CLPUB00600
Coriell L.L., Greene A.E., Mulivor R.A.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 6th edition. October 1979.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-168; National Institutes of Health; Bethesda; USA (1979) CLPUB00387
Coriell L.L., Greene A.E., Mulivor R.A.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 7th edition. October 1980.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda; USA (1980) PubMed=6280044; DOI=10.1002/mus.880050215
Pena S.D.J.
Giant axonal neuropathy: an inborn error of organization of intermediate filaments.
Muscle Nerve 5:166-172(1982) PubMed=6574472; DOI=10.1073/pnas.80.10.3086; PMCID=PMC393979
Kent C.M.
Increased rate of cell-substratum detachment of fibroblasts from patients with Duchenne muscular dystrophy.
Proc. Natl. Acad. Sci. U.S.A. 80:3086-3090(1983) PubMed=6667451
Taylor M.W., Kothari R.M., Holland G.D., Martinez-Valdez H., Zeige G.
A comparison of purine and pyrimidine pools in Bloom's syndrome and normal cells.
Cancer Biochem. Biophys. 7:19-25(1983) PubMed=6689020; DOI=10.1016/S0021-9258(17)43873-7
de Wet W.J., Chu M.-L., Prockop D.J.
The mRNAs for the pro-alpha 1(I) and pro-alpha 2(I) chains of type I procollagen are translated at the same rate in normal human fibroblasts and in fibroblasts from two variants of osteogenesis imperfecta with altered steady state ratios of the two mRNAs.
J. Biol. Chem. 258:14385-14389(1983) PubMed=6088703; DOI=10.1016/0022-510x(84)90174-6
Wright P.S., McKinney E., Berry S., Evers A., Kent C.M.
A functional membrane repair system in Duchenne muscular dystrophy fibroblasts.
J. Neurol. Sci. 64:259-264(1984) CLPUB00720
Greene A.E., Mulivor R.A.
1986/1987 catalog of cell lines. NIGMS human genetic mutant cell repository. 13th edition. October 1986.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda; USA (1986) PubMed=3745952; DOI=10.1111/1523-1747.ep12285424
Sephel G.C., Davidson J.M.
Elastin production in human skin fibroblast cultures and its decline with age.
J. Invest. Dermatol. 86:279-285(1986) PubMed=2445735; DOI=10.1016/S0021-9258(18)47730-7
Lin P.-Y., Gruenstein E.
Identification of a defective cAMP-stimulated Cl- channel in cystic fibrosis fibroblasts.
J. Biol. Chem. 262:15345-15347(1987) CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992) PubMed=8650226; DOI=10.1073/pnas.93.12.6101; PMCID=PMC39196
Zhao H.G., Li H.-H., Bach G., Schmidtchen A., Neufeld E.F.
The molecular basis of Sanfilippo syndrome type B.
Proc. Natl. Acad. Sci. U.S.A. 93:6101-6105(1996) PubMed=29125828; DOI=10.1242/dmm.030536; PMCID=PMC5719256
Napierala J.S., Li Y.-J., Lu Y., Lin K., Hauser L.A., Lynch D.R., Napierala M.
Comprehensive analysis of gene expression patterns in Friedreich's ataxia fibroblasts by RNA sequencing reveals altered levels of protein synthesis factors and solute carriers.
Dis. Model. Mech. 10:1353-1369(2017) | 
