Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

443 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer.
Lindblom A, Tannergård P, Werelius B, Nordenskjöld M. Lindblom A, et al. Nat Genet. 1993 Nov;5(3):279-82. doi: 10.1038/ng1193-279. Nat Genet. 1993. PMID: 7903889
The APC gene on chromosome 5 causing adenomatous polyposis coli represents a minority of the inherited colon cancer cases, while hereditary-non polyposis colon cancer (HNPCC) may cause five percent of all human colon cancer. ...We now present tight linkage between a
The APC gene on chromosome 5 causing adenomatous polyposis coli represents a minority of the inherited colon cancer cases, while here …
[Families with hereditary cancer--a target group for prevention].
Lindblom A, Nordenskjöld M. Lindblom A, et al. Lakartidningen. 1990 Nov 7;87(45):3775-8. Lakartidningen. 1990. PMID: 2233058 Swedish.
Although a large proportion of the population contract cancer, the risk is not uniform. In a small group (an estimated five per cent) with hereditary predisposition, the risk of cancer is high (often as high as 50 per cent) in every child of an affected parent. Anot …
Although a large proportion of the population contract cancer, the risk is not uniform. In a small group (an estimated five pe …
Finnish mutations in Swedish HNPCC families.
Tannergård P, Nordenskjöld M, Lindblom A. Tannergård P, et al. Among authors: lindblom a. Nat Med. 1995 Nov;1(11):1104. doi: 10.1038/nm1195-1104b. Nat Med. 1995. PMID: 7584969 No abstract available.
Sequence variability of a prolonged tetranucleotide repeat.
Liu Y, Rasool O, Grandér D, Lindblom A, Einhorn S. Liu Y, et al. Among authors: lindblom a. Hum Mol Genet. 1995 Apr;4(4):727-9. doi: 10.1093/hmg/4.4.727. Hum Mol Genet. 1995. PMID: 7633423
A tetranucleotide repeat located in intron 20 of the RB gene consists of 16-26 CTTT(+/- T) repeats in 99% of the alleles. In the remaining 1% of alleles the segment is extended to a length of > 60 repeats. ...
A tetranucleotide repeat located in intron 20 of the RB gene consists of 16-26 CTTT(+/- T) repeats in 99% of the alleles. In the rema
Familial breast cancer and genes involved in breast carcinogenesis.
Lindblom A. Lindblom A. Breast Cancer Res Treat. 1995 May;34(2):171-83. doi: 10.1007/BF00665789. Breast Cancer Res Treat. 1995. PMID: 7647334 Review.
Breast cancer has often been reported to run in families, and the most important risk factor for the disease is a family history of breast cancer. ...Such cases may be characterized by early onset, bilateral disease, prolonged survival, and anticipation, mainly seen as …
Breast cancer has often been reported to run in families, and the most important risk factor for the disease is a family history of b …
High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium.
Cornelis RS, Neuhausen SL, Johansson O, Arason A, Kelsell D, Ponder BA, Tonin P, Hamann U, Lindblom A, Lalle P, et al. Cornelis RS, et al. Among authors: lindblom a. Genes Chromosomes Cancer. 1995 Jul;13(3):203-10. doi: 10.1002/gcc.2870130310. Genes Chromosomes Cancer. 1995. PMID: 7669740
Tumor genotypes were determined at at least 2 constitutionally heterozygous markers flanking BRCAl in a total of 58 tumors from these families. ...These results strongly suggest that BRCAl is a tumor suppressor gene and that LOH is greatly favored to fully inactivat …
Tumor genotypes were determined at at least 2 constitutionally heterozygous markers flanking BRCAl in a total of 58 tumors from these …
[Experiences from a clinic for patients with hereditary cancer. Diagnosis of genetic carriers may prevent cancer].
Lindblom A, Iselius L. Lindblom A, et al. Lakartidningen. 1995 May 3;92(18):1915-8. Lakartidningen. 1995. PMID: 7746044 Swedish. No abstract available.
[The first breast cancer gene isolated. Safer risk assessment for affected families].
Iselius L, Larsson C, Lindblom A, Sandelin K, Wickman M, Wilking N. Iselius L, et al. Among authors: lindblom a. Lakartidningen. 1995 Jan 25;92(4):269-73, 275. Lakartidningen. 1995. PMID: 7845095 Swedish. No abstract available.
Genetic rearrangements in sporadic and familial gastric carcinomas detected with microsatellite markers.
Zelada-Hedman M, Iselius L, Gunvén P, Weger A, Nordenskjöld M, Skoog L, Lindblom A. Zelada-Hedman M, et al. Among authors: lindblom a. Eur J Surg Oncol. 1994 Dec;20(6):667-73. Eur J Surg Oncol. 1994. PMID: 7995419
Four patients had a family history of gastro-intestinal cancer, and six tumours were considered sporadic. We also studied a new mechanism in tumourigenesis recently reported in hereditary non polyposis colon cancer, a defect in mismatch repair that is seen as …
Four patients had a family history of gastro-intestinal cancer, and six tumours were considered sporadic. We also studied a ne …
Sublocalization of a locus at 3p21.3-23 predisposing to hereditary nonpolyposis colon cancer.
Tannergård P, Zabarovsky E, Stanbridge E, Nordenskjöld M, Lindblom A. Tannergård P, et al. Among authors: lindblom a. Hum Genet. 1994 Aug;94(2):210-4. doi: 10.1007/BF00202874. Hum Genet. 1994. PMID: 8045572
Hereditary nonpolyposis colon cancer (HNPCC) is a heterogeneous disease caused by at least three different genes on chromosomes 2 and 3, and one or more additional chromosomes. We used 19 dinucleotide markers in order to sublocalize further the 3p locus linked to HNPCC, an …
Hereditary nonpolyposis colon cancer (HNPCC) is a heterogeneous disease caused by at least three different genes on chromosomes 2 and …
443 results
Jump to page
Feedback