These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
175 related articles for article (PubMed ID: 8698351)
21. Transthyretin isoleucine-122 mutation in African and American blacks. Afolabi I; Hamidi Asl K; Nakamura M; Jacobs P; Hendrie H; Benson MD Amyloid; 2000 Jun; 7(2):121-5. PubMed ID: 10842715 [TBL] [Abstract][Full Text] [Related]
22. A case of late onset cardiac amyloidosis with a new transthyretin variant (lysine 92). Saito F; Nakazato M; Akiyama H; Kitahara Y; Date Y; Iwasaki Y; Harasawa S; Hisaki R; Horie T; Kinukawa N; Watanabe T; Sakamaki T; Yagi H; Hoshii Y; Yutani C; Kanmatsuse K Hum Pathol; 2001 Feb; 32(2):237-9. PubMed ID: 11230714 [TBL] [Abstract][Full Text] [Related]
23. The amyloidogenic V122I transthyretin variant in elderly black Americans. Quarta CC; Buxbaum JN; Shah AM; Falk RH; Claggett B; Kitzman DW; Mosley TH; Butler KR; Boerwinkle E; Solomon SD N Engl J Med; 2015 Jan; 372(1):21-9. PubMed ID: 25551524 [TBL] [Abstract][Full Text] [Related]
24. Cardiac amyloidosis associated with the transthyretin Ile122 mutation in a Caucasian family. Hamidi Asl K; Nakamura M; Yamashita T; Benson MD Amyloid; 2001 Dec; 8(4):263-9. PubMed ID: 11791619 [TBL] [Abstract][Full Text] [Related]
25. Cardiac amyloidosis: report of a patient heterozygous for the transthyretin isoleucine 122 variant. Saraiva MJ; Sherman W; Marboe C; Figueira A; Costa P; de Freitas AF; Gawinowicz MA Scand J Immunol; 1990 Oct; 32(4):341-6. PubMed ID: 2237288 [TBL] [Abstract][Full Text] [Related]
26. Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis. Jacobson DR; Gertz MA; Buxbaum JN Hum Mutat; 1994; 3(4):399-401. PubMed ID: 8081397 [No Abstract] [Full Text] [Related]
27. Polymorphism of the thiopurine S-methyltransferase gene in African-Americans. Hon YY; Fessing MY; Pui CH; Relling MV; Krynetski EY; Evans WE Hum Mol Genet; 1999 Feb; 8(2):371-6. PubMed ID: 9931346 [TBL] [Abstract][Full Text] [Related]
28. Homozygosity for the V122I mutation in transthyretin is associated with earlier onset of cardiac amyloidosis in the African American population in the seventh decade of life. Reddi HV; Jenkins S; Theis J; Thomas BC; Connors LH; Van Rhee F; Highsmith WE J Mol Diagn; 2014 Jan; 16(1):68-74. PubMed ID: 24184229 [TBL] [Abstract][Full Text] [Related]
29. Functional variation of the transthyretin gene among human populations and its correlation with amyloidosis phenotypes. Polimanti R; Di Girolamo M; Manfellotto D; Fuciarelli M Amyloid; 2013 Dec; 20(4):256-62. PubMed ID: 24111657 [TBL] [Abstract][Full Text] [Related]
30. Prevalence and Outcomes of p.Val142Ile Chandrashekar P; Alhuneafat L; Mannello M; Al-Rashdan L; Kim MM; Dungu J; Alexander K; Masri A Circ Genom Precis Med; 2021 Oct; 14(5):e003356. PubMed ID: 34461737 [TBL] [Abstract][Full Text] [Related]
31. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant. Hesse A; Altland K; Linke RP; Almeida MR; Saraiva MJ; Steinmetz A; Maisch B Br Heart J; 1993 Aug; 70(2):111-5. PubMed ID: 8038017 [TBL] [Abstract][Full Text] [Related]
32. Association of Transthyretin Val122Ile Variant With Incident Heart Failure Among Black Individuals. Parcha V; Malla G; Irvin MR; Armstrong ND; Judd SE; Lange LA; Maurer MS; Levitan EB; Goyal P; Arora G; Arora P JAMA; 2022 Apr; 327(14):1368-1378. PubMed ID: 35377943 [TBL] [Abstract][Full Text] [Related]
33. Transthyretin Cardiac Amyloidosis in Black Americans. Shah KB; Mankad AK; Castano A; Akinboboye OO; Duncan PB; Fergus IV; Maurer MS Circ Heart Fail; 2016 Jun; 9(6):e002558. PubMed ID: 27188913 [TBL] [Abstract][Full Text] [Related]
34. A double-variant transthyretin allele (Ser 6, Ile 33) in the Israeli patient "SKO" with familial amyloidotic polyneuropathy. Jacobson DR; Buxbaum JN Hum Mutat; 1994; 3(3):254-60. PubMed ID: 8019560 [TBL] [Abstract][Full Text] [Related]
35. Three siblings of familial amyloid cardiomyopathy with isoleucine-50 transthyretin mutation. Sadamatsu K; Hayashi Y; Nakamura M Int J Cardiol; 1997 Sep; 61(2):151-5. PubMed ID: 9314208 [TBL] [Abstract][Full Text] [Related]
36. Transthyretin V122I in African Americans with congestive heart failure. Buxbaum J; Jacobson DR; Tagoe C; Alexander A; Kitzman DW; Greenberg B; Thaneemit-Chen S; Lavori P J Am Coll Cardiol; 2006 Apr; 47(8):1724-5. PubMed ID: 16631014 [No Abstract] [Full Text] [Related]
37. A new isoleucine substitution of Val-20 in transthyretin tetramers selectively impairs dimer-dimer contacts and causes systemic amyloidosis. Jenne DE; Denzel K; Blätzinger P; Winter P; Obermaier B; Linke RP; Altland K Proc Natl Acad Sci U S A; 1996 Jun; 93(13):6302-7. PubMed ID: 8692810 [TBL] [Abstract][Full Text] [Related]
38. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans. Monaghan KG; Rybicki BA; Shurafa M; Feldman GL Am J Hematol; 1998 Jul; 58(3):213-7. PubMed ID: 9662273 [TBL] [Abstract][Full Text] [Related]
39. A transthyretin variant, Asp18Asn, associated with amyloid cardiomyopathy: a new African-American variant? Quarta CC; Falk RH Amyloid; 2012 Dec; 19(4):204-7. PubMed ID: 23126592 [TBL] [Abstract][Full Text] [Related]