|1.||Hasegawa, Hiroshi: 1 article (12/2015)|
|2.||Omoteyama, Kazuki: 1 article (12/2015)|
|3.||Okamoto, Kazuki: 1 article (12/2015)|
|4.||Suzuki, Itsuku: 1 article (12/2015)|
|5.||Arito, Mitsumi: 1 article (12/2015)|
|6.||Kato, Tomohiro: 1 article (12/2015)|
|7.||Sato, Toshiyuki: 1 article (12/2015)|
|8.||Suematsu, Naoya: 1 article (12/2015)|
|9.||Yamaguchi, Noboru: 1 article (12/2015)|
|10.||Maedomari, Mioto: 1 article (12/2015)|
|1.||Autistic Disorder (Autism)
01/01/1995 - "DR-positive T cells in autism: association with decreased plasma levels of the complement C4B protein."
02/01/1994 - "Decreased plasma concentrations of the C4B complement protein in autism."
01/01/1992 - "We previously reported that the complement C4B null allele appears to be associated with infantile autism. "
03/01/1991 - "Increased frequency of the null allele at the complement C4b locus in autism."
|2.||Schizophrenia (Dementia Praecox)
|3.||Attention Deficit Disorder with Hyperactivity (Attention Deficit Hyperactivity Disorder)
01/01/1997 - "The objective was to determine whether a relationship exists among the complement C4B gene, a DR region gene and attention deficit hyperactivity disorder (ADHD). "
08/01/1995 - "Is decreased blood plasma concentration of the complement C4B protein associated with attention-deficit hyperactivity disorder?"
|4.||Congenital Adrenal Hyperplasia (Hyperplasia, Congenital Adrenal)
05/01/1986 - "Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein."
11/01/1987 - "HLA-Bw47, a rare human histocompatibility antigen, occurs in strong linkage disequilibrium with HLA-A3,Cw6,DR7 and salt-losing congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and is associated with a contiguous deletion of the active CA21HB gene and the C4B complement gene. "
|3.||Adenosine A1 Receptor
|4.||Vitamin D-Binding Protein
|5.||Steroid 21-Hydroxylase (21 Hydroxylase)
|6.||Proteins (Proteins, Gene)