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CNP/NPR2 signaling maintains oocyte meiotic arrest in early antral follicles and is suppressed by EGFR-mediated signaling in preovulatory follicles

Molecular reproduction and development, 2012-11, Vol.79 (11), p.795-802

2012

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A Loss-of-Function Mutation in Natriuretic Peptide Receptor 2 (Npr2) Gene Is Responsible for Disproportionate Dwarfism in cn/cn Mouse

The Journal of biological chemistry, 2005-04, Vol.280 (14), p.14288-14292

2005

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NPPC/NPR2 signaling is essential for oocyte meiotic arrest and cumulus oophorus formation during follicular development in the mouse ovary

Reproduction (Cambridge, England), 2012-08, Vol.144 (2), p.187-193

2012

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Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice

PLoS genetics, 2016-12, Vol.12 (12), p.e1006510

2016

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Generation of Evc2/Limbin global and conditional KO mice and its roles during mineralized tissue formation

Genesis (New York, N.Y. : 2000), 2015-09, Vol.53 (9), p.612-626

2015

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Genetic variants of RNF212 involved in meiotic recombination rate and its relation with conception rate in Japanese Black cattle

Dobutsu iden ikushu kenkyu = Journal of animal genetics, 2021, Vol.49 (1), p.13-17

2021

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Non-synonymous FGD3 Variant as Positional Candidate for Disproportional Tall Stature Accounting for a Carcass Weight QTL (CW-3) and Skeletal Dysplasia in Japanese Black Cattle

PLoS genetics, 2015-08, Vol.11 (8), p.e1005433-e1005433

2015

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A missense mutation of the Dhh gene is associated with male pseudohermaphroditic rats showing impaired Leydig cell development

Reproduction (Cambridge, England), 2011-02, Vol.141 (2), p.217-225

2011

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Expression of Evc2 in craniofacial tissues and craniofacial bone defects in Evc2 knockout mouse

Archives of oral biology, 2016-08, Vol.68, p.142-152

2016

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Role of Osteoclast Extracellular Signal‐Regulated Kinase (ERK) in Cell Survival and Maintenance of Cell Polarity

Journal of bone and mineral research, 2003-07, Vol.18 (7), p.1198-1205

2003

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Genetic characterization of Kushum horses in Kazakhstan based on haplotypes of mtDNA and Y chromosome, and genes associated with important traits of the horses

Journal of Equine Science, 2020, Vol.31(3), pp.35-43

2020

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Ellis Van Creveld2 is Required for Postnatal Craniofacial Bone Development

Anatomical record (Hoboken, N.J. : 2007), 2016-08, Vol.299 (8), p.1110-1120

2016

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Gastrointestinal Tract Disorder in Natriuretic Peptide Receptor B Gene Mutant Mice

The American journal of pathology, 2010-08, Vol.177 (2), p.822-828

2010

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Skeletal Analysis of the Long Bone Abnormality (lbab/lbab) Mouse, A Novel Chondrodysplastic C-Type Natriuretic Peptide Mutant

Calcified tissue international, 2012-04, Vol.90 (4), p.307-318

2012

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Hypomorphic mutation in mouse Nppc gene causes retarded bone growth due to impaired endochondral ossification

Biochemical and biophysical research communications, 2008-11, Vol.376 (1), p.186-190

2008

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Reduced Expression of the Endothelin Receptor Type B Gene in Piebald Mice Caused by Insertion of a Retroposon-like Element in Intron 1

The Journal of biological chemistry, 2006-04, Vol.281 (16), p.10799-10807

2006

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A nonsense mutation in mouse Adamtsl2 causes uterine hypoplasia and an irregular estrous cycle

Mammalian genome, 2023-12, Vol.34 (4), p.559-571

2023

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Heparanase Localization during Palatogenesis in Mice

BioMed research international, 2013-01, Vol.2013 (2013), p.1-9

2013

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A mutation of the WFDC1 gene is responsible for multiple ocular defects in cattle

Genomics (San Diego, Calif.), 2009-07, Vol.94 (1), p.55-62

2009

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Characterization of the dwg mutations: dwg and dwg Bayer are new mutant alleles of the Ggt1 gene

