Any link on the below references will take you off
of the BMCB site and to an abstract of that particular paper.
Ahmad, I., S. Lope-Piedrafita, X. Bi, C. Hicks, Y. Yao, C. Yu, E.
Chaitkin, C.M. Howison, L. Weberg, T.P. Trouard, and R.P. Erickson
RP. 2005. Allopregnanolone treatment, both as a single injection
or repetitively, delays demyelination and enhances survival of Niemann-Pick
C mice. Journal of Neuroscience Research 82: 811-821.
Trouard, T.P., R.A. Heidenreich, J.F. Seeger, and R.P. Erickson.
2005. Diffusion tensor imaging in Niemann-Pick Type C disease. Pediatric
Neurology 33: 325-330.
Cao, W., B. Chau, R. Hunter, D. Strnatka, C.A. McQueen, and R.P.
Erickson. 2005. Only low levels of exogenous N-acetyltransferase
can be achieved in transgenic mice. Pharmacogenomics
Journal 5: 255-261.
Cao, W., R. Hunter, D. Strnatka, C.A. McQueen, and R.P. Erickson
RP. 2005. DNA constructs designed to produce short hairpin, interfering
RNAs in transgenic mice sometimes show early lethality and an interferon
response. Journal
of Applied Genetics 46: 217-225.
Erickson, R.P., I.J. Karolyi, and S.R. Diehl SR. 2005. Correlation
of susceptibility to 6-aminonicotinamide and hydrocortisone-induced
cleft palate. Life
Sciences 76: 2071-2078.
Erickson, R.P., A. Bhattacharyya, R.J. Hunter, and R.A. Heidenreich,
and N.J. Cherrington. 2005. Liver disease with altered bile acid
transport in Niemann-Pick C mice on a high-fat, 1% cholesterol diet. American Journal of Physiology Gastrointestinal and Liver Physiology 289: G300-G307.
Erickson, R.P. 2005. Agenesis of tibia with bifid femur, congenital
heart disease, and cleft lip with cleft palate or tracheoesophageal
fistula: possible variants of Gollop-Wolfgang complex. American
Journal of Medical Genetics, Part A 134: 315-317.
Bascunan-Castillo, E.C., R.P. Erickson, C.M. Howison, R.J. Hunter,
R.H. Heidenreich, C. Hicks, T.P. Trouard, and R.J. Gillies. 2004.
Tamoxifen and vitamin E treatments delay symptoms in the mouse model
of Niemann-Pick C. Journal
of Applied Genetics 45: 461-467.
Erickson, R.P., S. Skinner, H. Jacquet, D. Campion, P.G. Buckley,
K.K. Mantripragada, and J.P. Dumanski. 2003. Does chromosome 22
have anything to do with sex determination: further studies on a
46,XX,22q11.2 del male. American
Journal of Medical Genetics, Part A 123: 64-67.
Wang, L.L., A. Gannavarapu, C.L. Clericuzio, R.P. Erickson, A.D.
Irvine, and S.E. Plon. 2003. Absence of RECQL4 mutations in poikiloderma
with neutropenia in Navajo and non-Navajo patients. American
Journal of Medical Genetics 118A: 299-301.
Vincent, I., B. Bu, and R.P. Erickson. 2003. Understanding Niemann-Pick
type C disease: a fat problem. Current
Opinion in Neurology 16: 155-161.
Erickson, R.P. 2003. Somatic gene mutation and human disease other
than cancer. Mutation
Research 543: 125-136.
Nonn, L., R.R. Williams, R.P. Erickson, and G. Powis. 2003. The
absence of mitochondrial thioredoxin 2 causes massive apoptosis,
exencephaly, and early embryonic lethality in homozygous mice. Molecular
and Cellular Biology 23: 916-922.
Yi, Z., N. Garrison, O. Cohen-Barak, T.M. Karafet, R.A. King, R.P.
Erickson, M.F. Hammer, and M.H. Brilliant. 2003. A 122.5-kilobase
deletion of the P gene underlies the high prevalence of oculocutaneous
albinism type 2 in the Navajo population. American
Journal of Human Genetics 72: 62-72.
Loftus, S.K., R.P. Erickson, S.U. Walkley, M.A. Bryant, A. Incao,
R.A. Heidenreich, and W.J. Pavan. 2002. Rescue of neurodegeneration
in Niemann-Pick C mice by a prion-promoter-driven Npc1 cDNA transgene. Human
Molecular Genetics 11:3107-3114.
Erickson, R.P., and O. Bernard. 2002. Studies on neuronal death
in the mouse model of Niemann-Pick C disease. Journal
of Neuroscience Research 68: 738-744.
Erickson, R.P., M. Kiela, P.J. Devine, P.B. Hoyer, and R.A. Heidenreich.
2002. mdr1a deficiency corrects sterility in Niemann-Pick C1 protein
deficient female mice. Molecular
Reproduction and Development 62: 167-173.
Erickson, R.P. 2001. Forkhead genes and human disease. Journal
of Applied Genetics 42: 211-221.
Camargo, F., R.P. Erickson, W.S. Garver, G.S. Hossain, P.N. Carbone,
R.A. Heidenreich, and J. Blanchard. 2001. Cyclodextrins in the treatment
of a mouse model of Niemann-Pick C disease. Life
Sciences 70: 131-142.
Erickson, R.P., S.L. Dageneis, M.S. Caulder, C.A. Downs, G. Herman,
M.D. Jones, W.S. Kerstjens-Frederikse, A.C. Lidral, M. McDonald,
C.C. Nelson, M. Witte, and T.W. Glover. 2001. Clinical heterogeneity
in lymphedema-distichiasis with FOXC2 truncating mutations. Journal
of Medical Genetics 38: 761-766.
Fang, J., S.L. Dagenais, R.P. Erickson, M.F. Arlt, M.W. Glynn,
J.L. Gorski, L.H. Seaver, and T.W. Glover. 2000. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are
responsible for the hereditary lymphedema-distichiasis syndrome. American
Journal of Human Genetics 67: 1382-1388.
Hsu, S.J., R.P. Erickson, J. Zhang, W.S. Garver, and R.A. Heidenreich.
2000. Fine linkage and physical mapping suggests cross-over suppression
with a retroposon insertion at the npc1 mutation. Mammalian
Genome 11: 774-778.
Zhang, J., and R.P. Erickson. 2000. A modifier of Niemann Pick
C 1 maps to mouse chromosome 19. Mammalian
Genome 11: 69-71.
