Cloning and Characterization of Three Novel Genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the Juvenile Amyotrophic Lateral Sclerosis (ALS2) Critical Region at Chromosome 2q33–q34: Candidate Genes for ALS2

This publication has 44 references indexed in Scilit:

• Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II
  Cell, 1999
• A Yeast Artificial Chromosome-Based Physical Map of the Juvenile Amyotrophic Lateral Sclerosis (ALS2) Critical Region on Human Chromosome 2q33–q34
  Genomics, 1999
• Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus ( ALS2 ) on chromosome 2q33
  neurogenetics, 1998
• Identification and Primary Structure of Five Human NADH-Ubiquinone Oxidoreductase Subunits
  Biochemical and Biophysical Research Communications, 1997
• Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
  Nucleic Acids Research, 1997
• Involvement of MACH, a Novel MORT1/FADD-Interacting Protease, in Fas/APO-1- and TNF Receptor–Induced Cell Death
  Cell, 1996
• Mouse and Human Homologues of the Yeast Origin of Replication Recognition Complex Subunit ORC2 and Chromosomal Localization of the Cognate Human Gene ORC2L
  Genomics, 1996
• A huntingtin-associated protein enriched in brain with implications for pathology
  Nature, 1995
• Prediction of the Coding Sequences of Unidentified Human Genes. I. The Coding Sequences of 40 New Genes (KIAA0001-KIAA0040) Deduced by Analysis of Randomly Sampled cDNA Clones from Human Immature Myeloid Cell Line KG-1 (Supplement)
  DNA Research, 1994
• Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
  Nature, 1993