●柳沢比呂子　（やなぎさわひろこ）
1	Sango, K., Yanagisawa, H. and Takaku, S. Expression and histochemical localization of ciliary neurotrophic factor in cultured adult rat dorsal root ganglion neurons. Histochem. Cell Biol., 128:35-43 (2007).
2	Sango K, Suzuki T, Yanagisawa H, Takaku S, Hirooka M, Tamura M, Watabe K. High glucose-induced activation of the polyol pathway and changes of gene expression profiles in immortalized adult mouse Schwann cells IMS32.  J. Neurochem. 98, 446-458. (2006).
3	HSpin1, a transmembrane protein interacting with Bcl-2/Bcl-xL, induces a caspase- independent autophagic cell death. Cell Death Differ. 10, 798-807, 2003. Yanagisawa H, Miyashita T, Nakano Y and Yamamoto D.
4	HSpin1 interacts with Bcl-2 and BclxL, and induces autophagic cell death. " Programmed cell death": Cold Spring Harbor Laboratory meeting, Hiroko Yanagisawa, Toshiyuki Miyashita and Daisuke Yamamoto. September 17-21, 2003
5	Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine. Yanagisawa H, Bundo M, Miyashita T, Okamura-Oho Y, Tadokoro K, Tokunaga K,Yamada M. Hum Mol Genet. 2000 May 22;9(9):1433-42.
6	Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms,are also responsible for Frasier syndrome. Kohsaka T, Tagawa M, Takekoshi Y, Yanagisawa H, Tadokoro K, Yamada M. 1999;14(6):466-70.
7	Intracellular aggregate formation of dentatorubral-pallidoluysian atrophy (DRPLA) protein with the extended polyglutamine. Miyashita T, Nagao K, Ohmi K, Yanagisawa H, Okamura-Oho Y,Yamada M. Biochem Biophys Res Commun. 1998 Aug 10;249(1):96-102.
8	PAX6 missense mutation in isolated foveal hypoplasia.Azuma N, Nishina S, Yanagisawa H, Okuyama T, Yamada M. Nat Genet. 1996 Jun;13(2):141-2.
9	Different origins of expanded repeats for Haw River syndrome and dentatorubral-pallidoluysian atrophy. Potter NT, Yanagisawa H, Yamada M. Lancet. 1996 May 4;347(9010):1271.
10	Unique origin and multistep process for the generation of expanded DRPLA triplet repeats. Yanagisawa H, Fujii K, Nagafuchi S, Nakahori Y, Nakagome Y, Akane A,Nakamura M, Sano A,Komure O, Kondo I, Jin DK, Sorensen SA, Potter NT, Young SR, Nakamura K,Nukina N, Nagao Y,Tadokoro K, Okuyama T, Miyashita T, Inoue T, Kanazawa I, Yamada M. Hum Mol Genet. 1996 Mar;5(3):373-9.
11	Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA). Nagafuchi S, Yanagisawa H, Ohsaki E, Shirayama T, Tadokoro K, Inoue T,Yamada M. Nat Genet. 1994 Oct;8(2):177-82.
12	Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nagafuchi S, Yanagisawa H, Sato K, Shirayama T, Ohsaki E, Bundo M, Takeda T,Tadokoro K, Kondo I, Murayama N, et al. Nat Genet. 1994 Jan;6(1):14-8.
13	A novel mutation of the WT1 gene (a tumor suppressor gene for Wilms' tumor) in a patient with Denys-Drash syndrome. Sakai A, Tadokoro K, Yanagisawa H, Nagafuchi S, Hoshikawa N, Suzuki T, Kohsaka T, Hasegawa T, Nakahori Y, Yamada M. Hum Mol Genet. 1993 Nov;2(11):1969-70.