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Items: 1 to 20 of 113

1.

Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.

Barnard PJ, Derry JM, Ryder-Cook AS, Zander NF, Kilimann MW.

Cytogenet Cell Genet. 1990;53(2-3):91-4.

PMID:
1973380
2.

Mapping of a liver phosphorylase kinase alpha-subunit gene on the mouse X chromosome.

Geng Y, Derry JM, Hendrickx J, Coucke P, Willems PR, Barnard PJ.

Genomics. 1993 Jan;15(1):191-3.

PMID:
8432533
3.

Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13.

Francke U, Darras BT, Zander NF, Kilimann MW.

Am J Hum Genet. 1989 Aug;45(2):276-82.

4.

X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice.

Varsányi M, Vrbica A, Heilmeyer LM Jr.

Biochem Genet. 1980 Apr;18(3-4):247-61.

PMID:
7447922
5.
6.

Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22.

Willems PJ, Hendrickx J, Van der Auwera BJ, Vits L, Raeymaekers P, Coucke PJ, Van den Bergh I, Berger R, Smit GP, Van Broeckhoven C, et al.

Genomics. 1991 Apr;9(4):565-9.

PMID:
1674721
7.

The molecular basis of skeletal muscle phosphorylase kinase deficiency.

Cohen PT, Burchell A, Cohen P.

Eur J Biochem. 1976 Jul 1;66(2):347-56.

8.

Comparison of the physical and recombination maps of the mouse X chromosome.

Disteche CM, McConnell GK, Grant SG, Stephenson DA, Chapman VM, Gandy S, Adler DA.

Genomics. 1989 Aug;5(2):177-84.

PMID:
2571569
9.

Regional mapping of a liver alpha-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp.

Wauters JG, Bossuyt PJ, Davidson J, Hendrickx J, Kilimann MW, Willems PJ.

Cytogenet Cell Genet. 1992;60(3-4):194-6.

PMID:
1505214
10.
11.

Localisation of the gene encoding the catalytic gamma subunit of phosphorylase kinase to human chromosome bands 7p12-q21.

Jones TA, da Cruz e Silva EF, Spurr NK, Sheer D, Cohen PT.

Biochim Biophys Acta. 1990 Jan 30;1048(1):24-9.

PMID:
2297530
12.

Phosphorylase b kinase deficiency in man: a review.

Van den Berg IE, Berger R.

J Inherit Metab Dis. 1990;13(4):442-51. Review.

PMID:
2122111
13.

cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.

Davidson JJ, Ozçelik T, Hamacher C, Willems PJ, Francke U, Kilimann MW.

Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2096-100.

14.
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16.

Pyruvate dehydrogenase E1 alpha subunit genes in the mouse: mapping and comparison with human homologs.

Brown RM, Dahl HH, Brown GK.

Somat Cell Mol Genet. 1990 Sep;16(5):487-92.

PMID:
2122529
17.

Localization of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2).

Hendrickx J, Coucke P, Hors-Cayla MC, Smit GP, Shin YS, Deutsch J, Smeitink J, Berger R, Lee P, Fernandes J, et al.

Genomics. 1994 Jun;21(3):620-5.

PMID:
7959740
18.
19.

Phosphorylase kinase deficiency in I-strain mice is associated with a frameshift mutation in the alpha subunit muscle isoform.

Schneider A, Davidson JJ, Wüllrich A, Kilimann MW.

Nat Genet. 1993 Dec;5(4):381-5.

PMID:
8298647
20.

The gamma phosphorylase kinase gene, Phkg, maps to mouse chromosome 5 near Gus.

Maichele AJ, Chamberlain JS.

Mamm Genome. 1994 Jan;5(1):15-8.

PMID:
8111123
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