Stenzel TT - Search Results

1

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.

Berg JN, Gallione CJ, Stenzel TT, Johnson DW, Allen WP, Schwartz CE, Jackson CE, Porteous ME, Marchuk DA. Berg JN, et al. Among authors: stenzel tt. Am J Hum Genet. 1997 Jul;61(1):60-7. doi: 10.1086/513903. Am J Hum Genet. 1997. PMID: 9245985 Free PMC article.

2

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Johnson DW, Berg JN, Baldwin MA, Gallione CJ, Marondel I, Yoon SJ, Stenzel TT, Speer M, Pericak-Vance MA, Diamond A, Guttmacher AE, Jackson CE, Attisano L, Kucherlapati R, Porteous ME, Marchuk DA. Johnson DW, et al. Among authors: stenzel tt. Nat Genet. 1996 Jun;13(2):189-95. doi: 10.1038/ng0696-189. Nat Genet. 1996. PMID: 8640225

3

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles.

Gallione CJ, Klaus DJ, Yeh EY, Stenzel TT, Xue Y, Anthony KB, McAllister KA, Baldwin MA, Berg JN, Lux A, Smith JD, Vary CP, Craigen WJ, Westermann CJ, Warner ML, Miller YE, Jackson CE, Guttmacher AE, Marchuk DA. Gallione CJ, et al. Among authors: stenzel tt. Hum Mutat. 1998;11(4):286-94. doi: 10.1002/(SICI)1098-1004(1998)11:4<286::AID-HUMU6>3.0.CO;2-B. Hum Mutat. 1998. PMID: 9554745

4

Cytogenetic and molecular analysis of an unusual case of acute promyelocytic leukemia with a t(15;17;17)(q22;q23;q21).

Tirado CA, Golembiewski-Ruiz V, Horvatinovich J, Moore JO, Buckley PJ, Stenzel TT, Goodman BK. Tirado CA, et al. Among authors: stenzel tt. Cancer Genet Cytogenet. 2003 Aug;145(1):31-7. doi: 10.1016/s0165-4608(03)00027-x. Cancer Genet Cytogenet. 2003. PMID: 12885460

5

Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in a case of acute monoblastic leukemia with tetrasomy 8.

Zhang XX, Robinson LJ, Stenzel TT, Qumsiyeh MB. Zhang XX, et al. Among authors: stenzel tt. Cancer Genet Cytogenet. 1999 Aug;113(1):9-13. doi: 10.1016/s0165-4608(98)00278-7. Cancer Genet Cytogenet. 1999. PMID: 10459339

6

Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutations.

Bernacki SH, Farkas DH, Shi W, Chan V, Liu Y, Beck JC, Bailey KS, Pratt VM, Monaghan KG, Matteson KJ, Schaefer FV, Friez M, Shrimpton AE, Stenzel TT. Bernacki SH, et al. Among authors: stenzel tt. Arch Pathol Lab Med. 2003 Dec;127(12):1565-72. doi: 10.5858/2003-127-1565-BSTFDO. Arch Pathol Lab Med. 2003. PMID: 14632577 Free article.

7

PTEN gene mutations are seen in high-grade but not in low-grade gliomas.

Rasheed BK, Stenzel TT, McLendon RE, Parsons R, Friedman AH, Friedman HS, Bigner DD, Bigner SH. Rasheed BK, et al. Among authors: stenzel tt. Cancer Res. 1997 Oct 1;57(19):4187-90. Cancer Res. 1997. PMID: 9331072

8

Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization.

Bigner SH, Matthews MR, Rasheed BK, Wiltshire RN, Friedman HS, Friedman AH, Stenzel TT, Dawes DM, McLendon RE, Bigner DD. Bigner SH, et al. Among authors: stenzel tt. Am J Pathol. 1999 Aug;155(2):375-86. doi: 10.1016/S0002-9440(10)65134-6. Am J Pathol. 1999. PMID: 10433931 Free PMC article.

9

Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet-derived growth factor receptor-alpha genes in a patient with atypical chronic myeloid leukemia.

Safley AM, Sebastian S, Collins TS, Tirado CA, Stenzel TT, Gong JZ, Goodman BK. Safley AM, et al. Among authors: stenzel tt. Genes Chromosomes Cancer. 2004 May;40(1):44-50. doi: 10.1002/gcc.20014. Genes Chromosomes Cancer. 2004. PMID: 15034867

10

Characterization of publicly available lymphoblastoid cell lines for disease-associated mutations in 11 genes.

Bernacki SH, Beck JC, Muralidharan K, Schaefer FV, Shrimpton AE, Richie KL, Levin BC, Pont-Kingdon G, Stenzel TT. Bernacki SH, et al. Among authors: stenzel tt. Clin Chem. 2005 Nov;51(11):2156-9. doi: 10.1373/clinchem.2005.048686. Clin Chem. 2005. PMID: 16244288 No abstract available.

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