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Skeletal Analysis of the Long Bone Abnormality ( lbab/ lbab) Mouse, A Novel Chondrodysplastic C-Type Natriuretic Peptide Mutant.
- Published in:
- Calcified Tissue International, 2012, v. 90, n. 4, p. 307, doi. 10.1007/s00223-011-9567-0
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- Article
PCR sexing and developmental rate differences in preimplantation mouse embryos fertilized and cultured in vitro.
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- Molecular Reproduction & Development, 1993, v. 35, n. 2, p. 121, doi. 10.1002/mrd.1080350204
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- Article
Liver transplantation: New treatment for mucopolysaccharidosis type VI in rats.
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- Pediatrics International, 2019, v. 61, n. 2, p. 180, doi. 10.1111/ped.13751
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- Article
Unveiling new perspective of phylogeography, genetic diversity, and population dynamics of Southeast Asian and Pacific chickens.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-18904-3
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- Article
A Mutation in Endothelin-B Receptor Gene Causes Myenteric Aganglionosis and Coat Color Spotting in Rats.
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- DNA Research, 1996, v. 3, n. 2, p. 101, doi. 10.1093/dnares/3.2.101
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- Article
Generation of Evc2/Limbin global and conditional KO mice and its roles during mineralized tissue formation.
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- Genesis: The Journal of Genetics & Development, 2015, v. 53, n. 9, p. 612, doi. 10.1002/dvg.22879
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- Article
Hybrid Sterility with Meiotic Metaphase Arrest in Intersubspecific Mouse Crosses.
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- Journal of Heredity, 2019, v. 11, n. 2, p. 183, doi. 10.1093/jhered/esy060
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- Article
Short-Limbed Dwarfism: slw Is a New Allele of Npr2 Causing Chondrodysplasia.
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- Journal of Heredity, 2007, v. 98, n. 6, p. 575, doi. 10.1093/jhered/esm065
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- Article
Birth of mice from meiotically arrested spermatocytes following biparental meiosis in halved oocytes.
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- EMBO Reports, 2022, v. 23, n. 7, p. 1, doi. 10.15252/embr.202254992
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- Article
Homeobox family Hoxc localization during murine palate formation.
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- Congenital Anomalies, 2016, v. 56, n. 4, p. 172, doi. 10.1111/cga.12153
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- Article
Mutant phenotype analysis suggests potential roles for C-type natriuretic peptide receptor (NPR-B) in male mouse fertility.
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- Reproductive Biology & Endocrinology, 2014, v. 12, n. 1, p. 64, doi. 10.1186/1477-7827-12-64
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- Publication type:
- Article
CNP/NPR2 signaling maintains oocyte meiotic arrest in early antral follicles and is suppressed by EGFR-mediated signaling in preovulatory follicles.
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- Molecular Reproduction & Development, 2012, v. 79, n. 11, p. 795, doi. 10.1002/mrd.22114
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- Publication type:
- Article
Npr2 mutant mice show vasodilation and undeveloped adipocytes in mesentery.
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- BMC Research Notes, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13104-021-05853-9
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- Article
FGF5 and EPAS1 gene polymorphisms are associated with high‐altitude adaptation in Nepalese goat breeds.
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- Animal Science Journal, 2021, v. 92, n. 1, p. 1, doi. 10.1111/asj.13640
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- Article
Distribution of the mutant allele of the DMRT3 gene associated with ambling gaits in Japanese native horse populations.
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- Animal Science Journal, 2020, v. 91, n. 1, p. 1, doi. 10.1111/asj.13431
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- Article
Genetic characterization of Vietnamese Yellow cattle using mitochondrial DNA and Y‐chromosomal haplotypes and genes associated with economical traits.
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- Animal Science Journal, 2018, v. 89, n. 12, p. 1641, doi. 10.1111/asj.13099
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- Article
Genotype distribution and allele frequencies of the genes associated with body composition and locomotion traits in Myanmar native horses.
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- Animal Science Journal, 2017, v. 88, n. 8, p. 1198, doi. 10.1111/asj.12756
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- Article
Low mitochondrial DNA diversity of Japanese Polled and Kuchinoshima feral cattle.
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- Animal Science Journal, 2017, v. 88, n. 5, p. 739, doi. 10.1111/asj.12716
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- Article
Allelic frequencies and association with carcass traits of six genes in local subpopulations of Japanese Black cattle.
