Clarke JT - Search Results

1

A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studies.

Akerman BR, Zielenski J, Triggs-Raine BL, Prence EM, Natowicz MR, Lim-Steele JS, Kaback MM, Mules EH, Thomas GH, Clarke JT, et al. Akerman BR, et al. Among authors: clarke jt. Hum Mutat. 1992;1(4):303-9. doi: 10.1002/humu.1380010407. Hum Mutat. 1992. PMID: 1301938

2

Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease.

Triggs-Raine BL, Akerman BR, Clarke JT, Gravel RA. Triggs-Raine BL, et al. Among authors: clarke jt. Am J Hum Genet. 1991 Nov;49(5):1041-54. Am J Hum Genet. 1991. PMID: 1833974 Free PMC article.

3

Screening for carriers of Tay-Sachs disease among Ashkenazi Jews. A comparison of DNA-based and enzyme-based tests.

Triggs-Raine BL, Feigenbaum AS, Natowicz M, Skomorowski MA, Schuster SM, Clarke JT, Mahuran DJ, Kolodny EH, Gravel RA. Triggs-Raine BL, et al. Among authors: clarke jt. N Engl J Med. 1990 Jul 5;323(1):6-12. doi: 10.1056/NEJM199007053230102. N Engl J Med. 1990. PMID: 2355960 Free article.

4

W474C amino acid substitution affects early processing of the alpha-subunit of beta-hexosaminidase A and is associated with subacute G(M2) gangliosidosis.

Petroulakis E, Cao Z, Clarke JT, Mahuran DJ, Lee G, Triggs-Raine B. Petroulakis E, et al. Among authors: clarke jt. Hum Mutat. 1998;11(6):432-42. doi: 10.1002/(SICI)1098-1004(1998)11:6<432::AID-HUMU3>3.0.CO;2-Z. Hum Mutat. 1998. PMID: 9603435

5

Prenatal exclusion of Tay-Sachs disease by DNA analysis.

Triggs-Raine BL, Archibald A, Gravel RA, Clarke JT. Triggs-Raine BL, et al. Among authors: clarke jt. Lancet. 1990 May 12;335(8698):1164. doi: 10.1016/0140-6736(90)91170-f. Lancet. 1990. PMID: 1971898 No abstract available.

6

Genotype-phenotype pitfalls in Gaucher disease.

Strasberg PM, Triggs-Raine BL, Warren IB, Skomorowski MA, McInnes B, Becker LE, Callahan JW, Clarke JT. Strasberg PM, et al. Among authors: clarke jt. J Clin Lab Anal. 1994;8(4):228-36. doi: 10.1002/jcla.1860080409. J Clin Lab Anal. 1994. PMID: 7931818 Review.

7

Rapid nonradioactive tracer method for detecting carriers of the major Ashkenazi Jewish Tay-Sachs disease mutations.

Strasberg PM, Clarke JT. Strasberg PM, et al. Among authors: clarke jt. Clin Chem. 1992 Nov;38(11):2249-55. Clin Chem. 1992. PMID: 1424119

8

Identification and expression of eight novel mutations among non-Jewish patients with Canavan disease.

Kaul R, Gao GP, Matalon R, Aloya M, Su Q, Jin M, Johnson AB, Schutgens RB, Clarke JT. Kaul R, et al. Among authors: clarke jt. Am J Hum Genet. 1996 Jul;59(1):95-102. Am J Hum Genet. 1996. PMID: 8659549 Free PMC article.

9

Tay-Sachs disease carrier screening: follow-up of a case-finding approach.

Clarke JT, Skomorowski MA, Zuker S. Clarke JT, et al. Am J Med Genet. 1989 Dec;34(4):601-5. doi: 10.1002/ajmg.1320340430. Am J Med Genet. 1989. PMID: 2624277

10

First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase A.

Callahan JW, Archibald A, Skomorowski MA, Shuman C, Clarke JT. Callahan JW, et al. Among authors: clarke jt. Clin Biochem. 1990 Dec;23(6):533-6. doi: 10.1016/0009-9120(90)80045-k. Clin Biochem. 1990. PMID: 2149678

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