Noll WW - Search Results

1

Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests.

Xue F, Yu H, Maurer LH, Memoli VA, Nutile-McMenemy N, Schuster MK, Bowden DW, Mao J, Noll WW. Xue F, et al. Among authors: noll ww. Hum Mol Genet. 1994 Apr;3(4):635-8. doi: 10.1093/hmg/3.4.635. Hum Mol Genet. 1994. PMID: 7915165

2

Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products.

Moir DT, Dorman TE, Xue F, Ma NS, Stanton VP Jr, Housman D, Bowden DW, Noll WW, Mao J. Moir DT, et al. Among authors: noll ww. Gene. 1993 Dec 22;136(1-2):177-83. doi: 10.1016/0378-1119(93)90461-b. Gene. 1993. PMID: 7904972

3

A genetic linkage map of 32 loci on human chromosome 10.

Bowden DW, Gravius TC, Green P, Falls K, Wurster-Hill D, Noll W, Müller-Kahle H, Donis-Keller H. Bowden DW, et al. Genomics. 1989 Nov;5(4):718-26. doi: 10.1016/0888-7543(89)90113-4. Genomics. 1989. PMID: 2574142

4

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

Eng C, Clayton D, Schuffenecker I, Lenoir G, Cote G, Gagel RF, van Amstel HK, Lips CJ, Nishisho I, Takai SI, Marsh DJ, Robinson BG, Frank-Raue K, Raue F, Xue F, Noll WW, Romei C, Pacini F, Fink M, Niederle B, Zedenius J, Nordenskjöld M, Komminoth P, Hendy GN, Mulligan LM, et al. Eng C, et al. Among authors: noll ww. JAMA. 1996 Nov 20;276(19):1575-9. JAMA. 1996. PMID: 8918855

5

Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma.

Kinlaw WB, Scott SM, Maue RA, Memoli VA, Harris RD, Daniels GH, Porter DM, Belloni DR, Spooner ET, Ernesti MM, Noll WW. Kinlaw WB, et al. Among authors: noll ww. Clin Endocrinol (Oxf). 2005 Dec;63(6):676-82. doi: 10.1111/j.1365-2265.2005.02400.x. Clin Endocrinol (Oxf). 2005. PMID: 16343103

6

Characterization of radiation/fusion hybrids containing parts of human chromosome 10 and their use in mapping chromosome 10-specific probes.

Rothschild CB, Noll WW, Gravius TC, Schuster MK, Nutile-McMenemy N, Jones C, Bowden DW. Rothschild CB, et al. Among authors: noll ww. Genomics. 1992 May;13(1):25-34. doi: 10.1016/0888-7543(92)90197-z. Genomics. 1992. PMID: 1349579

7

Localization of acyl coenzyme A:cholesterol acyltransferase gene to human chromosome 1q25.

Chang CC, Noll WW, Nutile-McMenemy N, Lindsay EA, Baldini A, Chang W, Chang TY. Chang CC, et al. Among authors: noll ww. Somat Cell Mol Genet. 1994 Jan;20(1):71-4. doi: 10.1007/BF02257489. Somat Cell Mol Genet. 1994. PMID: 8197480

8

Familial medullary carcinoma of the thyroid: clinical studies in northern New England.

Noll WW, Maurer LH, Herzberg VL, Beisswenger PJ, Quinn BM, Cate CC, Bassick JP, Clark PA, Colacchio TA. Noll WW, et al. Henry Ford Hosp Med J. 1984;32(4):244-5. Henry Ford Hosp Med J. 1984. PMID: 6152459 Free article. No abstract available.

9

Isolation and growth characteristics of continuous cell lines from small-cell carcinoma of the lung.

Pettengill OS, Sorenson GD, Wurster-Hill DH, Curphey TJ, Noll WW, Cate CC, Maurer LH. Pettengill OS, et al. Among authors: noll ww. Cancer. 1980 Mar 1;45(5):906-18. doi: 10.1002/1097-0142(19800301)45:5<906::aid-cncr2820450513>3.0.co;2-h. Cancer. 1980. PMID: 6266631

10

Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma.

Siegelman M, Mohabeer A, Fahey TJ 3rd, Tomlinson G, Mayambala C, Jafari S, Noll WW, Thibodeau SN, Dawson DB. Siegelman M, et al. Among authors: noll ww. Clin Chem. 1997 Mar;43(3):453-7. Clin Chem. 1997. PMID: 9068588

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