Molecular Genetics and Metabolism

Histone acetylation and chromatin remodeling: which comes first?
pp. 1-5(5)
Authors: Neely K.E.; Workman J.L.

Mechanisms for storage of prolactin and growth hormone in secretory granules
pp. 6-13(8)
Author: Dannies P.S.

Mutation screening and association of human retinoid X receptor variation with lipid levels in familial type 2 diabetes
pp. 14-22(9)
Authors: Wang H.; Chu W.; Hemphill C.; Hasstedt S.J.; Elbein S.C.

Fabry disease: 45 novel mutations in the -galactosidase A gene causing the classical phenotype
pp. 23-30(8)
Authors: Shabbeer J.; Yasuda M.; Luca E.; Desnick R.J.

The Niemann–Pick C1 protein in feline fibroblasts
pp. 31-36(6)
Authors: Garver W.S.; Somers K.; Krishnan K.; Mitchell T.; Heidenreich R.A.; Anna Thrall M.

Cloning and characterization of glucose transporter 11, a novel sugar transporter that is alternatively spliced in various tissues
pp. 37-45(9)
Authors: Wu X.; Li W.; Sharma V.; Godzik A.; Freeze H.H.

1,25-Dihydroxy-3-epi-vitamin D₃, a natural metabolite of 1,25-dihydroxy vitamin D₃: production and biological activity studies in pulmonary alveolar type II cells
pp. 46-56(11)
Authors: Rehan V.K.; Torday J.S.; Peleg S.; Gennaro L.; Vouros P.; Padbury J.; Sunita Rao D.; Satyanarayana Reddy G.

Novel mutations in the PATCHED gene in basal cell nevus syndrome
pp. 57-61(5)
Authors: Lam C-W.; Leung C-Y.; Lee K-C.; Xie J.; Lo F-M.; Au T-S.; Tong S-F.; Poon M-K.; Chan L-Y.; Luk N-M.

Molecular characterization of 21 X-ALD Portuguese families: identification of eight novel mutations in the ABCD1 gene
pp. 62-67(6)
Authors: Guimaraes C.P.; Lemos M.; Sa´-Miranda C.; Azevedo J.E.

Ornithine transcarbamylase deficiency: a novel splice site mutation in a family with meiotic recombination and a new useful SNP for diagnosis
pp. 68-70(3)
Authors: Azevedo L.; Vilarinho L.; Leao Teles E.; Amorim A.

Remark on utility and error rates of the allopurinol test in detecting mild ornithine transcarbamylase deficiency
pp. 71-75(5)
Authors: Oexle K.; Bonafe´ L.; Steinmann B.

A heterozygote phenotype is present in the jvs +/- mutant mouse livers
pp. 76-80(5)
Authors: Lahjouji K.; Elimrani I.; Wu J.; Mitchell G.A.; Qureshi I.A.

Hypocarnitinemia in lysinuric protein intolerance
pp. 81-83(3)
Authors: Korman S.H.; Raas-Rothschild A.; Elpeleg O.; Gutman A.