Holmberg M - Search Results

1

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.

Jonasson J, Juvonen V, Sistonen P, Ignatius J, Johansson D, Björck EJ, Wahlström J, Melberg A, Holmgren G, Forsgren L, Holmberg M. Jonasson J, et al. Among authors: holmberg m. Eur J Hum Genet. 2000 Dec;8(12):918-22. doi: 10.1038/sj.ejhg.5200557. Eur J Hum Genet. 2000. PMID: 11175279

2

Cloning and expression analysis of the murine homolog of the spinocerebellar ataxia type 7 (SCA7) gene.

Ström AL, Jonasson J, Hart P, Brännström T, Forsgren L, Holmberg M. Ström AL, et al. Among authors: holmberg m. Gene. 2002 Feb 20;285(1-2):91-9. doi: 10.1016/s0378-1119(02)00399-2. Gene. 2002. PMID: 12039035

3

Expression of ataxin-7 in CNS and non-CNS tissue of normal and SCA7 individuals.

Jonasson J, Ström AL, Hart P, Brännström T, Forsgren L, Holmberg M. Jonasson J, et al. Among authors: holmberg m. Acta Neuropathol. 2002 Jul;104(1):29-37. doi: 10.1007/s00401-001-0514-4. Epub 2002 Mar 2. Acta Neuropathol. 2002. PMID: 12070661

4

Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.

Johansson J, Forsgren L, Sandgren O, Brice A, Holmgren G, Holmberg M. Johansson J, et al. Among authors: holmberg m. Hum Mol Genet. 1998 Feb;7(2):171-6. doi: 10.1093/hmg/7.2.171. Hum Mol Genet. 1998. PMID: 9425223

5

A role for both wild-type and expanded ataxin-7 in transcriptional regulation.

Ström AL, Forsgren L, Holmberg M. Ström AL, et al. Among authors: holmberg m. Neurobiol Dis. 2005 Dec;20(3):646-55. doi: 10.1016/j.nbd.2005.04.018. Epub 2005 Jun 3. Neurobiol Dis. 2005. PMID: 15936949

6

Identification and characterization of Spinocerebellar Ataxia Type 7 (SCA7) isoform SCA7b in mice.

Ström AL, Forsgren L, Holmberg M. Ström AL, et al. Among authors: holmberg m. Biochim Biophys Acta. 2005 Dec 20;1731(3):149-53. doi: 10.1016/j.bbaexp.2005.10.004. Epub 2005 Nov 2. Biochim Biophys Acta. 2005. PMID: 16297465

7

The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease.

Einarsdottir E, Söderström I, Löfgren-Burström A, Haraldsson S, Nilsson-Ardnor S, Penha-Goncalves C, Lind L, Holmgren G, Holmberg M, Asplund K, Holmberg D. Einarsdottir E, et al. Among authors: holmberg d, holmberg m. Eur J Hum Genet. 2003 Jan;11(1):81-4. doi: 10.1038/sj.ejhg.5200903. Eur J Hum Genet. 2003. PMID: 12529710

8

Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.

Holmberg M, Johansson J, Forsgren L, Heijbel J, Sandgren O, Holmgren G. Holmberg M, et al. Hum Mol Genet. 1995 Aug;4(8):1441-5. doi: 10.1093/hmg/4.8.1441. Hum Mol Genet. 1995. PMID: 7581386

9

[Growing genes cause neurological diseases].

Johansson J, Holmgren G, Forsgren L, Holmberg M. Johansson J, et al. Among authors: holmberg m. Lakartidningen. 1999 Feb 24;96(8):897-900. Lakartidningen. 1999. PMID: 10089735 Review. Swedish.

10

Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study.

Drugge U, Holmberg M, Holmgren G, Almay BG, Linderholm H. Drugge U, et al. Among authors: holmberg m. J Med Genet. 1995 May;32(5):344-7. doi: 10.1136/jmg.32.5.344. J Med Genet. 1995. PMID: 7616539 Free PMC article.

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