Treatment of human immunodeficiency virus infections.

Por Hirsch, M S, Kaplan, J C
Publicado em 1987

Pathogenesis of human immunodeficiency virus infection and prospects for control.

Por Ho, D. D., Kaplan, J. C.
Publicado em 1987

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 cong...

Por Lostanlen, D, Lenoir, G, Kaplan, J C
Publicado em 1981

Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.

Por Choury, D, Leroux, A, Kaplan, J C
Publicado em 1981

Male infertility as the only presenting sign of cystic fibrosis when homozygous for the mild mutation R117H.

Por Bienvenu, T, Beldjord, C, Adjiman, M, Kaplan, J C
Publicado em 1993

Interaction between cytochrome b5 and hemoglobin: involvement of beta 66 (E10) and beta 95 (FG2) lysyl residues of hemoglobin.

Por Gacon, G, Lostanlen, D, Labie, D, Kaplan, J C
Publicado em 1980

Alpha interferon and acyclovir treatment of herpes simplex virus in lymphoid cell cultures.

Por Hammer, S M, Kaplan, J C, Lowe, B R, Hirsch, M S
Publicado em 1982

Illegitimate transcription: transcription of any gene in any cell type.

Por Chelly, J, Concordet, J P, Kaplan, J C, Kahn, A
Publicado em 1989

Excision of viral DNA from host cell DNA after induction of simian virus 40-transformed hamster cells.

Por Rakusanova, T, Kaplan, J C, Smales, W P, Black, P H
Publicado em 1976

Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene.

Por Bienvenu, T, Beldjord, C, Fonknechten, N, Kaplan, J C, Lenoir, G
Publicado em 1993

Severe cystic fibrosis phenotype in a delta F508/3272-26A-->G compound heterozygote.

Por Bienvenu, T, Beldjord, C, Kaplan, J C, Hubert, D, Dusser, D
Publicado em 1995

Susceptibility testing by polymerase chain reaction DNA quantitation: a method to measure drug resistance of human immunodeficiency virus type 1 isolates.

Por Eron, J J, Gorczyca, P, Kaplan, J C, D'Aquila, R T
Publicado em 1992

A T to G mutation in the polypyrimidine tract of the second intron of the human beta-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interaction...

Por Sébillon, P, Beldjord, C, Kaplan, J C, Brody, E, Marie, J
Publicado em 1995

A new TaqI allele at DXS52 frequent in Algeria.

Por Nafa, K, Reghis, A, Benabadji, M, Delpech, M, Kaplan, J C
Publicado em 1989

A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD)

Por Hugnot, J.P., Récan, D., Jeanpierre, M., Kaplan, J.C., Tolun, A.
Publicado em 1991

Human chromosome 22.

Por Kaplan, J C, Aurias, A, Julier, C, Prieur, M, Szajnert, M F
Publicado em 1987

Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.

Por Haliassos, A, Chomel, J C, Grandjouan, S, Kruh, J, Kaplan, J C, Kitzis, A
Publicado em 1989

Effects of zidovudine-selected human immunodeficiency virus type 1 reverse transcriptase amino acid substitutions on processive DNA synthesis and viral replication.

Por Caliendo, A M, Savara, A, An, D, DeVore, K, Kaplan, J C, D'Aquila, R T
Publicado em 1996

The isolation of a human Ig V lambda gene from a recombinant library of chromosome 22 and estimation of its copy number.

Por Anderson, M L, Szajnert, M F, Kaplan, J C, McColl, L, Young, B D
Publicado em 1984

Clustered somatic mutations in and around first exon of non-rearranged c-myc in Burkitt lymphoma with t(8;22) translocation.

Por Szajnert, M F, Saule, S, Bornkamm, G W, Wajcman, H, Lenoir, G M, Kaplan, J C
Publicado em 1987