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Results: 1-25/28
Authors:
Holberg, CJ
Erickson, RP
Bernas, MJ
Witte, MH
Fultz, KE
Andrade, M
Witte, CL
Citation: Cj. Holberg et al., Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families, AM J MED G, 98(4), 2001, pp. 303-312
Authors:
Baruch, AC
Erickson, RP
Citation: Ac. Baruch et Rp. Erickson, Axenfeld-Rieger anomaly, hypertelorism, clinodactyly, and cardiac anomalies in sibs with an unbalanced translocation der(6)t(6;8), AM J MED G, 100(3), 2001, pp. 187-190
Authors:
Holberg, CJ
Halonen, M
Solomon, S
Graves, PE
Baldini, M
Erickson, RP
Martinez, FD
Citation: Cj. Holberg et al., Factor analysis of asthma and atopy traits shows 2 major components, one of which is linked to markers on chromosome 5q, J ALLERG CL, 108(5), 2001, pp. 772-780
Authors:
Erickson, RP
Graves, PE
Citation: Rp. Erickson et Pe. Graves, Genetic variation in beta-adrenergic receptors and their relationship to susceptibility for asthma and therapeutic response, DRUG META D, 29(4), 2001, pp. 557-561
Authors:
Erickson, RP
Citation: Rp. Erickson, Lymphedema-distichiasis and FOXC2 gene mutations, LYMPHOLOGY, 34(1), 2001, pp. 1-1
Authors:
Camargo, F
Erickson, RP
Garver, WS
Hossain, GS
Carbone, PN
Heidenreich, RA
Blanchard, J
Citation: F. Camargo et al., Cyclodextrins in the treatment of a mouse model of Niemann-Pick C disease, LIFE SCI, 70(2), 2001, pp. 131-142
Authors:
Erickson, RP
Dagenais, SL
Caulder, MS
Downs, CA
Herman, G
Jones, MC
Kerstjens-Frederikse, WS
Lidral, AC
McDonald, M
Nelson, CC
Witte, M
Glover, TW
Citation: Rp. Erickson et al., Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations, J MED GENET, 38(11), 2001, pp. 761-766
Authors:
Erickson, RP
Kiela, M
Garver, WS
Krishnan, K
Heidenreich, RA
Citation: Rp. Erickson et al., Cholesterol signaling at the endoplasmic reticulum occurs in npc1(-/-) butnot in npc1(-/-), LDLR-/- mice, BIOC BIOP R, 284(2), 2001, pp. 326-330
Authors:
Hsu, SJ
Erickson, RP
Zhang, JS
Garver, WS
Heidenreich, RA
Citation: Sj. Hsu et al., Fine linkage and physical mapping suggests cross-over suppression with a retroposon insertion at the npc1 mutation, MAMM GENOME, 11(9), 2000, pp. 774-778
Authors:
Zhang, JS
Erickson, RP
Citation: Js. Zhang et Rp. Erickson, A modifier of Niemann-Pick C 1 maps to mouse chromosome 19, MAMM GENOME, 11(1), 2000, pp. 69-71
Authors:
Hsu, SC
Erickson, RP
Citation: Sc. Hsu et Rp. Erickson, Construction of a long-range YAC physical map spanning the 10-cM region between the markers D18Mit109 and D18Mit68 on mouse proximal chromosome 18, GENOME, 43(3), 2000, pp. 427-433
Authors:
Pujol, LA
Erickson, RP
Heidenreich, RA
Cunniff, C
Citation: La. Pujol et al., Variable presentation of Rothmund-Thomson syndrome, AM J MED G, 95(3), 2000, pp. 204-207
Authors:
Erickson, RP
Garver, WS
Camargo, F
Hossian, GS
Heidenreich, RA
Citation: Rp. Erickson et al., Pharmacological and genetic modifications of somatic cholesterol do not substantially alter the course of CNS disease in Niemann-Pick C mice, J INH MET D, 23(1), 2000, pp. 54-62
Authors:
Graves, PE
Kabesch, M
Halonen, M
Holberg, CJ
Baldini, M
Fritzsch, C
Weiland, SK
Erickson, RP
von Mutius, E
Martinez, FD
Citation: Pe. Graves et al., A cluster of seven tightly linked polymorphisms in the IL-13 gene is associated with total serum IgE levels in three populations of white children, J ALLERG CL, 105(3), 2000, pp. 506-513
Authors:
Erickson, RP
Citation: Rp. Erickson, The evolution of neural coding ideas in the chemical senses, PHYSL BEHAV, 69(1-2), 2000, pp. 3-13
Authors:
Ganchrow, D
Erickson, RP
Citation: D. Ganchrow et Rp. Erickson, Taste quality and intensity: Lessons from the Morrison technique, PHYSL BEHAV, 69(1-2), 2000, pp. 121-133
Authors:
Liu, L
Welch, JM
Erickson, RP
Reinhart, PH
Simon, SA
Citation: L. Liu et al., Different responses to repeated applications of zingerone in behavioral studies, recordings from intact and cultured TG neurons, and from VR1 receptors, PHYSL BEHAV, 69(1-2), 2000, pp. 177-186
Authors:
Garver, WS
Heidenreich, RA
Erickson, RP
Thomas, MA
Wilson, JM
Citation: Ws. Garver et al., Localization of the murine Niemann-Pick C1 protein to two distinct intracellular compartments, J LIPID RES, 41(5), 2000, pp. 673-687
Authors:
Fang, JM
Dagenais, SL
Erickson, RP
Arlt, MF
Glynn, MW
Gorski, JL
Seaver, LH
Glover, TW
Citation: Jm. Fang et al., Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome, AM J HU GEN, 67(6), 2000, pp. 1382-1388
Authors:
Erickson, RP
Citation: Rp. Erickson, Southwestern Athabaskan (Navajo and Apache) genetic diseases, GENET MED, 1(4), 1999, pp. 151-157
Authors:
Erickson, RP
Citation: Rp. Erickson, Use of antisense to study gene expression, METHODS, 18(3), 1999, pp. 241-243
Authors:
Erickson, RP
Citation: Rp. Erickson, Antisense transgenics in animals, METHODS, 18(3), 1999, pp. 304-310
Authors:
Baldini, M
Lohman, IC
Halonen, M
Erickson, RP
Holt, PG
Martinez, FD
Citation: M. Baldini et al., A polymorphism in the 5 ' flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E, AM J RESP C, 20(5), 1999, pp. 976-983
Authors:
Aleck, KA
Argueso, L
Stone, J
Hackel, JG
Erickson, RP
Citation: Ka. Aleck et al., True hermaphroditism with partial duplication of chromosome 22 and withoutSRY, AM J MED G, 85(1), 1999, pp. 2-4
Authors:
Graves, PE
Davis, D
Erickson, RP
Lopez, M
Kofman-Alfaro, S
Mendez, JP
Speer, IE
Citation: Pe. Graves et al., Ascertainment and mutational studies of SRY in nine XY females, AM J MED G, 83(2), 1999, pp. 138-139