Hammarström L - Search Results

1

The ATM gene and susceptibility to breast cancer: analysis of 38 breast tumors reveals no evidence for mutation.

Vorechovský I, Rasio D, Luo L, Monaco C, Hammarström L, Webster AD, Zaloudik J, Barbanti-Brodani G, James M, Russo G, et al. Vorechovský I, et al. Among authors: hammarstrom l. Cancer Res. 1996 Jun 15;56(12):2726-32. Cancer Res. 1996. PMID: 8665503

2

ATM mutations in cancer families.

Vorechovský I, Luo L, Lindblom A, Negrini M, Webster AD, Croce CM, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. Cancer Res. 1996 Sep 15;56(18):4130-3. Cancer Res. 1996. PMID: 8797579

3

Exon-scanning mutation analysis of the ATM gene in patients with ataxia-telangiectasia.

Vorechovský I, Luo L, Prudente S, Chessa L, Russo G, Kanariou M, James M, Negrini M, Webster AD, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. Eur J Hum Genet. 1996;4(6):352-5. doi: 10.1159/000472231. Eur J Hum Genet. 1996. PMID: 9043869

4

Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia.

Vorechovský I, Luo L, Dyer MJ, Catovsky D, Amlot PL, Yaxley JC, Foroni L, Hammarström L, Webster AD, Yuille MA. Vorechovský I, et al. Among authors: hammarstrom l. Nat Genet. 1997 Sep;17(1):96-9. doi: 10.1038/ng0997-96. Nat Genet. 1997. PMID: 9288106

5

Ataxia-telangiectasia and T-cell leukemias: no evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLL.

Luo L, Lu FM, Hart S, Foroni L, Rabbani H, Hammarström L, Yuille MR, Catovsky D, Webster AD, Vorechovský I. Luo L, et al. Among authors: hammarstrom l. Cancer Res. 1998 Jun 1;58(11):2293-7. Cancer Res. 1998. PMID: 9622061

6

The PAX5 gene: a linkage and mutation analysis in candidate human primary immunodeficiencies.

Vorechovský I, Koskinen S, Paganelli R, Smith CI, Busslinger M, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. Immunogenetics. 1995;42(2):149-52. doi: 10.1007/BF00178590. Immunogenetics. 1995. PMID: 7607706 No abstract available.

7

DNA-based mutation analysis of Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinaemia.

Vorechovský I, Vihinen M, de Saint Basile G, Honsová S, Hammarström L, Müller S, Nilsson L, Fischer A, Smith CI. Vorechovský I, et al. Among authors: hammarstrom l. Hum Mol Genet. 1995 Jan;4(1):51-8. doi: 10.1093/hmg/4.1.51. Hum Mol Genet. 1995. PMID: 7711734

8

Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia.

Vorechovský I, Luo L, Hertz JM, Frøland SS, Klemola T, Fiorini M, Quinti I, Paganelli R, Ozsahin H, Hammarström L, Webster AD, Smith CI. Vorechovský I, et al. Among authors: hammarstrom l. Hum Mutat. 1997;9(5):418-25. doi: 10.1002/(SICI)1098-1004(1997)9:5<418::AID-HUMU7>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9143921

9

Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition.

Vorechovský I, Webster AD, Plebani A, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. Am J Hum Genet. 1999 Apr;64(4):1096-109. doi: 10.1086/302326. Am J Hum Genet. 1999. PMID: 10090895 Free PMC article.

10

A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: evidence from meiotic mapping of 83 multiple-case families.

Vorechovský I, Blennow E, Nordenskjöld M, Webster AD, Hammarström L. Vorechovský I, et al. Among authors: hammarstrom l. J Immunol. 1999 Aug 15;163(4):2236-42. J Immunol. 1999. PMID: 10438966

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