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Precise switching of DNA replication timing in the GC content transition area in the human major histocompatibility complexMOLECULAR AND CELLULAR BIOLOGYIF2.72023-03-2993OAAI
CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model miceNEUROBIOLOGY OF DISEASEIF5.62020-07-0179OAAI
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Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in miceCOMMUNICATIONS BIOLOGYIF5.12018-07-1974OAAI
Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndromeHUMAN MOLECULAR GENETICSIF3.22013-08-06146OAAI
A homozygous mutation of voltage-gated sodium channel βI gene SCN1B in a patient with Dravet syndromeEPILEPSIAIF6.62012-11-1382OA
Immunoliposome-based, non-viral gene delivery in a knock-out mouse model of Lafora inclusion body diseaseMOLECULAR GENETICS AND METABOLISMIF3.52009-02-010PREAI
Comparative sequencing of human and chimpanzee MHC class I regions unveils insertions/deletions as the major path to genomic divergencePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAIF9.12003-06-10133OAAI
Characterization and chromosomal distribution of a novel satellite DNA sequence of Japanese quail (Coturnix coturnix japonica)JOURNAL OF HEREDITYIF2.52000-09-0129OAAI
Molecular dynamics of MHC genesis unraveled by sequence analysis of the 1,796,938-bp HLA class I regionPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAIF9.11999-11-09164OAAI
Nucleotide sequencing analysis of the 146-kilobase segment around the IkBL and MICA genes at the centromeric end of the HLA class I regionGENOMICSIF31998-02-0182PRE