Detalhe da pesquisa
1.
Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene.
Nat Genet
; 5(2): 130-4, 1993 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-8252038
2.
Hexokinase isoenzymes in human erythrocytes.
Science
; 159(3811): 215-6, 1968 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-4383736
3.
Second conserved domain of gp120 is important for HIV infectivity and antibody neutralization.
Science
; 239(4843): 1021-3, 1988 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-2830667
4.
HTLV-III in the semen and blood of a healthy homosexual man.
Science
; 226(4673): 451-3, 1984 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-6208608
5.
Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.
J Clin Invest
; 67(1): 149-55, 1981 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-7451647
6.
NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemia.
J Clin Invest
; 68(1): 279-85, 1981 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-6265499
7.
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.
J Clin Invest
; 88(4): 1161-6, 1991 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-1918370
8.
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.
J Clin Invest
; 92(2): 866-71, 1993 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-8349821
9.
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.
J Clin Invest
; 93(1): 99-105, 1994 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8282827
10.
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.
Brain
; 128(Pt 4): 732-42, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15689361
11.
Diaphorase P: a new fetal isozyme identified in human placenta.
Biochim Biophys Acta
; 613(1): 18-25, 1980.
Artigo
em Inglês
| MEDLINE | ID: mdl-6246954
12.
Soluble and microsomal forms of NADH-cytochrome beta 5 reductase from human placenta. Similarity with NADH-methemoglobin reductase from human erythrocytes.
Biochim Biophys Acta
; 481(1): 50-62, 1977 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-402944
13.
Soluble NADH-cytochrome b5 reductase from rabbit liver cytosol: partial purification and characterization.
Biochim Biophys Acta
; 526(1): 42-51, 1978 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28780
14.
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patients.
Eur J Hum Genet
; 4(3): 127-34, 1996.
Artigo
em Inglês
| MEDLINE | ID: mdl-8840112
15.
Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.
FEBS Lett
; 381(1-2): 15-20, 1996 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-8641426
16.
Detection of HIV-1 DNA in crude cell lysates of peripheral blood mononuclear cells by the polymerase chain reaction and nonradioactive oligonucleotide probes.
J Acquir Immune Defic Syndr (1988)
; 3(11): 1059-64, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2120419
17.
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation.
Neurology
; 54(5): 1075-9, 2000 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-10720277
18.
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.
Neurology
; 48(5): 1227-34, 1997 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-9153448
19.
3',5' Cyclic nucleotide phosphodiesterase from human platelets: effect of heat upon the multiple forms and their interconversion.
Biochimie
; 63(7): 603-9, 1981 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-6269658
20.
Expression of the transcripts initiated in the 62nd intron of the dystrophin gene.
Neuromuscul Disord
; 3(5-6): 519-24, 1993.
Artigo
em Inglês
| MEDLINE | ID: mdl-8186704