Tynan K - Search Results

1

Unique sequence STSs for 21 cytogenetically mapped loci on human chromosome 19.

Mohrenweiser HW, Tsujimoto S, Tynan K, Lamerdin J, Carrano AV. Mohrenweiser HW, et al. Among authors: tynan k. Cytogenet Cell Genet. 1995;71(1):58-61. doi: 10.1159/000134063. Cytogenet Cell Genet. 1995. PMID: 7606929

2

Assembly and analysis of cosmid contigs in the CEA-gene family region of human chromosome 19.

Tynan K, Olsen A, Trask B, de Jong P, Thompson J, Zimmermann W, Carrano A, Mohrenweiser H. Tynan K, et al. Nucleic Acids Res. 1992 Apr 11;20(7):1629-36. doi: 10.1093/nar/20.7.1629. Nucleic Acids Res. 1992. PMID: 1579453 Free PMC article.

3

Order and genomic distances among members of the carcinoembryonic antigen (CEA) gene family determined by fluorescence in situ hybridization.

Brandriff BF, Gordon LA, Tynan KT, Olsen AS, Mohrenweiser HW, Fertitta A, Carrano AV, Trask BJ. Brandriff BF, et al. Among authors: tynan kt. Genomics. 1992 Apr;12(4):773-9. doi: 10.1016/0888-7543(92)90308-f. Genomics. 1992. PMID: 1572650

4

Organization of the multiple polymorphic sites of the D19S11 locus within a 650-kb cosmid contig.

Tynan K, Hoffman SM, Tsujimoto S, Brandriff B, Gordon L, Carrano AV, Mohrenweiser HW. Tynan K, et al. Genomics. 1993 Aug;17(2):316-23. doi: 10.1006/geno.1993.1327. Genomics. 1993. PMID: 8406482

5

Assignment of the gene encoding DNA ligase I to human chromosome 19q13.2-13.3.

Barnes DE, Kodama K, Tynan K, Trask BJ, Christensen M, De Jong PJ, Spurr NK, Lindahl T, Mohrenweiser HW. Barnes DE, et al. Among authors: tynan k. Genomics. 1992 Jan;12(1):164-6. doi: 10.1016/0888-7543(92)90422-o. Genomics. 1992. PMID: 1733856

6

Mutation screening of complete fibrillin-1 coding sequence: report of five new mutations, including two in 8-cysteine domains.

Tynan K, Comeau K, Pearson M, Wilgenbus P, Levitt D, Gasner C, Berg MA, Miller DC, Francke U. Tynan K, et al. Hum Mol Genet. 1993 Nov;2(11):1813-21. doi: 10.1093/hmg/2.11.1813. Hum Mol Genet. 1993. PMID: 8281141

7

Long-range chromosomal mapping of the carcinoembryonic antigen (CEA) gene family cluster.

Thompson J, Zimmermann W, Osthus-Bugat P, Schleussner C, Eades-Perner AM, Barnert S, Von Kleist S, Willcocks T, Craig I, Tynan K, et al. Thompson J, et al. Among authors: tynan k. Genomics. 1992 Apr;12(4):761-72. doi: 10.1016/0888-7543(92)90307-e. Genomics. 1992. PMID: 1572649 Free article.

8

A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection.

Francke U, Berg MA, Tynan K, Brenn T, Liu W, Aoyama T, Gasner C, Miller DC, Furthmayr H. Francke U, et al. Among authors: tynan k. Am J Hum Genet. 1995 Jun;56(6):1287-96. Am J Hum Genet. 1995. PMID: 7762551 Free PMC article.

9

Missense mutations impair intracellular processing of fibrillin and microfibril assembly in Marfan syndrome.

Aoyama T, Tynan K, Dietz HC, Francke U, Furthmayr H. Aoyama T, et al. Among authors: tynan k. Hum Mol Genet. 1993 Dec;2(12):2135-40. doi: 10.1093/hmg/2.12.2135. Hum Mol Genet. 1993. PMID: 8111384

10

Low-dose naltrexone in the treatment of fibromyalgia: A systematic review and narrative synthesis.

Aitcheson N, Lin Z, Tynan K. Aitcheson N, et al. Among authors: tynan k. Aust J Gen Pract. 2023 Apr;52(4):189-195. doi: 10.31128/AJGP-09-22-6564. Aust J Gen Pract. 2023. PMID: 37021443 Free article.

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