These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
26. Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. Van Coster RN; Janssens S; Misson JP; Verloes A; Leroy JG Prenat Diagn; 1998 Oct; 18(10):1041-4. PubMed ID: 9826895 [TBL] [Abstract][Full Text] [Related]
27. Pyruvate Carboxylase Deficiency Type C: A Rare Cause of Acute Transient Flaccid Paralysis with Ketoacidosis. Almomen M; Sinclair G; Stockler-Ipsiroglu SG; Horvath GA Neuropediatrics; 2018 Dec; 49(6):369-372. PubMed ID: 30045381 [TBL] [Abstract][Full Text] [Related]
31. Novel Mutations in the PC Gene in Patients with Type B Pyruvate Carboxylase Deficiency. Ostergaard E; Duno M; Møller LB; Kalkanoglu-Sivri HS; Dursun A; Aliefendioglu D; Leth H; Dahl M; Christensen E; Wibrand F JIMD Rep; 2013; 9():1-5. PubMed ID: 23430542 [TBL] [Abstract][Full Text] [Related]
32. Clinical, biochemical, and molecular profiles of three Sri Lankan neonates with pyruvate carboxylase deficiency. Jasinge E; Fernando M; Indika NR; Ratnayake PD; Gamaathige N; Ratnaranjith R; Schroeder S; Jones P; Volha S; Jayasena S; Gunaratna AV; Bandara Ekanayake AN; Rolfs A Adv Lab Med; 2024 Jun; 5(2):205-212. PubMed ID: 38939194 [TBL] [Abstract][Full Text] [Related]
33. Evidence for two genetic complementation groups in pyruvate carboxylase-deficient human fibroblast cell lines. Feldman GL; Wolf B Biochem Genet; 1980 Jun; 18(5-6):617-24. PubMed ID: 6776949 [TBL] [Abstract][Full Text] [Related]
34. The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe. Robinson BH; Oei J; Saudubray JM; Marsac C; Bartlett K; Quan F; Gravel R Am J Hum Genet; 1987 Jan; 40(1):50-9. PubMed ID: 3101494 [TBL] [Abstract][Full Text] [Related]
35. Structural and promoter regions of the murine pyruvate carboxylase gene. Jitrapakdee S; Petchamphai N; Sunyakumthorn P; Wallace JC; Boonsaeng V Biochem Biophys Res Commun; 2001 Sep; 287(2):411-7. PubMed ID: 11554743 [TBL] [Abstract][Full Text] [Related]
36. Tao D; Zhang H; Yang J; Niu H; Zhang J; Zeng M; Cheng S Front Pediatr; 2022; 10():825515. PubMed ID: 35573952 [TBL] [Abstract][Full Text] [Related]
37. [Disorders of pyruvate metabolism and TCA cycle]. Kuroda Y Ryoikibetsu Shokogun Shirizu; 2001; (36):95-9. PubMed ID: 11596462 [No Abstract] [Full Text] [Related]
38. New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes. Moisan AM; Ricketts ML; Tardy V; Desrochers M; Mébarki F; Chaussain JL; Cabrol S; Raux-Demay MC; Forest MG; Sippell WG; Peter M; Morel Y; Simard J J Clin Endocrinol Metab; 1999 Dec; 84(12):4410-25. PubMed ID: 10599696 [TBL] [Abstract][Full Text] [Related]
39. Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Sagy M; Barzilay Z; Barash V; Oren M; Vardi P; Cohen BE; Gutman A Isr J Med Sci; 1981 Dec; 17(12):1159-63. PubMed ID: 6799424 [TBL] [Abstract][Full Text] [Related]
40. Hepatocyte nuclear factor 4α regulates the expression of the murine pyruvate carboxylase gene through the HNF4-specific binding motif in its proximal promoter. Chavalit T; Rojvirat P; Muangsawat S; Jitrapakdee S Biochim Biophys Acta; 2013 Oct; 1829(10):987-99. PubMed ID: 23665043 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]