Baylin SB - Search Results

1

RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer.

Blaugrund JE, Johns MM Jr, Eby YJ, Ball DW, Baylin SB, Hruban RH, Sidransky D. Blaugrund JE, et al. Among authors: baylin sb. Hum Mol Genet. 1994 Oct;3(10):1895-7. doi: 10.1093/hmg/3.10.1895. Hum Mol Genet. 1994. PMID: 7849720 No abstract available.

2

Human calcitonin gene regulation by helix-loop-helix recognition sequences.

Ball DW, Compton D, Nelkin BD, Baylin SB, de Bustros A. Ball DW, et al. Among authors: baylin sb. Nucleic Acids Res. 1992 Jan 11;20(1):117-23. doi: 10.1093/nar/20.1.117. Nucleic Acids Res. 1992. PMID: 1738589 Free PMC article.

3

Transcription factor levels in medullary thyroid carcinoma cells differentiated by Harvey ras oncogene: c-jun is increased.

Nelkin BD, Borges M, Mabry M, Baylin SB. Nelkin BD, et al. Among authors: baylin sb. Biochem Biophys Res Commun. 1990 Jul 16;170(1):140-6. doi: 10.1016/0006-291x(90)91251-m. Biochem Biophys Res Commun. 1990. PMID: 2115330 Free article.

4

Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma.

Nelkin BD, Nakamura Y, White RW, de Bustros AC, Herman J, Wells SA Jr, Baylin SB. Nelkin BD, et al. Among authors: baylin sb. Cancer Res. 1989 Aug 1;49(15):4114-9. Cancer Res. 1989. PMID: 2568166

5

Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers.

Herman JG, Merlo A, Mao L, Lapidus RG, Issa JP, Davidson NE, Sidransky D, Baylin SB. Herman JG, et al. Among authors: baylin sb. Cancer Res. 1995 Oct 15;55(20):4525-30. Cancer Res. 1995. PMID: 7553621

6

5' CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers.

Merlo A, Herman JG, Mao L, Lee DJ, Gabrielson E, Burger PC, Baylin SB, Sidransky D. Merlo A, et al. Among authors: baylin sb. Nat Med. 1995 Jul;1(7):686-92. doi: 10.1038/nm0795-686. Nat Med. 1995. PMID: 7585152

7

Molecular abnormalities in tumors associated with multiple endocrine neoplasia type 2.

Nelkin BD, Ball DW, Baylin SB. Nelkin BD, et al. Among authors: baylin sb. Endocrinol Metab Clin North Am. 1994 Mar;23(1):187-213. Endocrinol Metab Clin North Am. 1994. PMID: 7913025 Review.

8

Management of pheochromocytomas in patients with multiple endocrine neoplasia type 2 syndromes.

Lairmore TC, Ball DW, Baylin SB, Wells SA Jr. Lairmore TC, et al. Among authors: baylin sb. Ann Surg. 1993 Jun;217(6):595-601; discussion 601-3. doi: 10.1097/00000658-199306000-00001. Ann Surg. 1993. PMID: 8099474 Free PMC article.

9

Homozygous deletion on chromosome 9p and loss of heterozygosity on 9q, 6p, and 6q in primary human small cell lung cancer.

Merlo A, Gabrielson E, Mabry M, Vollmer R, Baylin SB, Sidransky D. Merlo A, et al. Among authors: baylin sb. Cancer Res. 1994 May 1;54(9):2322-6. Cancer Res. 1994. PMID: 8162574

10

Frequent microsatellite instability in primary small cell lung cancer.

Merlo A, Mabry M, Gabrielson E, Vollmer R, Baylin SB, Sidransky D. Merlo A, et al. Among authors: baylin sb. Cancer Res. 1994 Apr 15;54(8):2098-101. Cancer Res. 1994. PMID: 8174113

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

580 results

Search Page

Filters