Molecular genetics of neurological tumours.

Por Chung, R Y, Seizinger, B R
Publicado em 1992

Gene regulation by temperature-sensitive p53 mutants: identification of p53 response genes.

Por Buckbinder, L, Talbott, R, Seizinger, B R, Kley, N
Publicado em 1994

A (CA)n dinucleotide repeat assay for evaluating loss of allelic heterozygosity in small and archival human brain tumor specimens.

Por Louis, D. N., von Deimling, A., Seizinger, B. R.
Publicado em 1992

The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus.

Por Collins, F S, Ponder, B A, Seizinger, B R, Epstein, C J
Publicado em 1989

Repression of the basal c-fos promoter by wild-type p53.

Por Kley, N, Chung, R Y, Fay, S, Loeffler, J P, Seizinger, B R
Publicado em 1992

Molecular genetic approach to human meningioma: loss of genes on chromosome 22.

Por Seizinger, B R, de la Monte, S, Atkins, L, Gusella, J F, Martuza, R L
Publicado em 1987

Isolation and structure of a C-terminally amidated nonopioid peptide, amidorphin-(8-26), from bovine striatum: a major product of proenkephalin in brain but not in adrenal medulla.

Por Liebisch, D C, Weber, E, Kosicka, B, Gramsch, C, Herz, A, Seizinger, B R
Publicado em 1986

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms.

Por Larsson, C, Shepherd, J, Nakamura, Y, Blomberg, C, Weber, G, Werelius, B, Hayward, N, Teh, B, Tokino, T, Seizinger, B
Publicado em 1992

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

Por Fontaine, B, Rouleau, G A, Seizinger, B, Jewell, A F, Hanson, M P, Martuza, R L, Gusella, J F
Publicado em 1990

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Por Rouleau, G A, Seizinger, B R, Wertelecki, W, Haines, J L, Superneau, D W, Martuza, R L, Gusella, J F
Publicado em 1990

High frequency of inactivating mutations in the neurofibromatosis type 2 gene (NF2) in primary malignant mesotheliomas.

Por Bianchi, A B, Mitsunaga, S I, Cheng, J Q, Klein, W M, Jhanwar, S C, Seizinger, B, Kley, N, Klein-Szanto, A J, Testa, J R
Publicado em 1995

DNA linkage analysis in Von Recklinghausen neurofibromatosis.

Por Seizinger, B R, Rouleau, G, Lane, A H, Ozelius, L J, Faryniarz, A G, Iannazzi, J, Hobbs, W, Roy, J C, Falcone, B, Huson, S
Publicado em 1987

Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease.

Por Seizinger, B R, Smith, D I, Filling-Katz, M R, Neumann, H, Green, J S, Choyke, P L, Anderson, K M, Freiman, R N, Klauck, S M, Whaley, J
Publicado em 1991

Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)

Por Seizinger, B. R., Farmer, G. E., Haines, J. L., Ozelius, L. J., Anderson, K., Korf, B. R., Parry, D. M., Pericak-Vance, M. A., Mulvihill, J. J., Menon, A., Hobbs, W. J., Martuza, R. L., Gusella, J. F.
Publicado em 1989