Connection

MILTON FINEGOLD to Mutation

This is a "connection" page, showing publications MILTON FINEGOLD has written about Mutation.
Connection Strength

0.254
  1. 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.
    View in: PubMed
    Score: 0.074
  2. Characterization of pediatric hepatocellular carcinoma reveals genomic heterogeneity and diverse signaling pathway activation. Pediatr Blood Cancer. 2019 07; 66(7):e27745.
    View in: PubMed
    Score: 0.042
  3. Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis. Nat Commun. 2016 Feb 18; 7:10713.
    View in: PubMed
    Score: 0.034
  4. 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.
    View in: PubMed
    Score: 0.026
  5. Hepatoblastomas with carcinoma features represent a biological spectrum of aggressive neoplasms in children and young adults. J Hepatol. 2022 10; 77(4):1026-1037.
    View in: PubMed
    Score: 0.013
  6. 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.
    View in: PubMed
    Score: 0.012
  7. NR1H4-related Progressive Familial Intrahepatic Cholestasis 5: Further Evidence for Rapidly Progressive Liver Failure. J Pediatr Gastroenterol Nutr. 2020 06; 70(6):e111-e113.
    View in: PubMed
    Score: 0.011
  8. Activating CAR and ?-catenin induces uncontrolled liver growth and tumorigenesis. Nat Commun. 2015 Feb 09; 6:5944.
    View in: PubMed
    Score: 0.008
  9. Mutations of PTCH1, MLL2, and MLL3 are not frequent events in hepatoblastoma. Pediatr Blood Cancer. 2012 Jun; 58(6):1006-7.
    View in: PubMed
    Score: 0.006
  10. 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.
    View in: PubMed
    Score: 0.006
  11. Epigenetic changes play critical role in age-associated dysfunctions of the liver. Aging Cell. 2010 Oct; 9(5):895-910.
    View in: PubMed
    Score: 0.006
  12. Further evidence for EpCAM as the gene for congenital tufting enteropathy. Am J Med Genet A. 2010 Jan; 152A(1):222-4.
    View in: PubMed
    Score: 0.006
  13. Liver repopulation and correction of metabolic liver disease by transplanted adult mouse pancreatic cells. Am J Pathol. 2001 Feb; 158(2):571-9.
    View in: PubMed
    Score: 0.003
  14. Medical complications in long-term survivors with X-linked myotubular myopathy. J Pediatr. 1999 Feb; 134(2):206-14.
    View in: PubMed
    Score: 0.003
  15. p21(CIP1) and p57(KIP2) control muscle differentiation at the myogenin step. Genes Dev. 1999 Jan 15; 13(2):213-24.
    View in: PubMed
    Score: 0.003
  16. 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.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.