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Items: 1 to 20 of 36

1.
2.
3.

Gaucher disease: a century of delineation and understanding.

Desnick RJ.

Prog Clin Biol Res. 1982;95:1-30. Review. No abstract available.

PMID:
6750651
4.

A strategy to reveal high-frequency RFLPs along the human X chromosome.

Aldridge J, Kunkel L, Bruns G, Tantravahi U, Lalande M, Brewster T, Moreau E, Wilson M, Bromley W, Roderick T, et al.

Am J Hum Genet. 1984 May;36(3):546-64.

5.
6.

Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing.

Sanger F, Coulson AR, Barrell BG, Smith AJ, Roe BA.

J Mol Biol. 1980 Oct 25;143(2):161-78. No abstract available.

PMID:
6260957
8.

Human GM-CSF: molecular cloning of the complementary DNA and purification of the natural and recombinant proteins.

Wong GG, Witek JS, Temple PA, Wilkens KM, Leary AC, Luxenberg DP, Jones SS, Brown EL, Kay RM, Orr EC, et al.

Science. 1985 May 17;228(4701):810-5.

PMID:
3923623
9.

High-efficiency transformation of mammalian cells by plasmid DNA.

Chen C, Okayama H.

Mol Cell Biol. 1987 Aug;7(8):2745-52.

10.

An integrated family of amino acid sequence analysis programs.

Wolf H, Modrow S, Motz M, Jameson BA, Hermann G, Förtsch B.

Comput Appl Biosci. 1988 Mar;4(1):187-91.

PMID:
3382992
12.

alpha-N-acetylgalactosaminidase deficiency, a new lysosomal storage disorder.

van Diggelen OP, Schindler D, Willemsen R, Boer M, Kleijer WJ, Huijmans JG, Blom W, Galjaard H.

J Inherit Metab Dis. 1988;11(4):349-57.

PMID:
3149698
13.

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Saiki RK, Scharf S, Faloona F, Mullis KB, Horn GT, Erlich HA, Arnheim N.

Science. 1985 Dec 20;230(4732):1350-4.

PMID:
2999980
14.

Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease.

van Diggelen OP, Schindler D, Kleijer WJ, Huijmans JM, Galjaard H, Linden HU, Peter-Katalinic J, Egge H, Dabrowski U, Cantz M.

Lancet. 1987 Oct 3;2(8562):804. No abstract available.

PMID:
2889023
16.
17.

Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency.

Schindler D, Bishop DF, Wolfe DE, Wang AM, Egge H, Lemieux RU, Desnick RJ.

N Engl J Med. 1989 Jun 29;320(26):1735-40. No abstract available.

PMID:
2733734
18.

Enzymatic approaches for studying the structure, synthesis, and processing of glycoproteins.

Tarentino AL, Trimble RB, Plummer TH Jr.

Methods Cell Biol. 1989;32:111-39. Review. No abstract available.

PMID:
2691848
19.

Novel lysosomal glycoaminoacid storage disease with angiokeratoma corporis diffusum.

Kanzaki T, Yokota M, Mizuno N, Matsumoto Y, Hirabayashi Y.

Lancet. 1989 Apr 22;1(8643):875-7.

PMID:
2564952
20.

Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene.

Bernstein HS, Bishop DF, Astrin KH, Kornreich R, Eng CM, Sakuraba H, Desnick RJ.

J Clin Invest. 1989 Apr;83(4):1390-9.

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