Lista de obras -

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

artículo científico publicado en 2017

A series of maturity onset diabetes of the young, type 2 (MODY2) mouse models generated by a large-scale ENU mutagenesis program

artículo científico publicado en 2004

Assembly of the cochlear gap junction macromolecular complex requires connexin 26.

artículo científico publicado en 2014

Autoimmune disorders associated with gain of function of the intracellular sensor MDA5.

artículo científico publicado en 2014

Brn-1 and Brn-2 share crucial roles in the production and positioning of mouse neocortical neurons

scientific journal article

Carcinogenicity of dimethylarsinic acid in Ogg1-deficient mice

scientific article published on 18 April 2007

Cell proliferation in liver of Mmh/Ogg1-deficient mice enhances mutation frequency because of the presence of 8-hydroxyguanine in DNA

scientific journal article

Corrigendum: Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

scientific article published on 01 July 2019

Crucial roles of Brn1 in distal tubule formation and function in mouse kidney

scientific journal article

Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness

artículo científico publicado en 2014

Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice

artículo científico publicado en 2015

Development and implementation of a database system to manage a large-scale mouse ENU-mutagenesis program

artículo científico publicado en 2004

High accumulation of oxidative DNA damage, 8-hydroxyguanine, in Mmh/Ogg1 deficient mice by chronic oxidative stress.

artículo científico publicado en 2002

Identification of Reliable Components in Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS): a Data-Driven Approach across Metabolic Processes

artículo científico publicado en 2015

Implementation of the modified-SHIRPA protocol for screening of dominant phenotypes in a large-scale ENU mutagenesis program

artículo científico publicado en 2005

Introduction to the Japan Mouse Clinic at the RIKEN BioResource Center

artículo científico publicado en 2009

In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea

artículo científico publicado en 2016

Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses

artículo científico publicado en 2002

Molecular characterization of ENU mouse mutagenesis and archives

artículo científico publicado en 2005

Mouse models for ROS1-fusion-positive lung cancers and their application to the analysis of multikinase inhibitor efficiency.

artículo científico publicado en 2016

Novel allelic mutations in murine Serca2 induce differential development of squamous cell tumors.

artículo científico publicado en 2016

Novel mouse model for Gardner syndrome generated by a large‐scale N‐ethyl‐N‐nitrosourea mutagenesis program ⬇️

artículo científico publicado el 18 de mayo de 2013

Novel retinoblastoma mutation abrogating the interaction to E2F2/3, but not E2F1, led to selective suppression of thyroid tumors

artículo científico publicado en 2014

Nuclear magnetic resonance studies on calmodulin: calcium-dependent spectral change of proteolytic fragments

scientific article published in 1984

Osteoporotic bone formation in mice lacking tob2; involvement of Tob2 in RANK ligand expression and osteoclasts differentiation

scientific journal article

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

artículo científico publicado en 2015

Role of CCK-A receptor for pancreatic function in mice: a study in CCK-A receptor knockout mice

artículo científico publicado en 2002

SDOP-DB: a comparative standardized-protocol database for mouse phenotypic analyses

artículo científico publicado en 2010

The study using wild-type and Ogg1 knockout mice exposed to potassium bromate shows no tumor induction despite an extensive accumulation of 8-hydroxyguanine in kidney DNA.

artículo científico publicado en 2006

Lista de obras de

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

A series of maturity onset diabetes of the young, type 2 (MODY2) mouse models generated by a large-scale ENU mutagenesis program

Assembly of the cochlear gap junction macromolecular complex requires connexin 26.

Autoimmune disorders associated with gain of function of the intracellular sensor MDA5.

Brn-1 and Brn-2 share crucial roles in the production and positioning of mouse neocortical neurons

Carcinogenicity of dimethylarsinic acid in Ogg1-deficient mice

Cell proliferation in liver of Mmh/Ogg1-deficient mice enhances mutation frequency because of the presence of 8-hydroxyguanine in DNA

Corrigendum: Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

Crucial roles of Brn1 in distal tubule formation and function in mouse kidney

Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness

Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice

Development and implementation of a database system to manage a large-scale mouse ENU-mutagenesis program

High accumulation of oxidative DNA damage, 8-hydroxyguanine, in Mmh/Ogg1 deficient mice by chronic oxidative stress.

Identification of Reliable Components in Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS): a Data-Driven Approach across Metabolic Processes

Implementation of the modified-SHIRPA protocol for screening of dominant phenotypes in a large-scale ENU mutagenesis program

Introduction to the Japan Mouse Clinic at the RIKEN BioResource Center

In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea

Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses

Molecular characterization of ENU mouse mutagenesis and archives

Mouse models for ROS1-fusion-positive lung cancers and their application to the analysis of multikinase inhibitor efficiency.

Novel allelic mutations in murine Serca2 induce differential development of squamous cell tumors.

Novel mouse model for Gardner syndrome generated by a large‐scale N‐ethyl‐N‐nitrosourea mutagenesis program ⬇️

Novel retinoblastoma mutation abrogating the interaction to E2F2/3, but not E2F1, led to selective suppression of thyroid tumors

Nuclear magnetic resonance studies on calmodulin: calcium-dependent spectral change of proteolytic fragments

Osteoporotic bone formation in mice lacking tob2; involvement of Tob2 in RANK ligand expression and osteoclasts differentiation

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness

Role of CCK-A receptor for pancreatic function in mice: a study in CCK-A receptor knockout mice

SDOP-DB: a comparative standardized-protocol database for mouse phenotypic analyses

The study using wild-type and Ogg1 knockout mice exposed to potassium bromate shows no tumor induction despite an extensive accumulation of 8-hydroxyguanine in kidney DNA.