FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

REGISTER

now for free

R Sakuma

Research Profile

Chemicals & Drugs

Disorders

Physiology

Anatomy

B-Lymphocytes

Genes & Molecular Sequences

Amino Acid Sequences

Concepts & Ideas

Molecular Sequence Data

Living Beings

Nuclear Family

Register to see full profile

Co-author Network

Register to see all co-authors

Publications

TOP 3
Kimiyoshi Ichida; T Matsumura; R Sakuma; Tatsuo Hosoya; T Nishino
Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II.
Miho Hikita; Tatsuo Hosoya; Kimiyoshi Ichida; Hideaki Okabe; M Saji; Iwao Ohno; Satoru Kuriyama; Haruo Tomonari; F Hayashi; Kenji Onouchi; Shin Fujimori; N Yamaoka; R Sakuma
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase manifesting as acute renal damage.
Shin Fujimori; N Yamaoka; R Sakuma; M Hakoda; H Yamanaka; I Akaoka; N Kamatani
A first evidence of an asymptomatic germline missense base substitution in the hypoxanthine phosphoribosyltransferase (HPRT) gene in humans.

Register to see all publications

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Register to see more

Geonetwork of R Sakuma (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Register to see more

All Publications

2001: Kimiyoshi Ichida; T Matsumura; R Sakuma; Tatsuo Hosoya; T Nishino
Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II.
Biochemical and biophysical research communications 2001;282(5):1194-200.
1998: Miho Hikita; Tatsuo Hosoya; Kimiyoshi Ichida; Hideaki Okabe; M Saji; Iwao Ohno; Satoru Kuriyama; Haruo Tomonari; F Hayashi; Kenji Onouchi; Shin Fujimori; N Yamaoka; R Sakuma
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase manifesting as acute renal damage.
Internal medicine (Tokyo, Japan) 1998;37(11):945-9.
1998: Shin Fujimori; N Yamaoka; R Sakuma; M Hakoda; H Yamanaka; I Akaoka; N Kamatani
A first evidence of an asymptomatic germline missense base substitution in the hypoxanthine phosphoribosyltransferase (HPRT) gene in humans.
Advances in experimental medicine and biology 1998;431():319-22.
1998: Kimiyoshi Ichida; M Yoshida; R Sakuma; Tatsuo Hosoya
Two siblings with classical xanthinuria type 1: significance of allopurinol loading test.
Internal medicine (Tokyo, Japan) 1998;37(1):77-82.
1997: Shin Fujimori; R Sakuma; N Yamaoka; M Hakoda; H Yamanaka; N Kamatani
An asymptomatic germline missense base substitution in the hypoxanthine phosphoribosyltransferase (HPRT) gene that reduces the amount of enzyme in humans.
Human genetics 1997;99(1):8-10.

Register to see more

Copyright © 2011 Elsevier Inc. All rights reserved.