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Results:
1-7
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Results: 7
Authors:
Mardh, CK
Backman, B
Simmons, D
Golovleva, I
Gu, TT
Holmgren, G
MacDougall, M
Forsman-Semb, K
Citation: Ck. Mardh et al., Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients, EUR J OR SC, 109(1), 2001, pp. 8-13
Authors:
Hu, JCC
Zhang, CH
Yang, Y
Karrman-Mardh, C
Forsman-Semb, K
Simmer, JP
Citation: Jcc. Hu et al., Cloning and characterization of the mouse and human enamelin genes, J DENT RES, 80(3), 2001, pp. 898-902
Authors:
Burstedt, MSL
Forsman-Semb, K
Golovleva, I
Janunger, T
Wachtmeister, L
Sandgren, O
Citation: Msl. Burstedt et al., Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene, ARCH OPHTH, 119(2), 2001, pp. 260-267
Authors:
MacDougall, M
Simmons, D
Gu, TT
Forsman-Semb, K
Mardh, CK
Mesbah, M
Forest, N
Krebsbach, PH
Yamada, Y
Berdal, A
Citation: M. Macdougall et al., Cloning, characterization and immunolocalization of human ameloblastin, EUR J OR SC, 108(4), 2000, pp. 303-310
Authors:
Xia, Y
Gally, D
Forsman-Semb, K
Uhlin, BE
Citation: Y. Xia et al., Regulatory cross-talk between adhesin operons in Escherichia coli: inhibition of type 1 fimbriae expression by the PapB protein, EMBO J, 19(7), 2000, pp. 1450-1457
Authors:
Burstedt, MSI
Sandgren, O
Holmgren, G
Forsman-Semb, K
Citation: Msi. Burstedt et al., Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26, INV OPHTH V, 40(5), 1999, pp. 995-1000
Authors:
Stathakis, DG
Udar, N
Sandgren, O
Andreasson, S
Bryant, PJ
Small, K
Forsman-Semb, K
Citation: Dg. Stathakis et al., Genomic organization of human DLG4, the gene encoding postsynaptic density95, J NEUROCHEM, 73(6), 1999, pp. 2250-2265
Risultati:
1-7
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