MILTON FINEGOLD to Mutation
This is a "connection" page, showing publications MILTON FINEGOLD has written about Mutation.
Connection Strength
0.254
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Mutations in bile salt export pump (ABCB11) in two children with progressive familial intrahepatic cholestasis and cholangiocarcinoma. J Pediatr. 2007 May; 150(5):556-9.
Score: 0.074
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Characterization of pediatric hepatocellular carcinoma reveals genomic heterogeneity and diverse signaling pathway activation. Pediatr Blood Cancer. 2019 07; 66(7):e27745.
Score: 0.042
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Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis. Nat Commun. 2016 Feb 18; 7:10713.
Score: 0.034
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Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review. Hum Pathol. 2012 Jun; 43(6):943-51.
Score: 0.026
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Hepatoblastomas with carcinoma features represent a biological spectrum of aggressive neoplasms in children and young adults. J Hepatol. 2022 10; 77(4):1026-1037.
Score: 0.013
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Intrahepatic Cholestasis, Refractory Epilepsy, Skeletal Dysplasia, Endocrine Failure, and Dysmorphic Features in a Child With a Monoallelic 2q24-32.2 Deletion Encompassing ABCB11. Pediatr Dev Pathol. 2022 Mar-Apr; 25(2):174-179.
Score: 0.012
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NR1H4-related Progressive Familial Intrahepatic Cholestasis 5: Further Evidence for Rapidly Progressive Liver Failure. J Pediatr Gastroenterol Nutr. 2020 06; 70(6):e111-e113.
Score: 0.011
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Activating CAR and ?-catenin induces uncontrolled liver growth and tumorigenesis. Nat Commun. 2015 Feb 09; 6:5944.
Score: 0.008
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Mutations of PTCH1, MLL2, and MLL3 are not frequent events in hepatoblastoma. Pediatr Blood Cancer. 2012 Jun; 58(6):1006-7.
Score: 0.006
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Morphologic findings in progressive familial intrahepatic cholestasis 2 (PFIC2): correlation with genetic and immunohistochemical studies. Am J Surg Pathol. 2011 May; 35(5):687-96.
Score: 0.006
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Epigenetic changes play critical role in age-associated dysfunctions of the liver. Aging Cell. 2010 Oct; 9(5):895-910.
Score: 0.006
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Further evidence for EpCAM as the gene for congenital tufting enteropathy. Am J Med Genet A. 2010 Jan; 152A(1):222-4.
Score: 0.006
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Liver repopulation and correction of metabolic liver disease by transplanted adult mouse pancreatic cells. Am J Pathol. 2001 Feb; 158(2):571-9.
Score: 0.003
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Medical complications in long-term survivors with X-linked myotubular myopathy. J Pediatr. 1999 Feb; 134(2):206-14.
Score: 0.003
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p21(CIP1) and p57(KIP2) control muscle differentiation at the myogenin step. Genes Dev. 1999 Jan 15; 13(2):213-24.
Score: 0.003
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Alpha-1-antitrypsin deficiency: accumulation or degradation of mutant variants within the hepatic endoplasmic reticulum. Am J Respir Cell Mol Biol. 1989 Nov; 1(5):341-5.
Score: 0.001