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- Animal Science Journal, 2016, v. 87, n. 4, p. 469, doi. 10.1111/asj.12453
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- Article
The assessment of genetic diversity within and among the eight subpopulations of Japanese Black cattle using 52 microsatellite markers.
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- Animal Science Journal, 2013, v. 84, n. 8, p. 585, doi. 10.1111/asj.12045
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- Article
Genetic relationship of body measurement traits at early age with carcass traits in Japanese black cattle.
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- Animal Science Journal, 2013, v. 84, n. 3, p. 206, doi. 10.1111/asj.12005
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- Publication type:
- Article
Genetic variability of maternal effect on body measurements and its intra- and inter-genetic relationship with direct effect in Japanese Black calves.
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- Animal Science Journal, 2012, v. 83, n. 3, p. 199, doi. 10.1111/j.1740-0929.2011.00936.x
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- Article
Exclusion of NEU1 and PPGB from candidate genes for a lysosomal storage disease in Japanese Black cattle.
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- Animal Science Journal, 2009, v. 80, n. 5, p. 611, doi. 10.1111/j.1740-0929.2009.00678.x
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- Article
Marker-assisted selection for forelimb-girdle muscular anomaly of Japanese Black cattle.
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- 2007
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- Publication type:
- Other
Identification of genes responsible for hereditary diseases in Japanese beef cattle.
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- Animal Science Journal, 2005, v. 76, n. 6, p. 525, doi. 10.1111/j.1740-0929.2005.00300.x
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- Article
Polymerase chain reaction-restriction fragment length polymorphism method for identifying carriers of hemophilia A in Japanese brown cattle.
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- Animal Science Journal, 2006, v. 77, n. 1, p. 122, doi. 10.1111/j.1740-0929.2006.00329.x
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- Article
Defective development and microcirculation of intestine in Npr2 mutant mice.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71812-2
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- Article
Ellis Van Creveld2 is Required for Postnatal Craniofacial Bone Development.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2016, v. 299, n. 8, p. 1110, doi. 10.1002/ar.23353
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- Article
Characterization of the dwg mutations: dwg and dwg<sup> Bayer</sup> are new mutant alleles of the Ggt1 gene.
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- Mammalian Genome, 2009, v. 20, n. 11/12, p. 711, doi. 10.1007/s00335-009-9221-6
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- Article
Characterization of chromosomal inversion of the mouse hairy ears ( Eh) mutation associated with cleft palate.
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- Mammalian Genome, 2007, v. 18, n. 4, p. 246, doi. 10.1007/s00335-007-9015-7
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- Article
Linkage mapping of the locus responsible for congenital multiple ocular defects in cattle on bovine Chromosome 18.
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- Mammalian Genome, 2005, v. 16, n. 9, p. 731, doi. 10.1007/s00335-005-0043-x
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- Article
An insertion mutation of the bovine F11 gene is responsible for factor XI deficiency in Japanese black cattle.
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- Mammalian Genome, 2005, v. 16, n. 5, p. 383, doi. 10.1007/s00335-004-2462-5
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- Article
A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene.
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- Mammalian Genome, 2002, v. 13, n. 1, p. 30, doi. 10.1007/s00335-001-3038-2
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- Article
Homozygosity mapping of the locus responsible for renal tubular dysplasia of cattle on bovine Chromosome 1.
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- Mammalian Genome, 2000, v. 11, n. 4, p. 316, doi. 10.1007/s003350010058
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- Publication type:
- Article
Biochemical, Pathological, and Skeletal Improvement of Mucopolysaccharidosis VI After Gene Transfer to Liver but Not to Muscle.
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- Molecular Therapy, 2008, v. 16, n. 1, p. 30, doi. 10.1038/sj.mt.6300325
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- Publication type:
- Article
Brain natriuretic peptide is able to stimulate cardiac progenitor cell proliferation and differentiation in murine hearts after birth.
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- Basic Research in Cardiology, 2015, v. 110, n. 1, p. 1, doi. 10.1007/s00395-014-0455-4
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- Article
A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice.
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- DNA Research, 2004, v. 11, n. 6, p. 371, doi. 10.1093/dnares/11.6.371
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- Article
Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice.
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- PLoS Genetics, 2016, v. 12, n. 12, p. 1, doi. 10.1371/journal.pgen.1006510
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- Article