Nafa K - Search Results

1

Validation of a High-Sensitivity Assay for Detection of Chimeric Antigen Receptor T-Cell Vectors Using Low-Partition Digital PCR Technology.

Arcila ME, Patel U, Momeni-Boroujeni A, Yao J, Chan R, Chan J, Rijo I, Yu W, Chaves N, Patel H, Kakadiya S, Lachhander S, Senechal B, Riviere IC, Wang X, Sadelain M, Nafa K, Salazar P, Palomba L, Curran KJ, Park JH, Daniyan A, Borsu L. Arcila ME, et al. Among authors: nafa k. J Mol Diagn. 2023 Sep;25(9):634-645. doi: 10.1016/j.jmoldx.2023.06.002. Epub 2023 Jun 16. J Mol Diagn. 2023. PMID: 37330049 Free PMC article.

2

Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type.

Nafa K, Mason PJ, Hillmen P, Luzzatto L, Bessler M. Nafa K, et al. Blood. 1995 Dec 15;86(12):4650-5. Blood. 1995. PMID: 8541557 Free article.

3

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.

Nafa K, Reghis A, Osmani N, Baghli L, Aït-Abbes H, Benabadji M, Kaplan JC, Vulliamy T, Luzzatto L. Nafa K, et al. Hum Genet. 1994 Nov;94(5):513-7. doi: 10.1007/BF00211017. Hum Genet. 1994. PMID: 7959686

4

Unique de novo mutation of BRCA2 in a woman with early onset breast cancer.

Robson M, Scheuer L, Nafa K, Ellis N, Offit K. Robson M, et al. Among authors: nafa k. J Med Genet. 2002 Feb;39(2):126-8. doi: 10.1136/jmg.39.2.126. J Med Genet. 2002. PMID: 11836363 Free PMC article. No abstract available.

5

Prediction of germline mutations and cancer risk in the Lynch syndrome.

Chen S, Wang W, Lee S, Nafa K, Lee J, Romans K, Watson P, Gruber SB, Euhus D, Kinzler KW, Jass J, Gallinger S, Lindor NM, Casey G, Ellis N, Giardiello FM, Offit K, Parmigiani G; Colon Cancer Family Registry. Chen S, et al. Among authors: nafa k. JAMA. 2006 Sep 27;296(12):1479-87. doi: 10.1001/jama.296.12.1479. JAMA. 2006. PMID: 17003396 Free PMC article.

6

A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A.

Nafa K, Baudis M, Deburgrave N, Bardin JM, Sultan Y, Kaplan JC, Delpech M. Nafa K, et al. Hum Mutat. 1992;1(1):77-8. doi: 10.1002/humu.1380010114. Hum Mutat. 1992. PMID: 1301194 No abstract available.

7

G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.

Nafa K, Reghis A, Osmani N, Baghli L, Benabadji M, Kaplan JC, Vulliamy TJ, Luzzatto L. Nafa K, et al. Hum Mol Genet. 1993 Jan;2(1):81-2. doi: 10.1093/hmg/2.1.81. Hum Mol Genet. 1993. PMID: 8490627 No abstract available.

8

Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH.

Peterlongo P, Mitra N, Chuai S, Kirchhoff T, Palmer C, Huang H, Nafa K, Offit K, Ellis NA. Peterlongo P, et al. Among authors: nafa k. Int J Cancer. 2005 Apr 10;114(3):505-7. doi: 10.1002/ijc.20767. Int J Cancer. 2005. PMID: 15578699 No abstract available.

9

TGFBR1*6A may contribute to hereditary colorectal cancer.

Bian Y, Caldes T, Wijnen J, Franken P, Vasen H, Kaklamani V, Nafa K, Peterlongo P, Ellis N, Baron JA, Burn J, Moeslein G, Morrison PJ, Chen Y, Ahsan H, Watson P, Lynch HT, de la Chapelle A, Fodde R, Pasche B. Bian Y, et al. Among authors: nafa k. J Clin Oncol. 2005 May 1;23(13):3074-8. doi: 10.1200/JCO.2005.00.281. J Clin Oncol. 2005. PMID: 15860866

10

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.

Shaag A, Walsh T, Renbaum P, Kirchhoff T, Nafa K, Shiovitz S, Mandell JB, Welcsh P, Lee MK, Ellis N, Offit K, Levy-Lahad E, King MC. Shaag A, et al. Among authors: nafa k. Hum Mol Genet. 2005 Feb 15;14(4):555-63. doi: 10.1093/hmg/ddi052. Epub 2005 Jan 13. Hum Mol Genet. 2005. PMID: 15649950

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