Rap1b Is an Effector of Axin2 Regulating Crosstalk of Signaling Pathways During Skeletal Development

Cytosolic proteome profiling of monocytes for male osteoporosis

(2016) W. Zhu et al.   OSTEOPOROSIS INTERNATIONAL

Stem cells of the suture mesenchyme in craniofacial bone development, repair and regeneration

(2016) Takamitsu Maruyama et al.   Nature Communications

Extraembryonic but not embryonic SUMO-specific protease 2 is required for heart development

(2016) Eri O. Maruyama et al.   Scientific Reports

Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition?

(2015) Andrea Accogli et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Skeletal Dysplasias

(2015) Deborah Krakow   CLINICS IN PERINATOLOGY

Rap1 GTPase is required for mouse lens epithelial maintenance and morphogenesis

(2015) Rupalatha Maddala et al.   DEVELOPMENTAL BIOLOGY

Co-opted JNK/SAPK Signaling in Wnt/β-catenin–Induced Tumorigenesis

(2015) Bo Liu et al.   NEOPLASIA

The small GTPase Rap1b negatively regulates neutrophil chemotaxis and transcellular diapedesis by inhibiting Akt activation

(2014) Sachin Kumar et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Disruption of SUMO-Specific Protease 2 Induces Mitochondria Mediated Neurodegeneration

(2014) Jiang Fu et al.   PLoS Genetics

Gpr177 Deficiency Impairs Mammary Development and Prohibits Wnt-Induced Tumorigenesis

(2013) Eri Ohfuchi Maruyama et al.   PLoS One

Gpr177, a novel locus for bone mineral density and osteoporosis, regulates osteogenesis and chondrogenesis in skeletal development

(2012) Takamitsu Maruyama et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Epidermal Wnt Controls Hair Follicle Induction by Orchestrating Dynamic Signaling Crosstalk between the Epidermis and Dermis

(2012) Jiang Fu et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Talin1 and Rap1 Are Critical for Osteoclast Function

(2012) W. Zou et al.   MOLECULAR AND CELLULAR BIOLOGY

Nosology and classification of genetic skeletal disorders: 2010 revision

(2011) Matthew L. Warman et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Rap1 promotes VEGFR2 activation and angiogenesis by a mechanism involving integrin  v 3

(2011) S. Lakshmikanthan et al.   BLOOD

Gpr177/mouse Wntless is essential for Wnt-mediated craniofacial and brain development

(2011) Jiang Fu et al.   DEVELOPMENTAL DYNAMICS

Regulating the regulator: post-translational modification of RAS

(2011) Ian M. Ahearn et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

β-catenin/cyclin D1 mediated development of suture mesenchyme in calvarial morphogenesis

(2010) Anthony J Mirando et al.   BMC DEVELOPMENTAL BIOLOGY

SUMO-specific protease 2 in Mdm2-mediated regulation of p53

(2010) M Jiang et al.   CELL DEATH AND DIFFERENTIATION

BMP signaling in the development of the mouse esophagus and forestomach

(2010) P. Rodriguez et al.   DEVELOPMENT

Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis

(2010) Hsiao-Man Ivy Yu et al.   DEVELOPMENTAL DYNAMICS

The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice

(2010) Matthew B. Greenblatt et al.   JOURNAL OF CLINICAL INVESTIGATION

Fibroblast Growth Factor Receptor Signaling Crosstalk in Skeletogenesis

(2010) H. Miraoui et al.   Science Signaling

The Balance of WNT and FGF Signaling Influences Mesenchymal Stem Cell Fate During Skeletal Development

(2010) T. Maruyama et al.   Science Signaling

Reciprocal regulation of Wnt and Gpr177/mouse Wntless is required for embryonic axis formation

(2009) J. Fu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Specificity in Ras and Rap Signaling

(2008) Judith H. Raaijmakers et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

In VivoTargeted Deletion of Calpain Small Subunit,Capn4,in Cells of the Osteoblast Lineage Impairs Cell Proliferation, Differentiation, and Bone Formation

(2008) Masako Shimada et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

SUMO-Specific Protease 2 Is Essential for Modulating p53-Mdm2 in Development of Trophoblast Stem Cell Niches and Lineages

(2008) Shang-Yi Chiu et al.   PLOS BIOLOGY

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis

(2007) Liangjun Yin et al.   BONE