Pham-Dinh D - Search Results

1

Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene.

Pham-Dinh D, Boespflug-Tanguy O, Mimault C, Cavagna A, Giraud G, Leberre G, Lemarec B, Dautigny A. Pham-Dinh D, et al. Hum Mol Genet. 1993 Apr;2(4):465-7. doi: 10.1093/hmg/2.4.465. Hum Mol Genet. 1993. PMID: 7684945

2

Major Myelin proteolipid: the 4-alpha-helix topology.

Popot JL, Pham Dinh D, Dautigny A. Popot JL, et al. J Membr Biol. 1991 Mar;120(3):233-46. doi: 10.1007/BF01868534. J Membr Biol. 1991. PMID: 1711121

3

Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.

Pham-Dinh D, Popot JL, Boespflug-Tanguy O, Landrieu P, Deleuze JF, Boué J, Jollès P, Dautigny A. Pham-Dinh D, et al. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7562-6. doi: 10.1073/pnas.88.17.7562. Proc Natl Acad Sci U S A. 1991. PMID: 1715570 Free PMC article.

4

Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.

Boespflug-Tanguy O, Mimault C, Melki J, Cavagna A, Giraud G, Pham Dinh D, Dastugue B, Dautigny A. Boespflug-Tanguy O, et al. Am J Hum Genet. 1994 Sep;55(3):461-7. Am J Hum Genet. 1994. PMID: 7915877 Free PMC article.

5

Proteolipid DM-20 predominates over PLP in peripheral nervous system.

Pham-Dinh D, Birling MC, Roussel G, Dautigny A, Nussbaum JL. Pham-Dinh D, et al. Neuroreport. 1991 Feb;2(2):89-92. doi: 10.1097/00001756-199102000-00006. Neuroreport. 1991. PMID: 1715780

6

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome.

Mattei MG, Alliel PM, Dautigny A, Passage E, Pham-Dinh D, Mattei JF, Jollès P. Mattei MG, et al. Hum Genet. 1986 Apr;72(4):352-3. doi: 10.1007/BF00290964. Hum Genet. 1986. PMID: 3457761

7

The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23.

Pham-Dinh D, Fourbil Y, Blanquet F, Mattéi MG, Roeckel N, Latour P, Chazot G, Vandenberghe A, Dautigny A. Pham-Dinh D, et al. Hum Mol Genet. 1993 Dec;2(12):2051-4. doi: 10.1093/hmg/2.12.2051. Hum Mol Genet. 1993. PMID: 7509228

8

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.

Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C. Nelis E, et al. Hum Genet. 1994 Dec;94(6):653-7. doi: 10.1007/BF00206959. Hum Genet. 1994. PMID: 7527371

9

Structure and polymorphism of the mouse myelin/oligodendrocyte glycoprotein gene.

Daubas P, Pham-Dinh D, Dautigny A. Daubas P, et al. Genomics. 1994 Sep 1;23(1):36-41. doi: 10.1006/geno.1994.1456. Genomics. 1994. PMID: 7829100

10

Characterization and expression of the cDNA coding for the human myelin/oligodendrocyte glycoprotein.

Pham-Dinh D, Allinquant B, Ruberg M, Della Gaspera B, Nussbaum JL, Dautigny A. Pham-Dinh D, et al. J Neurochem. 1994 Dec;63(6):2353-6. doi: 10.1046/j.1471-4159.1994.63062353.x. J Neurochem. 1994. PMID: 7964757

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