Mammalian genome, 2009-12, Vol.20 (11-12), p.711-719

2009

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Association of a non-synonymous variant of MLH3 gene involved in meiotic recombination with conception rate of Japanese Black cattle

Animal production science, 2024-11, Vol.64 (17)

2024

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Characterization of the Skeletal Fusion with Sterility (sks) Mouse Showing Axial Skeleton Abnormalities Caused by Defects of Embryonic Skeletal Development

Experimental Animals, 2014, Vol.63(1), pp.11-19

2014

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Exclusion of NEU1 and PPGB from candidate genes for a lysosomal storage disease in Japanese Black cattle

Animal science journal, 2009-10, Vol.80 (5), p.611-615

2009

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Positional Cloning of the Gene LIMBIN Responsible for Bovine Chondrodysplastic Dwarfism

Proceedings of the National Academy of Sciences - PNAS, 2002-08, Vol.99 (16), p.10549-10554

2002

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Characterization of chromosomal inversion of the mouse hairy ears (Eh) mutation associated with cleft palate

Mammalian genome, 2007-04, Vol.18 (4), p.246-254, Article 246

2007

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CNP/NPR2 signaling maintains oocyte meiotic arrest in early antral follicles and is suppressed by EGFR-mediated signaling in preovulatory follicles

A Loss-of-Function Mutation in Natriuretic Peptide Receptor 2 (Npr2) Gene Is Responsible for Disproportionate Dwarfism in cn/cn Mouse

NPPC/NPR2 signaling is essential for oocyte meiotic arrest and cumulus oophorus formation during follicular development in the mouse ovary

Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice

Generation of Evc2/Limbin global and conditional KO mice and its roles during mineralized tissue formation

Genetic variants of RNF212 involved in meiotic recombination rate and its relation with conception rate in Japanese Black cattle

Non-synonymous FGD3 Variant as Positional Candidate for Disproportional Tall Stature Accounting for a Carcass Weight QTL (CW-3) and Skeletal Dysplasia in Japanese Black Cattle

A missense mutation of the Dhh gene is associated with male pseudohermaphroditic rats showing impaired Leydig cell development

Expression of Evc2 in craniofacial tissues and craniofacial bone defects in Evc2 knockout mouse

Role of Osteoclast Extracellular Signal‐Regulated Kinase (ERK) in Cell Survival and Maintenance of Cell Polarity

Genetic characterization of Kushum horses in Kazakhstan based on haplotypes of mtDNA and Y chromosome, and genes associated with important traits of the horses

Ellis Van Creveld2 is Required for Postnatal Craniofacial Bone Development

Gastrointestinal Tract Disorder in Natriuretic Peptide Receptor B Gene Mutant Mice

Skeletal Analysis of the Long Bone Abnormality (lbab/lbab) Mouse, A Novel Chondrodysplastic C-Type Natriuretic Peptide Mutant

Hypomorphic mutation in mouse Nppc gene causes retarded bone growth due to impaired endochondral ossification

Reduced Expression of the Endothelin Receptor Type B Gene in Piebald Mice Caused by Insertion of a Retroposon-like Element in Intron 1

A nonsense mutation in mouse Adamtsl2 causes uterine hypoplasia and an irregular estrous cycle

Heparanase Localization during Palatogenesis in Mice

A mutation of the WFDC1 gene is responsible for multiple ocular defects in cattle

Characterization of the dwg mutations: dwg and dwg Bayer are new mutant alleles of the Ggt1 gene

Association of a non-synonymous variant of MLH3 gene involved in meiotic recombination with conception rate of Japanese Black cattle

Characterization of the Skeletal Fusion with Sterility (sks) Mouse Showing Axial Skeleton Abnormalities Caused by Defects of Embryonic Skeletal Development

Exclusion of NEU1 and PPGB from candidate genes for a lysosomal storage disease in Japanese Black cattle

Positional Cloning of the Gene LIMBIN Responsible for Bovine Chondrodysplastic Dwarfism

Characterization of chromosomal inversion of the mouse hairy ears (Eh) mutation associated with cleft palate

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