Grochowski, Christopher M; Loomes, Kathleen M; Spinner, Nancy B (2016) Jagged1 (JAG1): Structure, expression, and disease associations. Gene 576:381-4 |
Kamath, Binita M; Podkameni, Gisele; Hutchinson, Anne L et al. (2012) Renal anomalies in Alagille syndrome: a disease-defining feature. Am J Med Genet A 158A:85-9 |
Penton, Andrea L; Leonard, Laura D; Spinner, Nancy B (2012) Notch signaling in human development and disease. Semin Cell Dev Biol 23:450-7 |
Kamath, Binita M; Munoz, Pedro S; Bab, Natalie et al. (2010) A longitudinal study to identify laboratory predictors of liver disease outcome in Alagille syndrome. J Pediatr Gastroenterol Nutr 50:526-30 |
Bauer, Robert C; Laney, Ayanna O; Smith, Rosemarie et al. (2010) Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis. Hum Mutat 31:594-601 |
Bales, Christina B; Kamath, Binita M; Munoz, Pedro S et al. (2010) Pathologic lower extremity fractures in children with Alagille syndrome. J Pediatr Gastroenterol Nutr 51:66-70 |
Leyva-Vega, Melissa; Gerfen, Jennifer; Thiel, Brian D et al. (2010) Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3. Am J Med Genet A 152A:886-95 |
Kamath, Binita M; Thiel, Brian D; Gai, Xiaowu et al. (2009) SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation. Hum Mutat 30:371-8 |
Ryan, Matthew J; Bales, Christina; Nelson, Anthony et al. (2008) Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype. Hepatology 48:1989-97 |
Warthen, D M; Moore, E C; Kamath, B M et al. (2006) Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate. Hum Mutat 27:436-43 |
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