of Medical Genetics|June 13, 1997
Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese familyN Takamura, I Hombrados, K Tanigawa, et al.
Human Genetics|May 1, 1996
A novel point mutation in congenital erythropoietic porphyria in two members of Japanese familyK Tanigawa, M Bensidhoum, N Takamura, et al.
The Journal of Clinical Endocrinology and Metabolism|July 15, 1999
Prop-1 gene expression in human pituitary tumorsS Nakamura, A Ohtsuru, N Takamura, et al.
AJR. American Journal of Roentgenology|February 5, 2000
MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutationsO Fofanova, N Takamura, E Kinoshita, et al.
Endocrine Journal|January 16, 2002
Urinary iodine levels and thyroid diseases in children; comparison between Nagasaki and ChernobylK Ishigaki, H Namba, N Takamura, et al.
Endocrine Journal|April 1, 1995
A single missense mutation in codon 918 of the RET proto-oncogene in sporadic medullary thyroid carcinomasS Maeda, H Namba, N Takamura, et al.
Thyroid : Official Journal of the American Thyroid Association|September 11, 1999
Developmental and hormonal regulation of thermosensitive neuron potential activity in rat brainS Belugin, K Akino, N Takamura, et al.
Endocrinology|March 10, 1998
Expression profile of receptor-type protein tyrosine kinase genes in the human thyroidK Tanaka, Y Nagayama, T Nakano, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|January 26, 2016
Radioactive Doses - Predicted and Actual - and Likely Health EffectsS Nagataki, N Takamura
Endocrinology|March 31, 1999
Thyrotropin regulates c-Jun N-terminal kinase (JNK) activity through two distinct signal pathways in human thyroid cellsT Hara, H Namba, N Takamura, et al.
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