Found: 21
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Skeletal Analysis of the Long Bone Abnormality ( lbab/ lbab) Mouse, A Novel Chondrodysplastic C-Type Natriuretic Peptide Mutant.
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- Calcified Tissue International, 2012, v. 90, n. 4, p. 307, doi. 10.1007/s00223-011-9567-0
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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
Role of Osteoclast Extracellular Signal-Regulated Kinase (ERK) in Cell Survival and Maintenance of Cell Polarity.
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- Journal of Bone & Mineral Research, 2003, v. 18, n. 7, p. 1198, doi. 10.1359/jbmr.2003.18.7.1198
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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
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
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
Expression of the Ellis-van Creveld ( Evc) gene in the rat tibial growth plate.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2004, v. 279A, n. 2, p. 729, doi. 10.1002/ar.a.20059
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- 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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- 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
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
Evidence for estrogen receptor expression in the bursal epithelial cells of chicks.
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- Animal Science Journal, 2005, v. 76, n. 3, p. 255, doi. 10.1111/j.1740-0929.2005.00264.x
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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
A nonsense mutation in mouse Adamtsl2 causes uterine hypoplasia and an irregular estrous cycle.
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- Mammalian Genome, 2023, v. 34, n. 4, p. 559, doi. 10.1007/s00335-023-10016-1
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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
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.
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- PLoS Genetics, 2015, v. 11, n. 8, p. 1, doi. 10.1371/journal.pgen.1005433
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- Article
Heparanase Localization during Palatogenesis in Mice.
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- BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/760236
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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