"Copy and paste" transposable elements in the human genome.

Por Kazazian, H H, Scott, A F
Publicado em 1993

Two additional potential retrotransposons isolated from a human L1 subfamily that contains an active retrotransposable element.

Por Dombroski, B A, Scott, A F, Kazazian, H H
Publicado em 1993

DNA restriction endonuclease analysis for localization of human beta- and delta-globin genes on chromosome 11.

Por Scott, A F, Phillips, J A, Migeon, B R
Publicado em 1979

Amplified DNA in Y1 mouse adrenal tumor cells: isolation of cDNAs complementary to an amplified c-Ki-ras gene and localization of homologous sequences to mouse chromosome 6.

Por George, D L, Scott, A F, de Martinville, B, Francke, U
Publicado em 1984

Structure and expression of amplified cKi-ras gene sequences in Y1 mouse adrenal tumor cells.

Por George, D L, Scott, A F, Trusko, S, Glick, B, Ford, E, Dorney, D J
Publicado em 1985

In vitro galactosylation of a 110-kDa glycoprotein by an endogenous cell surface galactosyltransferase correlates with the invasiveness of adrenal carcinoma cells.

Por Penno, M B, Passaniti, A, Fridman, R, Hart, G W, Jordan, C, Kumar, S, Scott, A F
Publicado em 1989

Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.

Por Phillips, J A, Panny, S R, Kazazian, H H, Boehm, C D, Scott, A F, Smith, K D
Publicado em 1980

beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.

Por Antonarakis, S E, Irkin, S H, Cheng, T C, Scott, A F, Sexton, J P, Trusko, S P, Charache, S, Kazazian, H H
Publicado em 1984

An in vivo assay for the reverse transcriptase of human retrotransposon L1 in Saccharomyces cerevisiae.

Por Dombroski, B A, Feng, Q, Mathias, S L, Sassaman, D M, Scott, A F, Kazazian, H H, Boeke, J D
Publicado em 1994

The molecular basis of hemoglobin Grady.

Por Scott, A F, Phillips, J A, Young, K E, Kazazian, H H, Smith, K D, Charache, S, Clegg, J B
Publicado em 1981

Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosis.

Por Panny, S R, Scott, A F, Smith, K D, Phillips, J A, Kazazian, H H, Talbot, C C, Boehm, C D
Publicado em 1981

Haplotype Diversity in 11 Candidate Genes Across Four Populations

Por Beaty, T. H., Fallin, M. D., Hetmanski, J. B., McIntosh, I., Chong, S. S., Ingersoll, R., Sheng, X., Chakraborty, R., Scott, A. F.
Publicado em 2005

High throughput SNP and expression analyses of candidate genes for non‐syndromic oral clefts

Por Park, J W, Cai, J, McIntosh, I, Jabs, E W, Fallin, M D, Ingersoll, R, Hetmanski, J B, Vekemans, M, Attie‐Bitach, T, Lovett, M, Scott, A F, Beaty, T H
Publicado em 2006

FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing.

Por Meyers, G. A., Day, D., Goldberg, R., Daentl, D. L., Przylepa, K. A., Abrams, L. J., Graham, J. M., Feingold, M., Moeschler, J. B., Rawnsley, E., Scott, A. F., Jabs, E. W.
Publicado em 1996