Tsui LC - Search Results

1

Smooth pursuit eye movements in the evaluation of famotidine adjunctive therapy of schizophrenia: a preliminary report.

Rosenberg PB, Rosse RB, Johri SK, Kendrick K, Fay-McCarthy M, Collins JP Jr, Tsui LC, Wyatt RJ, Deutsch SI. Rosenberg PB, et al. Among authors: tsui lc. Clin Neuropharmacol. 1996 Jun;19(3):276-81. doi: 10.1097/00002826-199619030-00011. Clin Neuropharmacol. 1996. PMID: 8726548 Clinical Trial.

2

Famotidine adjunctive pharmacotherapy of schizophrenia: a case report.

Rosse RB, Kendrick K, Tsui LC, Fay-McCarthy M, Collins JP Jr, Rosenberg P, Wyatt RJ, Deutsch SI. Rosse RB, et al. Among authors: tsui lc. Clin Neuropharmacol. 1995 Aug;18(4):369-74. doi: 10.1097/00002826-199508000-00009. Clin Neuropharmacol. 1995. PMID: 8665550

3

An open-label study of the therapeutic efficacy of high-dose famotidine adjuvant pharmacotherapy in schizophrenia: preliminary evidence for treatment efficacy.

Rosse RB, Kendrick K, Fay-McCarthy M, Prell GD, Rosenberg P, Tsui LC, Wyatt RJ, Deutsch SI. Rosse RB, et al. Among authors: tsui lc. Clin Neuropharmacol. 1996 Aug;19(4):341-8. doi: 10.1097/00002826-199619040-00007. Clin Neuropharmacol. 1996. PMID: 8828997 Clinical Trial.

4

Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Palmer SE, Scherer SW, Kukolich M, Wijsman EM, Tsui LC, Stephens K, Evans JP. Palmer SE, et al. Among authors: tsui lc. Am J Hum Genet. 1994 Jul;55(1):21-6. Am J Hum Genet. 1994. PMID: 7912888 Free PMC article.

5

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.

Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S, Cobben JM, Hudgins L, Evans JP, Tsui LC. Crackower MA, et al. Among authors: tsui lc. Hum Mol Genet. 1996 May;5(5):571-9. doi: 10.1093/hmg/5.5.571. Hum Mol Genet. 1996. PMID: 8733122

6

Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families.

Iles DE, Lehmann-Horn F, Scherer SW, Tsui LC, Olde Weghuis D, Suijkerbuijk RF, Heytens L, Mikala G, Schwartz A, Ellis FR, et al. Iles DE, et al. Among authors: tsui lc. Hum Mol Genet. 1994 Jun;3(6):969-75. doi: 10.1093/hmg/3.6.969. Hum Mol Genet. 1994. PMID: 7951247

7

Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly.

Roessler E, Ward DE, Gaudenz K, Belloni E, Scherer SW, Donnai D, Siegel-Bartelt J, Tsui LC, Muenke M. Roessler E, et al. Among authors: tsui lc. Hum Genet. 1997 Aug;100(2):172-81. doi: 10.1007/s004390050486. Hum Genet. 1997. PMID: 9254845

8

Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agents.

Thacker J, Tambini CE, Simpson PJ, Tsui LC, Scherer SW. Thacker J, et al. Among authors: tsui lc. Hum Mol Genet. 1995 Jan;4(1):113-20. doi: 10.1093/hmg/4.1.113. Hum Mol Genet. 1995. PMID: 7711722

9

Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient.

Alley TL, Gray BA, Lee SH, Scherer SW, Tsui LC, Tint GS, Williams CA, Zori R, Wallace MR. Alley TL, et al. Among authors: tsui lc. Am J Hum Genet. 1995 Jun;56(6):1411-6. Am J Hum Genet. 1995. PMID: 7762564 Free PMC article.

10

Refined localization and yeast artificial chromosome (YAC) contig--mapping of genes and DNA segments in the 7q21-q32 region.

Scherer SW, Rommens JM, Soder S, Wong E, Plavsic N, Tompkins BJ, Beattie A, Kim J, Tsui LC. Scherer SW, et al. Among authors: tsui lc. Hum Mol Genet. 1993 Jun;2(6):751-60. doi: 10.1093/hmg/2.6.751. Hum Mol Genet. 1993. PMID: 8353494

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