Genetic lesions of bilirubin uridine‐diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler‐Najjar and Gilbert syndromes: correlation of genotype …
A Kadakol, SS Ghosh, BS Sappal, G Sharma… - Human …, 2000 - Wiley Online Library
Uridine‐diphosphoglucuronate glucuronosyltransferases (UGTs) are a family of enzymes
that conjugate various endogenous and exogenous compounds with glucuronic acid and …
that conjugate various endogenous and exogenous compounds with glucuronic acid and …
Reversal of hyperglycemia in mice by using human expandable insulin-producing cells differentiated from fetal liver progenitor cells
Beta-cell replacement is considered to be the most promising approach for treatment of type
1 diabetes. Its application on a large scale is hindered by a shortage of cells for …
1 diabetes. Its application on a large scale is hindered by a shortage of cells for …
Telomerase reconstitution immortalizes human fetal hepatocytes without disrupting their differentiation potential
Background & Aims: The availability of in vitro expandable human hepatocytes would
greatly advance liver-directed cell therapies. Therefore, we examined whether human fetal …
greatly advance liver-directed cell therapies. Therefore, we examined whether human fetal …
[HTML][HTML] Homodimerization of human bilirubin-uridine-diphosphoglucuronate glucuronosyltransferase-1 (UGT1A1) and its functional implications
SS Ghosh, BS Sappal, GV Kalpana, SW Lee… - Journal of Biological …, 2001 - ASBMB
Genetic lesions of bilirubin-uridine-diphosphoglucuronate glucuronosyltransferase-1
(UGT1A1) completely or partially abolish hepatic bilirubin glucuronidation, causing Crigler …
(UGT1A1) completely or partially abolish hepatic bilirubin glucuronidation, causing Crigler …
Amplification of engrafted hepatocytes by preparative manipulation of the host liver
C Guha, NJ Deb, BS Sappal, SS Ghosh… - Artificial …, 2001 - Wiley Online Library
Scarcity of donor livers is a major obstacle to the general application of hepatocytes for the
development of bioartificial liver assist devices as well as intracorporeal engraftment of …
development of bioartificial liver assist devices as well as intracorporeal engraftment of …
Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia …
A Kadakol, BS Sappal, SS Ghosh… - Journal of medical …, 2001 - jmg.bmj.com
E ditor—Crigler-Najjar syndrome types 1 and 2 (CN1 and CN2) are inherited as autosomal
recessive conditions and are characterised by severe non-haemolytic unconjugated …
recessive conditions and are characterised by severe non-haemolytic unconjugated …
A novel intronic mutation results in the use of a cryptic splice acceptor site within the coding region of UGT1A1, causing Crigler-Najjar syndrome type 1
BS Sappal, SS Ghosh, B Shneider, A Kadakol… - Molecular genetics and …, 2002 - Elsevier
Crigler-Najjar syndrome type 1 (CN-1) is characterized by severe unconjugated
hyperbilirubinemia due to an inherited deficiency of hepatic bilirubin …
hyperbilirubinemia due to an inherited deficiency of hepatic bilirubin …
Gene therapy for inherited hyperbilirubinemias
N Roy-Chowdhury, A Kadakol, BS Sappal… - Journal of …, 2001 - nature.com
Crigler-Najjar syndrome type 1 (CN-1) is a potentially lethal condition, and is the only
inherited disorder of bilirubin metabolism that needs treatment beyond the neonatal period …
inherited disorder of bilirubin metabolism that needs treatment beyond the neonatal period …
IMMORTALIZATION OF FETAL HUMAN LIVER CELLS WITH TELOMERASE RECONSTITUTION IS WITHOUT PERTURBATIONS IN CELL CYCLE CHECK-POINT …
BS Sappal, M Surana, V Kumaran, S Gupta - Hepatology, 2006 - journals.lww.com
Hepatocellular carcinoma (HCC) is one of the most common cancers in the world,
accounting for an estimated 600,000 deaths annually. Although much is known about both …
accounting for an estimated 600,000 deaths annually. Although much is known about both …
[CITATION][C] PROTEIN SYNTHESIS, POST-TRANSLATION MODIFICATION, AND DEGRADATION-Homodimerization of human bilirubin-uridine-diphos …
SS Ghosh, BS Sappal, GV Kalpana, SW Lee… - Journal of Biological …, 2001 - Baltimore [etc.]