[cite web | title = Entrez Gene: PHKB phosphorylase kinase, beta| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5257| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Brushia RJ, Walsh DA |title=Phosphorylase kinase: the complexity of its regulation is reflected in the complexity of its structure. |journal=Front. Biosci. |volume=4 |issue= |pages= D618–41 |year= 1999 |pmid= 10487978 |doi=
*cite journal | author=Daube H, Billich A, Mann K, Schramm HJ |title=Cleavage of phosphorylase kinase and calcium-free calmodulin by HIV-1 protease. |journal=Biochem. Biophys. Res. Commun. |volume=178 |issue= 3 |pages= 892–8 |year= 1991 |pmid= 1872871 |doi=
*cite journal | author=Francke U, Darras BT, Zander NF, Kilimann MW |title=Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13. |journal=Am. J. Hum. Genet. |volume=45 |issue= 2 |pages= 276–82 |year= 1989 |pmid= 2757032 |doi=
*cite journal | author=Wüllrich-Schmoll A, Kilimann MW |title=Structure of the human gene encoding the phosphorylase kinase beta subunit (PHKB). |journal=Eur. J. Biochem. |volume=238 |issue= 2 |pages= 374–80 |year= 1996 |pmid= 8681948 |doi=
*cite journal | author=Burwinkel B, Maichele AJ, Aagenaes O, "et al." |title=Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB). |journal=Hum. Mol. Genet. |volume=6 |issue= 7 |pages= 1109–15 |year= 1997 |pmid= 9215682 |doi=
*cite journal | author=van den Berg IE, van Beurden EA, de Klerk JB, "et al." |title=Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB). |journal=Am. J. Hum. Genet. |volume=61 |issue= 3 |pages= 539–46 |year= 1997 |pmid= 9326319 |doi=
*cite journal | author=Burwinkel B, Moses SW, Kilimann MW |title=Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the beta subunit gene (PHKB). |journal=Hum. Genet. |volume=101 |issue= 2 |pages= 170–4 |year= 1998 |pmid= 9402963 |doi=
*cite journal | author=Burwinkel B, Kilimann MW |title=Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease. |journal=J. Mol. Biol. |volume=277 |issue= 3 |pages= 513–7 |year= 1998 |pmid= 9533876 |doi= 10.1006/jmbi.1998.1641
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Burwinkel B, Hu B, Schroers A, "et al." |title=Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases. |journal=Eur. J. Hum. Genet. |volume=11 |issue= 7 |pages= 516–26 |year= 2004 |pmid= 12825073 |doi= 10.1038/sj.ejhg.5200996
*cite journal | author=Pallen MJ |title=Glucoamylase-like domains in the alpha- and beta-subunits of phosphorylase kinase. |journal=Protein Sci. |volume=12 |issue= 8 |pages= 1804–7 |year= 2004 |pmid= 12876330 |doi=
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Rual JF, Venkatesan K, Hao T, "et al." |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209
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