Farnebo F - Search Results

1

Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping.

Nordgren A, Farnebo F, Johansson B, Holmgren G, Forestier E, Larsson C, Söderhäll S, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: farnebo f. Eur J Haematol. 2001 May;66(5):297-304. doi: 10.1034/j.1600-0609.2001.066005297.x. Eur J Haematol. 2001. PMID: 11422408

2

Chromosomal alterations in 15 breast cancer cell lines by comparative genomic hybridization and spectral karyotyping.

Kytölä S, Rummukainen J, Nordgren A, Karhu R, Farnebo F, Isola J, Larsson C. Kytölä S, et al. Among authors: farnebo f. Genes Chromosomes Cancer. 2000 Jul;28(3):308-17. doi: 10.1002/1098-2264(200007)28:3<308::aid-gcc9>3.0.co;2-b. Genes Chromosomes Cancer. 2000. PMID: 10862037

3

Detailed characterization of a complex karyotype in a patient with primary plasma cell leukaemia using multicolour spectral karyotyping and micro-FISH.

Nordgren A, Farnebo F, Björkholm M, Sahlén S, Porwit-MacDonald A, Osby E, Kytölä S, Larsson C, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: farnebo f. Hematol J. 2000;1(2):95-101. doi: 10.1038/sj.thj.6200011. Hematol J. 2000. PMID: 11920176

4

Characterization of chromosomal abnormalities in prostate cancer cell lines by spectral karyotyping.

Pan Y, Kytölä S, Farnebo F, Wang N, Lui WO, Nupponen N, Isola J, Visakorpi T, Bergerheim US, Larsson C. Pan Y, et al. Among authors: farnebo f. Cytogenet Cell Genet. 1999;87(3-4):225-32. doi: 10.1159/000015432. Cytogenet Cell Genet. 1999. PMID: 10702678

5

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism.

Farnebo F, Teh BT, Dotzenrath C, Wassif WS, Svensson A, White I, Betz R, Goretzki P, Sandelin K, Farnebo LO, Larsson C. Farnebo F, et al. Among authors: farnebo lo. Hum Genet. 1997 Mar;99(3):342-9. doi: 10.1007/s004390050369. Hum Genet. 1997. PMID: 9050920

6

Allelic loss on chromosome 11 is uncommon in parathyroid glands of patients with hypercalcaemic secondary hyperparathyroidism.

Farnebo F, Farnebo LO, Nordenström J, Larsson C. Farnebo F, et al. Among authors: farnebo lo. Eur J Surg. 1997 May;163(5):331-7. Eur J Surg. 1997. PMID: 9195165

7

Aberrations of chromosome 8 in 16 breast cancer cell lines by comparative genomic hybridization, fluorescence in situ hybridization, and spectral karyotyping.

Rummukainen J, Kytölä S, Karhu R, Farnebo F, Larsson C, Isola JJ. Rummukainen J, et al. Among authors: farnebo f. Cancer Genet Cytogenet. 2001 Apr 1;126(1):1-7. doi: 10.1016/s0165-4608(00)00387-3. Cancer Genet Cytogenet. 2001. PMID: 11343771

8

Homozygous inactivation of the MEN1 gene as a specific somatic event in a case of secondary hyperparathyroidism.

Forsberg L, Villablanca A, Välimäki S, Farnebo F, Farnebo LO, Lagercrantz S, Larsson C. Forsberg L, et al. Among authors: farnebo f, farnebo lo. Eur J Endocrinol. 2001 Oct;145(4):415-20. doi: 10.1530/eje.0.1450415. Eur J Endocrinol. 2001. PMID: 11580998

9

Patterns of chromosomal imbalances in parathyroid carcinomas.

Kytölä S, Farnebo F, Obara T, Isola J, Grimelius L, Farnebo LO, Sandelin K, Larsson C. Kytölä S, et al. Among authors: farnebo f, farnebo lo. Am J Pathol. 2000 Aug;157(2):579-86. doi: 10.1016/S0002-9440(10)64568-3. Am J Pathol. 2000. PMID: 10934160 Free PMC article.

10

Mapping of the human Ca2+ channel beta 4 subunit to 2q22-23 and its expression in developing mouse.

Betz R, Leibiger B, Farnebo F, Lagercrantz S, Piehl F, Leibiger I, Larsson C. Betz R, et al. Among authors: farnebo f. Mamm Genome. 1998 Apr;9(4):310-1. doi: 10.1007/s003359900755. Mamm Genome. 1998. PMID: 9530629 No abstract available.

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