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Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 7, 2002
Confirmation and high resolution mapping of an atherosclerosis susceptibility gene in mice on Chromosome 1Shelley A Phelan, David R Beier, David C Higgins, et al.Plant Physiology|March 1, 1980
Some synthetic phytotoxins structurally related to rhynchosporosideJ P Beltran, G A Strobel, R Beier, et al.Genomics|February 18, 1998
The mouse chondroadherin gene: characterization and chromosomal localizationC Landgren, D R Beier, R Fässler, et al.The Journal of Urology|January 1, 1994
The in vitro cytotoxicity of urine from patients with interstitial cystitisR Beier-Holgersen, G G Hermann, S O Mortensen, et al.Genomics|June 15, 1997
LTW4 protein on mouse chromosome 1 is a member of a family of antioxidant proteinsO A Iakoubova, L A Pacella, H Her, et al.Journal of Cell Science|June 24, 2025
Inhibition of Hedgehog signaling does not mitigate polycystic kidney disease severity in a Pkd1 mutant mouse modelSean K Gombart, Scott Houghtaling, Tzu-Hua Ho, et al.The Journal of Biological Chemistry|November 5, 1997
The matrix metalloproteinase-14 (MMP-14) gene is structurally distinct from other MMP genes and is co-expressed with the TIMP-2 gene during mouse embryogenesisS S Apte, N Fukai, D R Beier, et al.Matrix Biology : Journal of the International Society for Matrix Biology|May 6, 1998
Sequence, structure and chromosomal localization of Crtm gene encoding mouse cartilage matrix protein and its exclusion as a candidate for murine achondroplasiaA Aszódi, D R Beier, L Hiripi, et al.Cerebral Cortex (New York, N.Y. : 1991)|August 24, 2013
A forward genetic screen in mice identifies mutants with abnormal cortical patterningSeungshin Ha, Rolf W Stottmann, Andrew J Furley, et al.G3 (Bethesda, Md.)|June 5, 2016
Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in MiceSeungshin Ha, Anna M Lindsay, Andrew E Timms, et al.Pageof 25