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Items: 4

1.

Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosa.

Koronyo-Hamaoui M, Frisch A, Stein D, Denziger Y, Leor S, Michaelovsky E, Laufer N, Carel C, Fennig S, Mimouni M, Ram A, Zubery E, Jeczmien P, Apter A, Weizman A, Gak E.

J Psychiatr Res. 2007 Jan-Feb;41(1-2):160-7. Epub 2005 Sep 12.

PMID:
16157352
2.

CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population.

Koronyo-Hamaoui M, Gak E, Stein D, Frisch A, Danziger Y, Leor S, Michaelovsky E, Laufer N, Carel C, Fennig S, Mimouni M, Apter A, Goldman B, Barkai G, Weizman A.

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):76-80.

PMID:
15389773
3.

Novel truncated isoform of SK3 potassium channel is a potent dominant-negative regulator of SK currents: implications in schizophrenia.

Tomita H, Shakkottai VG, Gutman GA, Sun G, Bunney WE, Cahalan MD, Chandy KG, Gargus JJ.

Mol Psychiatry. 2003 May;8(5):524-35, 460. Erratum in: Mol Psychiatry. 2003 Aug;8(8):766.

PMID:
12808432
4.

Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study.

Koronyo-Hamaoui M, Danziger Y, Frisch A, Stein D, Leor S, Laufer N, Carel C, Fennig S, Minoumi M, Apter A, Goldman B, Barkai G, Weizman A, Gak E.

Mol Psychiatry. 2002;7(1):82-5.

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