Dinucleotide repeat polymorphism at the ABL locus (9q34)

Por Kwiatkowski, D.J.
Publicado em 1991

Dinucleotide repeat polymorphism at the GSN locus (9q32–34)

Por Kwiatkowski, D.J., Perman, S.
Publicado em 1991

Cloning and chromosomal localization of the human cytoskeletal alpha-actinin gene reveals linkage to the beta-spectrin gene.

Por Youssoufian, H, McAfee, M, Kwiatkowski, D J
Publicado em 1990

Suppression of tumorigenicity in simian virus 40-transformed 3T3 cells transfected with alpha-actinin cDNA.

Por Glück, U, Kwiatkowski, D J, Ben-Ze'ev, A
Publicado em 1993

Gelsolin is a downstream effector of rac for fibroblast motility.

Por Azuma, T, Witke, W, Stossel, T P, Hartwig, J H, Kwiatkowski, D J
Publicado em 1998

Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndrome.

Por Kwiatkowski, D J, Aklog, L, Ledbetter, D H, Morton, C C
Publicado em 1990

Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features.

Por Bjornsson, J., Short, M. P., Kwiatkowski, D. J., Henske, E. P.
Publicado em 1996

The gelsolin (GSN) cDNA clone, from 9q32-34, identifies BclI and StuI RFLPs.

Por Kwiatkowski, D J, Ozelius, L, Schuback, D, Gusella, J, Breakefield, X O
Publicado em 1989

Localization of gelsolin proximal to ABL on chromosome 9.

Por Kwiatkowski, D J, Westbrook, C A, Bruns, G A, Morton, C C
Publicado em 1988

An index marker map of chromosome 9 provides strong evidence for positive interference.

Por Kwiatkowski, D J, Dib, C, Slaugenhaupt, S A, Povey, S, Gusella, J F, Haines, J L
Publicado em 1993

Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1).

Por Nellist, M, Brook-Carter, P T, Connor, J M, Kwiatkowski, D J, Johnson, P, Sampson, J R
Publicado em 1993

Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.

Por Wiens, A, Marles, S, Safneck, J, Kwiatkowski, D J, Maury, C P, Zelinski, T, Philipps, S, Ekins, M B, Greenberg, C R
Publicado em 1992

Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.

Por Kwiatkowski, D J, Ozelius, L, Kramer, P L, Perman, S, Schuback, D E, Gusella, J F, Fahn, S, Breakefield, X O
Publicado em 1991

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.

Por Northrup, H, Kwiatkowski, D J, Roach, E S, Dobyns, W B, Lewis, R A, Herman, G E, Rodriguez, E, Daiger, S P, Blanton, S H
Publicado em 1992

Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.

Por Henske, E. P., Scheithauer, B. W., Short, M. P., Wollmann, R., Nahmias, J., Hornigold, N., van Slegtenhorst, M., Welsh, C. T., Kwiatkowski, D. J.
Publicado em 1996

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.

Por Haines, J L, Short, M P, Kwiatkowski, D J, Jewell, A, Andermann, E, Bejjani, B, Yang, C H, Gusella, J F, Amos, J A
Publicado em 1991

Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors.

Por Henske, E. P., Wessner, L. L., Golden, J., Scheithauer, B. W., Vortmeyer, A. O., Zhuang, Z., Klein-Szanto, A. J., Kwiatkowski, D. J., Yeung, R. S.
Publicado em 1997

Fine mapping of the nail-patella syndrome locus at 9q34.

Por McIntosh, I, Clough, M V, Schäffer, A A, Puffenberger, E G, Horton, V K, Peters, K, Abbott, M H, Roig, C M, Cutone, S, Ozelius, L, Kwiatkowski, D J, Pyeritz, R E, Brown, L J, Pauli, R M, McCormick, M K, Francomano, C A
Publicado em 1997