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The Journal of Investigative Dermatology|October 31, 2002
A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichiaIzabella Klein, Reuven Bergman, Margerita Indelman, et al.
Neuroreport|September 18, 2008
Hypothalamic-pituitary-adrenal axis disregulation in PrPC-null miceManuel Sanchez-Alavez, José R Criado, Izabella Klein, et al.
Haematologica|July 15, 2003
Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia AHajnalka Andrikovics, Izabella Klein, András Bors, et al.
Genetic Testing and Molecular Biomarkers|September 22, 2010
Frequencies of four ATP-binding cassette transporter G8 polymorphisms in patients with ischemic vascular diseasesAnikó Szilvási, Hajnalka Andrikovics, Endre Pongrácz, et al.
Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet Lapja = Official Journal of the Hungarian Association of Psychopharmacology|March 6, 2017
[An attempt to identify 22q11.2 microdeletions in samples of the Hungarian schizophrenia DNA bank by multiplex ligation-based probe amplification (MLPA): literature review, methodology and results]Izabella Klein, Katalin Szocs, Katalin Vincze, et al.
FEBS Letters|October 24, 2006
Co-expression of human ABCG5 and ABCG8 in insect cells generates an androstan stimulated membrane ATPase activityMarianna Müller, Izabella Klein, Szilárd Kopácsi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2007
Night eating and obesity in the EP3R-deficient mouseManuel Sanchez-Alavez, Izabella Klein, Sara E Brownell, et al.
European Archives of Psychiatry and Clinical Neuroscience|November 18, 2023
Differential neurocognitive profiles in adult attention-deficit/hyperactivity disorder subtypes revealed by the Cambridge Neuropsychological Test Automated BatterySzilvia Somogyi, Tünde Kilencz, Katalin Szőcs, et al.
Biochemical and Biophysical Research Communications|July 9, 2004
Functional expression and characterization of the human ABCG1 and ABCG4 proteins: indications for heterodimerizationJudit Cserepes, Zsófia Szentpétery, László Seres, et al.
Wiener Klinische Wochenschrift|July 26, 2006
Genotype-phenotype correlations in Hungarian patients with hereditary medullary thyroid cancerAttila Patocs, Izabella Klein, Aniko Szilvasi, et al.
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