MacRae C - Search Results

1

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: macrae c. Nat Genet. 1993 Apr;3(4):333-7. doi: 10.1038/ng0493-333. Nat Genet. 1993. PMID: 7981753

2

Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Watkins H, Seidman CE, MacRae C, Seidman JG, McKenna W. Watkins H, et al. Among authors: macrae c. Br Heart J. 1992 Jan;67(1):34-8. doi: 10.1136/hrt.67.1.34. Br Heart J. 1992. PMID: 1739523 Free PMC article. Review. No abstract available.

3

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE. Watkins H, et al. Among authors: macrae c. Nat Genet. 1995 Dec;11(4):434-7. doi: 10.1038/ng1295-434. Nat Genet. 1995. PMID: 7493025

4

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB 3rd, Cody RJ, Fishman MC, et al. Kass S, et al. Among authors: macrae c. Nat Genet. 1994 Aug;7(4):546-51. doi: 10.1038/ng0894-546. Nat Genet. 1994. PMID: 7951328

5

Assignment of the human a-tropomyosin gene TPM3 to 1q22-->q23 by fluorescence in situ hybridisation.

Wilton SD, Eyre H, Akkari PA, Watkins HC, MacRae C, Laing NG, Callen DC. Wilton SD, et al. Among authors: macrae c. Cytogenet Cell Genet. 1995;68(1-2):122-4. doi: 10.1159/000133905. Cytogenet Cell Genet. 1995. PMID: 7956350

6

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE. Thierfelder L, et al. Among authors: macrae c. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. PMID: 8205619

7

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A, et al. Thierfelder L, et al. Among authors: macrae c. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6270-4. doi: 10.1073/pnas.90.13.6270. Proc Natl Acad Sci U S A. 1993. PMID: 8327508 Free PMC article.

8

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.

Manolis EN, Yandavi N, Nadol JB Jr, Eavey RD, McKenna M, Rosenbaum S, Khetarpal U, Halpin C, Merchant SN, Duyk GM, MacRae C, Seidman CE, Seidman JG. Manolis EN, et al. Among authors: macrae c. Hum Mol Genet. 1996 Jul;5(7):1047-50. doi: 10.1093/hmg/5.7.1047. Hum Mol Genet. 1996. PMID: 8817345

9

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Siu BL, et al. Among authors: macrae c. Circulation. 1999 Mar 2;99(8):1022-6. doi: 10.1161/01.cir.99.8.1022. Circulation. 1999. PMID: 10051295

10

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.

Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ Jr, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Müehle G, Johnson W, McDonough B. Fatkin D, et al. Among authors: macrae c. N Engl J Med. 1999 Dec 2;341(23):1715-24. doi: 10.1056/NEJM199912023412302. N Engl J Med. 1999. PMID: 10580070 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

663 results

Search Page

Filters