Partial mRNA sequences for human A alpha, B beta, and gamma fibrinogen chains: evolutionary and functional implications.

Por Kant, J A, Lord, S T, Crabtree, G R
Publicado em 1983

BIOLOGIC DIVERSITY OF POLYOMAVIRUS BK GENOMIC SEQUENCES: IMPLICATIONS FOR MOLECULAR DIAGNOSTIC LABORATORIES

Por Luo, C, Bueno, M, Kant, J, Randhawa, P
Publicado em 2008

Molecular resemblance of an AIDS-associated lymphoma and endemic Burkitt lymphomas: implications for their pathogenesis.

Por Haluska, F G, Russo, G, Kant, J, Andreef, M, Croce, C M
Publicado em 1989

Absence of t(14;18) major and minor breakpoints and of Bcl-2 protein overproduction in Reed-Sternberg cells of Hodgkin's disease.

Por Louie, D. C., Kant, J. A., Brooks, J. J., Reed, J. C.
Publicado em 1991

Impact of Genomic Sequence Variability on Quantitative PCR Assays for Diagnosis of Polyomavirus BK Infection

Por Randhawa, P., Kant, J., Shapiro, R., Tan, H., Basu, A., Luo, C.
Publicado em 2011

Microencephaly in fetal piglets following in utero inoculation of Zika virus

Por Wichgers Schreur, P. J., van Keulen, L., Anjema, D., Kant, J., Kortekaas, J.
Publicado no Emerg Microbes Infect (2018)

Detection of CD2 polymorphism on chromosome 1 with EcoRI

Por Malter, J.S., Moolten, D.N., Alahari, S.K., Makni, H., Kant, J.A., Kamoun, M.
Publicado em 1990

Clonal analysis of solitary follicular nodules in the thyroid.

Por Hicks, D. G., LiVolsi, V. A., Neidich, J. A., Puck, J. M., Kant, J. A.
Publicado em 1990

In vivo treatment of human leukemia in a scid mouse model with c-myb antisense oligodeoxynucleotides.

Por Ratajczak, M Z, Kant, J A, Luger, S M, Hijiya, N, Zhang, J, Zon, G, Gewirtz, A M
Publicado em 1992

Paternal transmission of congenital myotonic dystrophy.

Por Bergoffen, J, Kant, J, Sladky, J, McDonald-McGinn, D, Zackai, E H, Fischbeck, K H
Publicado em 1994

Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion.

Por Kant, J A, Fornace, A J, Saxe, D, Simon, M I, McBride, O W, Crabtree, G R
Publicado em 1985

Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis

Por Pfützer, R, Myers, E, Applebaum-Shapiro, S, Finch, R, Ellis, I, Neoptolemos, J, Kant, J A, Whitcomb, D C
Publicado em 2002

Biologic and therapeutic significance of MYB expression in human melanoma.

Por Hijiya, N, Zhang, J, Ratajczak, M Z, Kant, J A, DeRiel, K, Herlyn, M, Zon, G, Gewirtz, A M
Publicado em 1994

Promoter region of interleukin-2 gene undergoes chromatin structure changes and confers inducibility on chloramphenicol acetyltransferase gene during activation of T cells.

Por Siebenlist, U, Durand, D B, Bressler, P, Holbrook, N J, Norris, C A, Kamoun, M, Kant, J A, Crabtree, G R
Publicado em 1986

Genetic heterogeneity in hereditary breast cancer: role of BRCA1 and BRCA2.

Por Rebbeck, T. R., Couch, F. J., Kant, J., Calzone, K., DeShano, M., Peng, Y., Chen, K., Garber, J. E., Weber, B. L.
Publicado em 1996

Seminoma in a postmenopausal woman with a Y;15 translocation in peripheral blood lymphocytes and a t(Y;15)/45,X Turner mosaic pattern in skin fibroblasts.

Por Hoshi, N, Fujita, M, Mikuni, M, Fujino, T, Okuyama, K, Handa, Y, Yamada, H, Sagawa, T, Hareyama, H, Nakahori, Y, Fujieda, K, Kant, J A, Nagashima, K, Fujimoto, S
Publicado em 1998