Zander C - Search Results

1

CAG repeat sequences in bipolar affective disorder: no evidence for association in a French population.

Zander C, Schürhoff F, Laurent C, Chavand O, Bellivier F, Samolyk D, Leboyer M, Allilaire JF, Cann H, Néri C, Mallet J. Zander C, et al. Am J Med Genet. 1998 Jul 10;81(4):338-41. Am J Med Genet. 1998. PMID: 9674981

2

Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases.

Laurent C, Zander C, Thibaut F, Bonnet-Brilhault F, Chavand O, Jay M, Samolyk D, Petit M, Martinez M, Campion D, Néri C, Mallet J, Cann H. Laurent C, et al. Among authors: zander c. Am J Med Genet. 1998 Jul 10;81(4):342-6. doi: 10.1002/(sici)1096-8628(19980710)81:4<342::aid-ajmg12>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9674982

3

No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24.

Zander C, Yuan QP, Lindblad K, Stevanin G, Dürr A, Davoine CS, Hazan J, Fontaine B, Brice A, Schalling M. Zander C, et al. Neurosci Lett. 2000 Jan 21;279(1):41-4. doi: 10.1016/s0304-3940(99)00946-5. Neurosci Lett. 2000. PMID: 10670783

4

Expanded trinucleotide CAG repeats in families with bipolar affective disorder.

Mendlewicz J, Lindbald K, Souery D, Mahieu B, Nylander PO, De Bruyn A, Zander C, Engström C, Adolfsson R, Van Broeckhoven C, Schalling M, Lipp O. Mendlewicz J, et al. Among authors: zander c. Biol Psychiatry. 1997 Dec 15;42(12):1115-22. doi: 10.1016/s0006-3223(97)00395-8. Biol Psychiatry. 1997. PMID: 9426881 Clinical Trial.

5

Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method.

Lindblad K, Nylander PO, De bruyn A, Sourey D, Zander C, Engström C, Holmgren G, Hudson T, Chotai J, Mendlewicz J, et al. Lindblad K, et al. Among authors: zander c. Neurobiol Dis. 1995 Feb;2(1):55-62. doi: 10.1006/nbdi.1995.0006. Neurobiol Dis. 1995. PMID: 8980009 Clinical Trial.

6

Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders?

Lindblad K, Nylander PO, Zander C, Yuan QP, Ståhle L, Engström C, Balciuniene J, Pettersson U, Breschel T, McInnis M, Ross CA, Adolfsson R, Schalling M. Lindblad K, et al. Among authors: zander c. Mol Psychiatry. 1998 Sep;3(5):405-10. doi: 10.1038/sj.mp.4000416. Mol Psychiatry. 1998. PMID: 9774773

7

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A. Fujigasaki H, et al. Among authors: zander c. Ann Neurol. 2001 Jan;49(1):117-21. Ann Neurol. 2001. PMID: 11198281

8

Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions.

Lebre AS, Jamot L, Takahashi J, Spassky N, Leprince C, Ravisé N, Zander C, Fujigasaki H, Kussel-Andermann P, Duyckaerts C, Camonis JH, Brice A. Lebre AS, et al. Among authors: zander c. Hum Mol Genet. 2001 May 15;10(11):1201-13. doi: 10.1093/hmg/10.11.1201. Hum Mol Genet. 2001. PMID: 11371513

9

An expanded CAG repeat sequence in spinocerebellar ataxia type 7.

Lindblad K, Savontaus ML, Stevanin G, Holmberg M, Digre K, Zander C, Ehrsson H, David G, Benomar A, Nikoskelainen E, Trottier Y, Holmgren G, Ptacek LJ, Anttinen A, Brice A, Schalling M. Lindblad K, et al. Among authors: zander c. Genome Res. 1996 Oct;6(10):965-71. doi: 10.1101/gr.6.10.965. Genome Res. 1996. PMID: 8908515 Free article.

10

Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred.

Teh BT, Sullivan AA, Farnebo F, Zander C, Li FY, Strachan N, Schalling M, Larsson C, Sandstrom P. Teh BT, et al. Among authors: zander c. Clin Genet. 1997 Jan;51(1):52-5. doi: 10.1111/j.1399-0004.1997.tb02415.x. Clin Genet. 1997. PMID: 9084936

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