Dinucleotide repeat polymorphism at the ABL locus (9q34)

Bằng Kwiatkowski, D.J.
Được phát hành 1991

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

Bằng Kwiatkowski, D.J., Perman, S.
Được phát hành 1991

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

Bằng Youssoufian, H, McAfee, M, Kwiatkowski, D J
Được phát hành 1990

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

Bằng Glück, U, Kwiatkowski, D J, Ben-Ze'ev, A
Được phát hành 1993

Gelsolin is a downstream effector of rac for fibroblast motility.

Bằng Azuma, T, Witke, W, Stossel, T P, Hartwig, J H, Kwiatkowski, D J
Được phát hành 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.

Bằng Kwiatkowski, D J, Aklog, L, Ledbetter, D H, Morton, C C
Được phát hành 1990

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

Bằng Bjornsson, J., Short, M. P., Kwiatkowski, D. J., Henske, E. P.
Được phát hành 1996

A diagnostic algorithm for enhanced detection of mosaic tuberous sclerosis complex in adults

Bằng Treichel, A.M., Kwiatkowski, D.J., Moss, J., Darling, T.N.
Xuất bản năm Br J Dermatol (2019)

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

Bằng Kwiatkowski, D J, Ozelius, L, Schuback, D, Gusella, J, Breakefield, X O
Được phát hành 1989

Localization of gelsolin proximal to ABL on chromosome 9.

Bằng Kwiatkowski, D J, Westbrook, C A, Bruns, G A, Morton, C C
Được phát hành 1988

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

Bằng Kwiatkowski, D J, Dib, C, Slaugenhaupt, S A, Povey, S, Gusella, J F, Haines, J L
Được phát hành 1993

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

Bằng Nellist, M, Brook-Carter, P T, Connor, J M, Kwiatkowski, D J, Johnson, P, Sampson, J R
Được phát hành 1993

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

Bằng Wiens, A, Marles, S, Safneck, J, Kwiatkowski, D J, Maury, C P, Zelinski, T, Philipps, S, Ekins, M B, Greenberg, C R
Được phát hành 1992

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

Bằng Kwiatkowski, D J, Ozelius, L, Kramer, P L, Perman, S, Schuback, D E, Gusella, J F, Fahn, S, Breakefield, X O
Được phát hành 1991

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

Bằng 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
Được phát hành 1992

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

Bằng Henske, E. P., Scheithauer, B. W., Short, M. P., Wollmann, R., Nahmias, J., Hornigold, N., van Slegtenhorst, M., Welsh, C. T., Kwiatkowski, D. J.
Được phát hành 1996

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

Bằng Haines, J L, Short, M P, Kwiatkowski, D J, Jewell, A, Andermann, E, Bejjani, B, Yang, C H, Gusella, J F, Amos, J A
Được phát hành 1991

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

Bằng 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.
Được phát hành 1997

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

Bằng 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
Được phát hành 1997