Williams C - Search Results

1

Antibody Validation for Estrogen Receptor Beta.

Birgersson M, Katona B, Lindskog C, Pontén F, Williams C. Birgersson M, et al. Among authors: williams c. Methods Mol Biol. 2022;2418:1-23. doi: 10.1007/978-1-0716-1920-9_1. Methods Mol Biol. 2022. PMID: 35119656

2

Genomic analysis of single cells from human basal cell cancer using laser-assisted capture microscopy.

Pontén F, Williams C, Ling G, Ahmadian A, Nistér M, Lundeberg J, Pontén J, Uhlén M. Pontén F, et al. Among authors: williams c. Mutat Res. 1997 Sep;382(1-2):45-55. doi: 10.1016/s1383-5726(97)00008-3. Mutat Res. 1997. PMID: 9360637

3

Assessment of sequence-based p53 gene analysis in human breast cancer: messenger RNA in comparison with genomic DNA targets.

Williams C, Norberg T, Ahmadian A, Pontén F, Bergh J, Inganäs M, Lundeberg J, Uhlén M. Williams C, et al. Clin Chem. 1998 Mar;44(3):455-62. Clin Chem. 1998. PMID: 9510848

4

Cloning and characterization of ZNF189, a novel human Krüppel-like zinc finger gene localized to chromosome 9q22-q31.

Odeberg J, Røsok O, Gudmundsson GH, Ahmadian A, Roshani L, Williams C, Larsson C, Pontén F, Uhlén M, Asheim HC, Lundeberg J. Odeberg J, et al. Among authors: williams c. Genomics. 1998 Jun 1;50(2):213-21. doi: 10.1006/geno.1998.5309. Genomics. 1998. PMID: 9653648

5

Genetic instability in the 9q22.3 region is a late event in the development of squamous cell carcinoma.

Ahmadian A, Ren ZP, Williams C, Pontén F, Odeberg J, Pontén J, Uhlén M, Lundeberg J. Ahmadian A, et al. Among authors: williams c. Oncogene. 1998 Oct 8;17(14):1837-43. doi: 10.1038/sj.onc.1202080. Oncogene. 1998. PMID: 9778050

6

Context-dependent Taq-polymerase-mediated nucleotide alterations, as revealed by direct sequencing of the ZNF189 gene: implications for mutation detection.

Odeberg J, Ahmadian A, Williams C, Uhlén M, Pontén F, Lundeberg J. Odeberg J, et al. Among authors: williams c. Gene. 1999 Jul 22;235(1-2):103-9. doi: 10.1016/s0378-1119(99)00205-x. Gene. 1999. PMID: 10415338

7

A high frequency of sequence alterations is due to formalin fixation of archival specimens.

Williams C, Pontén F, Moberg C, Söderkvist P, Uhlén M, Pontén J, Sitbon G, Lundeberg J. Williams C, et al. Am J Pathol. 1999 Nov;155(5):1467-71. doi: 10.1016/S0002-9440(10)65461-2. Am J Pathol. 1999. PMID: 10550302 Free PMC article.

8

Analysis of p53 mutations in single cells obtained from histological tissue sections.

Persson AE, Ling G, Williams C, Bäckvall H, Pontén J, Pontén F, Lundeberg J. Persson AE, et al. Among authors: williams c. Anal Biochem. 2000 Dec 1;287(1):25-31. doi: 10.1006/abio.2000.4830. Anal Biochem. 2000. PMID: 11078579

9

PATCHED and p53 gene alterations in sporadic and hereditary basal cell cancer.

Ling G, Ahmadian A, Persson A, Undén AB, Afink G, Williams C, Uhlén M, Toftgård R, Lundeberg J, Pontén F. Ling G, et al. Among authors: williams c. Oncogene. 2001 Nov 22;20(53):7770-8. doi: 10.1038/sj.onc.1204946. Oncogene. 2001. PMID: 11753655

10

The mutagenic effect of ultraviolet-A1 on human skin demonstrated by sequencing the p53 gene in single keratinocytes.

Persson AE, Edström DW, Bäckvall H, Lundeberg J, Pontén F, Ros AM, Williams C. Persson AE, et al. Among authors: williams c. Photodermatol Photoimmunol Photomed. 2002 Dec;18(6):287-93. doi: 10.1034/j.1600-0781.2002.02781.x. Photodermatol Photoimmunol Photomed. 2002. PMID: 12535024

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