Pages that link to "Q36468498"

The following pages link to Isolation and sequence analysis of a cDNA clone encoding the entire catalytic subunit of phosphorylase kinase (Q36468498):

Displaying 22 items.

• The substrate specificity and structure of mitogen-activated protein (MAP) kinase-activated protein kinase-2 (Q24528645) (← links)
• Molecular genetics of phosphorylase kinase: cDNA cloning, chromosomal mapping and isoform structure (Q28302930) (← links)
• cDNA cloning and complete primary structure of skeletal muscle phosphorylase kinase (alpha subunit) (Q33569294) (← links)
• Structure of the human gene encoding the phosphorylase kinase beta subunit (PHKB). (Q34386827) (← links)
• 1 Protein kinase classification (Q34763605) (← links)
• Molecular cloning and chromosomal localization of a novel Drosophila protein phosphatase. (Q35437676) (← links)
• Use of DNA sequence and mutant analyses and antisense oligodeoxynucleotides to examine the molecular basis of nonmuscle myosin light chain kinase autoinhibition, calmodulin recognition, and activity (Q36223815) (← links)
• Isolation and sequence analysis of a cDNA clone encoding a type-1 protein phosphatase catalytic subunit: homology with protein phosphatase 2A. (Q36287193) (← links)
• A second catalytic subunit of type-2A protein phosphatase from rabbit skeletal muscle (Q36297896) (← links)
• Identification of a novel protein phosphatase catalytic subunit by cDNA cloning (Q36369647) (← links)
• Isolation and sequence analysis of a cDNA clone encoding the entire catalytic subunit of a type-2A protein phosphatase (Q36427347) (← links)
• Nucleotide sequence of cDNA encoding the catalytic subunit of phosphorylase kinase from rat soleus muscle (Q40553585) (← links)
• DPhK-gamma, a putative Drosophila kinase with homology to vertebrate phosphorylase kinase gamma subunits: molecular characterisation of the gene and phenotypic analysis of loss of function mutants (Q42687372) (← links)
• Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22 (Q44114798) (← links)
• Autosomal Recessive Liver Phosphorylase Kinase Deficiency Caused by a Novel Splice-Site Mutation in the Gene Encoding the Liver Gamma Subunit (PHKG2) (Q44214371) (← links)
• Complete coding sequences of cDNAs of four variants of rabbit skeletal muscle troponin T (Q44679189) (← links)
• Hepatic phosphorylase b kinase deficiency with normal enzyme activity in leukocytes (Q46555197) (← links)
• RPK1, an essential yeast protein kinase involved in the regulation of the onset of mitosis, shows homology to mammalian dual-specificity kinases (Q48081745) (← links)
• The association of phosphorylase kinase with membranes of rat liver smooth endoplasmic reticulum (Q51583141) (← links)
• E. coli expression and characterization of a mutant troponin I with the three cysteine residues substituted. (Q54657194) (← links)
• Myopathic evolution of an exertional muscle pain syndrome with phosphorylase b kinase deficiency (Q68381278) (← links)
• The testis isoform of the phosphorylase kinase catalytic subunit (PhK-gammaT) plays a critical role in regulation of glycogen mobilization in developing lung (Q71142810) (← links)