Identification and characterization of a new member of the TNF family that induces apoptosis

Steven R. Wiley, Ken Schooley, Pamela J. Smolak, +8

Immunity

InflammationCytokineSignaling PathwayMedicineReceptor Tyrosine Kinase +10

DNAM-1, A Novel Adhesion Molecule Involved in the Cytolytic Function of T Lymphocytes

Akira Shibuya, David G. Campbell, Charles Hannum, +8

Immunity

Lymphocyte DevelopmentNatural SciencesCell AdhesionCytolytic FunctionImmunology +10

YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction

Michele Gabriele, Anneke T. Vulto‐van Silfhout, Pierre‐Luc Germain, +48

The American Journal of Human Genetics

Further Characterization of Proteins Associated with Elastic Fiber Microfibrils Including the Molecular Cloning of MAGP-2 (MP25)

Mark A. Gibson, George Hatzinikolas, Jaliya Kumaratilake, +4

Journal of Biological Chemistry

EngineeringHuman Mp25Cell AdhesionFiber SpinningCytoskeleton +19

AMP‐activated protein kinase isoenzyme family: subunit structure and chromosomal location

David Stapleton, Erica Woollatt, Ken I. Mitchelhill, +7

FEBS Letters

Rare copy number variation in cerebral palsy

G. McMichael, Santhosh Girirajan, Andrés Moreno-De-Luca, +9

European Journal of Human Genetics

Neurological DisorderProgressive Supranuclear PalsyBrain InjuryNeurologyCerebral Palsy +2

Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders

Ching Moey, Susan J. Hinze, Louise Brueton, +8

European Journal of Human Genetics

Neurodevelopmental DisordersKdm5c GenesBrain DevelopmentGenetic DisorderGenetics +10

Cloning of Human Lymphocyte-Specific Interferon Regulatory Factor (hLSIRF/hIRF4) and Mapping of the Gene to 6p23–p25

Alex Grossman, Hans-Willi Mittrücker, Jillian Nicholl, +7

Genomics

ImmunogeneticsTranscriptional RegulationLymphocyte DevelopmentImmune Cell DevelopmentGenetics +9

Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4

Leonie M. Quinn, Brett V. Johnson, Jillian Nicholl, +2

Gene

EmbryologyHuman PlacentaDevelopmental BiologyGenetic DisorderGenetics +7

Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma

Owen M. Siggs, Emmanuelle Souzeau, Deepa Taranath, +16

Ophthalmology