Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

Zemin Deng, Jane H. Morse, Susan L. Slager, +9

The American Journal of Human Genetics

HypertensionGene Pph1Developmental BiologyPulmonary Arterial HypertensionGenetic Disorder +9

TRANCE Is a Novel Ligand of the Tumor Necrosis Factor Receptor Family That Activates c-Jun N-terminal Kinase in T Cells

Brian Wong, Jaerang Rho, Joseph R. Arron, +9

Journal of Biological Chemistry

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

Sergey Kalachikov, Oleg V. Evgrafov, Barbara Ross, +15

Nature Genetics

Auditory ProcessingMendelian DisorderNeurophysiologyGenetic DisorderGenetics +7

Transcriptional Repressor Blimp-1 Promotes CD8+ T Cell Terminal Differentiation and Represses the Acquisition of Central Memory T Cell Properties

Rachel L. Rutishauser, Gislâine A. Martins, Sergey Kalachikov, +6

Immunity

Signal TransductionT-regulatory CellImmunologyGene ExpressionMedicine +2

The Genomic Sequence of the Accidental Pathogen <i>Legionella pneumophila</i>

Minchen Chien, Irina Morozova, Shundi Shi, +34

Science

Pathogenic MicrobiologyMicrobial PathogensMedicineGeneticsPathogenesis +13

Neuronal Transcriptome of Aplysia: Neuronal Compartments and Circuitry

Leonid L. Moroz, John R. Edwards, Sathyanarayanan V. Puthanveettil, +20

Cell

Neuronal TranscriptomeMolecular NeuroscienceNeuroanatomyNeuroscienceNeurotransmission +5

Evidence for Acquisition of <i>Legionella</i> Type IV Secretion Substrates via Interdomain Horizontal Gene Transfer

Karim Suwwan de Felipe, Sergey Pampou, Oliver S. Jovanovic, +4

Journal of Bacteriology

Quantitative evaluation of all hexamers as exonic splicing elements

Shengdong Ke, Shulian Shang, Sergey Kalachikov, +5

Genome Research

<i>LGI1</i> mutations in autosomal dominant partial epilepsy with auditory features

Ruth Ottman, Melodie R. Winawer, Sergey Kalachikov, +4

Neurology

Nucleotide sequence, transcription map, and mutation analysis of the 13q14 chromosomal region deleted in B-cell chronic lymphocytic leukemia

Anna Migliazza, Francesc Bosch, Hirokazu Komatsu, +16

Blood