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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 6283419)

  • 81. An insertion of intracisternal A-particle retrotransposon in a novel member of the phosphoglycerate mutase family in the lew allele of mutant mice.
    Jiao Y; Jin X; Yan J; Jiao F; Li X; Roe BA; Jarrett HW; Gu W
    Genes Genet Syst; 2009 Oct; 84(5):327-34. PubMed ID: 20154419
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Metabolic regulation during early frog development. Identification of proteins labeled by 32P-glycolytic intermediates.
    Dworkin MB; Dworkin-Rastl E
    J Biol Chem; 1987 Dec; 262(35):17038-45. PubMed ID: 2824510
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Apparent change in reaction mechanism of phosphoglycerate mutase induced by salt.
    Grisolia S; Cascales M
    Biochem Biophys Res Commun; 1966 Jan; 22(2):200-5. PubMed ID: 5902293
    [No Abstract]   [Full Text] [Related]  

  • 84. Coexistence of diabetes and phosphofructokinase deficiency.
    Rubio SI; Naha KK; Sivakumar K; Dalakas MC; Poretsky L
    Endocr Pract; 1996; 2(2):100-2. PubMed ID: 15251550
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Whole-exome sequencing detects
    Thomas-Wilson A; Dharmadhikari AV; Heymann JJ; Jobanputra V; DiMauro S; Hirano M; Naini AB; Ganapathi M
    Cold Spring Harb Mol Case Stud; 2022 Feb; 8(2):. PubMed ID: 35022222
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Novel heterozygous mutations in the
    Sidhu M; Brady L; Vladutiu GD; Tarnopolsky MA
    Mol Genet Metab Rep; 2018 Dec; 17():53-55. PubMed ID: 30310767
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III mice.
    Pagliarani S; Lucchiari S; Ulzi G; Ripolone M; Violano R; Fortunato F; Bordoni A; Corti S; Moggio M; Bresolin N; Comi GP
    Biochim Biophys Acta Mol Basis Dis; 2018 Oct; 1864(10):3407-3417. PubMed ID: 30076962
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Glycolysis supports embryonic muscle growth by promoting myoblast fusion.
    Tixier V; Bataillé L; Etard C; Jagla T; Weger M; Daponte JP; Strähle U; Dickmeis T; Jagla K
    Proc Natl Acad Sci U S A; 2013 Nov; 110(47):18982-7. PubMed ID: 24191061
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Muscle glycogenoses: an overview.
    Di Mauro S
    Acta Myol; 2007 Jul; 26(1):35-41. PubMed ID: 17915567
    [No Abstract]   [Full Text] [Related]  

  • 90. The molecular genetic basis of muscle phosphoglycerate mutase (PGAM) deficiency.
    Tsujino S; Shanske S; Sakoda S; Fenichel G; DiMauro S
    Am J Hum Genet; 1993 Mar; 52(3):472-7. PubMed ID: 8447317
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency.
    Bresolin N; Comi GP; Fortunato F; Meola G; Gallanti A; Tajana A; Velicogna M; Gonano EF; Ninfali P; Pifferi S
    J Neurol; 1993 May; 240(5):272-7. PubMed ID: 8326330
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.
    Vita G; Toscano A; Bresolin N; Meola G; Fortunato F; Baradello A; Barbiroli B; Frassineti C; Zaniol P; Messina C
    J Neurol; 1994 Mar; 241(5):289-94. PubMed ID: 8006681
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility.
    Moroni I; Gonano EF; Comi GP; Tegazzin V; Prelle A; Bordoni A; Bresolin N; Scarlato G
    J Neurol; 1995 Feb; 242(3):127-33. PubMed ID: 7751854
    [TBL] [Abstract][Full Text] [Related]  

  • 94. [Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry].
    Deufel T; Paetzke I; Pongratz D; Hübner G; Wieland OH
    Klin Wochenschr; 1984 Jul; 62(14):651-8. PubMed ID: 6590924
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Muscle glucose-6-phosphate dehydrogenase deficiency.
    Bresolin N; Bet L; Moggio M; Meola G; Fortunato F; Comi G; Adobbati L; Geremia L; Pittalis S; Scarlato G
    J Neurol; 1989 May; 236(4):193-8. PubMed ID: 2760630
    [TBL] [Abstract][Full Text] [Related]  

  • 96. In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13.
    Castella-Escola J; Mattei MG; Ojcius DM; Passage E; Valentin C; Cohen-Solal M
    Hum Genet; 1990 Jan; 84(2):210-2. PubMed ID: 2153628
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency.
    Zimmer C; Altenkirch H; Dorfmüller-Küchlin S; Pongratz D; Paetzke I; Gosztonyi G
    J Neurol; 1991 Feb; 238(1):31-3. PubMed ID: 2030369
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Hereditary human myopathies in muscle culture.
    Meola G
    Ital J Neurol Sci; 1991 Jun; 12(3):257-68. PubMed ID: 1874604
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Muscle phosphoglycerate mutase deficiency.
    DiMauro S; Miranda AF; Olarte M; Friedman R; Hays AP
    Neurology; 1982 Jun; 32(6):584-91. PubMed ID: 6283419
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Human muscle phosphoglycerate mutase deficiency: newly discovered metabolic myopathy.
    DiMauro S; Miranda AF; Khan S; Gitlin K; Friedman R
    Science; 1981 Jun; 212(4500):1277-9. PubMed ID: 6262916
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.