M. Yanazawa

发表

Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation

E. Zackai, Soma Das, A. Toutain, 2004, Human mutation.

Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism.

S. Miyagawa-Tomita, M. Yokoyama, H. Ohuchi, 1999, Development.

Expression of inhibin α-subunit gene during mouse gametogenesis

M. Yanazawa, H. Fujimoto, S. Toné, 1990 .

Analysis of Embryonic Chick Periderm by Monoclonal Antibody Specific against Periderm 1

K. Kitamura, M. Yanazawa, M. Sezaki, 1990 .

Feather buds exert a polarizing activity when transplanted to chick limb buds

A. Kuroiwa, K. Kitamura, M. Yanazawa, 1996, Development, growth & differentiation.

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

W. Dobyns, M. Kusaka, I. Kondo, 2002, Nature Genetics.

Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.

Y. Yanagawa, Kenji Nakamura, Rika Suzuki-Migishima, 2009, Human molecular genetics.

Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation

Kentaro Kato, T. Miyashita, K. Kitamura, 1997, Mechanisms of Development.

Arx homeobox gene is essential for development of mouse olfactory system

Y. Yoshihara, K. Kitamura, M. Yanazawa, 2005, Development.

Na, K-ATPase α3 is a death target of Alzheimer patient amyloid-β assembly

M. Hagiwara, A. Kakita, D. Teplow, 2015, Proceedings of the National Academy of Sciences.

Isolation and Characterization of Patient-derived, Toxic, High Mass Amyloid β-Protein (Aβ) Assembly from Alzheimer Disease Brains*

K. Imahori, A. Kakita, D. Teplow, 2009, The Journal of Biological Chemistry.

Expression of a novel aristaless related homeobox gene ‘Arx’ in the vertebrate telencephalon, diencephalon and floor plate

Kentaro Kato, K. Kitamura, M. Yanazawa, 1997, Mechanisms of Development.

Isolation and Characterization of Patient-derived, Toxic, High Mass Amyloid β-Protein (Aβ) Assembly from Alzheimer Disease Brains*

K. Imahori, A. Kakita, D. Teplow, 2009, The Journal of Biological Chemistry.

Isolation and Characterization of Patient-derived, Toxic, High Mass Amyloid (cid:1) -Protein (A (cid:1) ) Assembly from Alzheimer Disease Brains

K. Imahori, A. Kakita, D. Teplow, 2009 .

Na, K-ATPase α3 is a death target of Alzheimer patient amyloid-β assembly

M. Hagiwara, A. Kakita, D. Teplow, 2015, Proceedings of the National Academy of Sciences.