Publications



Microarray-related Project

1. Gene expression profile in rat renal isografts from brain death donors.
Kusaka M, Yamada K, Kuroyanagi A, Terauchi H, Kowa H, Kurahashi H. Hoshinaga K. Transplant Proc 37(1):364-366, 2005.

2. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-a2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T. Biochem Biophys Res Commun 342(2):489-502, 2006.

3. Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in a-dystroglycanopathies.
Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T. Hum Mol Genet 15(8):1279-89, 2006.

4. Analysis of gene expression profiles by oligonucleotide microarray in children with influenza.
Kawada J, Kimura H, Kamachi Y, Nishikawa K, Taniguchi M, Nagaoka K, Kurahashi H, Kojima S, Morishima T. J Gen Virol 87(6):1677-83, 2006.

5. Up-regulation of osteopontin, chemokines, adhesion molecule, and heat shock proteins in 1-hour biopsy from cardiac death donor kidneys.
Kusaka M, Kuroyanagi Y, Mori T, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K.
Transplant Proc 38(10):3347-3350, 2006.

6. Microarray analysis of differentially expressed fetal genes in placental tissue derived from early and late onset severe pre-eclampsia.
Nishizawa H, Pryor-Koishi K, Kato T, Kowa H, Kurahashi H, Udagawa Y. Placenta 28(5-6):487-97, 2007.

7. Genome-wide expression profile in rat model of renal isografts from brain dead donors.
Kusaka M, Kuroyanagi Y, Kowa H, Nagaoka K, Mori T, Yamada K, Taniguchi M, Shiroki R, Kurahashi H, Hoshinaga K. Transplantation 83(1):62-70, 2007.

8. Overexpression of FLRG in placenta and maternal serum in severe pre-eclampsia.
Pryor-Koishi K, Nishizawa H, Kato T, Kogo H, Murakami T, Tsuchida K, Kurahashi H, Udagawa Y. BJOG 114(9):1128-37, 2007.

9. Serum neutrophil gelatinase-associated lipocalin as a predictor of organ recovery from delayed graft function after kidney transplantation applying donation after cardiac death.
Kusaka M, Kuroyanagi Y, Mori T, Nagaoka K, Sasaki H, Maruyama T, Hayakawa K, Shiroki R, Kurahashi H, Hoshinaga K. Cell Transplant, in press.

10. Global gene expression profiling on renal scarring in rat model of pyelonephritis.
Ichino M, Mori T, Kusaka M, Kuroyanagi Y, Ishikawa K, Shiroki R, Kowa H, Kurahashi H, Hoshinaga K. Pediatr Nephrol, in press.



Others

1. Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.
Kurahashi H, Inagaki H, Yamada K, Ohye T, Taniguchi M, Emanuel BS, Toda T. J Biol Chem 279(34): 35377-35383, 2004.

2. Androgen Receptor Pathway in Rats with Autosomal Dominant Polycystic Kidney Disease.
Nagao S, Kusaka M, Nishii K, Marunouchi T, Kurahashi H, Takahashi H, Grantham J. J Am Soc Nephrol 16(7):2052-2062, 2005.

3. A palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved among primates.
Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H. Hum Mutat 26(4):332-42, 2005.

4. Genetic variation affects de novo translocation frequency.
Kato T, Inagaki H, Yamada K, Kogo H, Ohye T, Kowa H, Nagaoka K, Taniguchi M, Emanuel BS, Kurahashi H. Science 311(5763):971, 2006.

5. Molecular analysis of a mouse orthologue of HSFY, a candidate for the azoospermic factor on the human Y chromosome.
Kinoshita K, Shinka T, Sato Y, Kurahashi H, Kowa H, Chen G, Umeno M, Toida K, Kiyokage E, Nakano T, Ito S, Nakahori Y. J Med Invest 53(1-2):117-122, 2006.

6. Chromosomal translocations mediated by palindromic DNA.
Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS. Cell Cycle 5(12):1297-1303, 2006.

7. Increased water intake decreases progression of polycystic kidney disease in the PCK rat.
Nagao S, Nishii K, Katsuyama M, Kurahashi H, Marunouchi T, Takahashi H, Wallace DP. J Am Soc Nephrol 17(8):2220-2227, 2006.

8. Palindrome-mediated chromosomal translocations in humans.
Kurahashi H, Inagaki H, Kogo H, Ohye T, Kato T, Emanuel BS. DNA Repair 5(9-10):1136-1145, 2006.

9. Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22).
Ashley T, Gaeth AP, Inagaki H, Seftel A, Cohen MM, Anderson L, Kurahashi H, Emanuel BS. Am J Hum Genet 79(3):524-538, 2006.

10. Candidate genes for male factor infertility-validation.
Mori T, Kurahashi H, Shinka T, Nakahori Y, Taniguchi M, Toda T, Iwamoto T. Fertil Steril 86(5):1553-1554, 2006.

11. CDH1 is a specific marker for undifferentiated spermatogonia in mouse testes.
Tokuda M, Kadokawa Y, Kurahashi H, Marunouchi T. Biol Reprod 76(1):130-141, 2007.

12. Molecular clonong of a translocation hotspot in 22q11.
Kurahashi H, Inagaki H, Hosoba E, Kato T, Ohye T, Kogo H, Emanuel BS. Genome Res 17(4):461-9, 2007.

13. Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.
Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Emanuel BS, Kurahashi H. Fertil Steril 88(5):1446-8, 2007.

14. Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.
Kogo H, Inagaki H, Ohye T, Kato T, Emanuel BS, Kurahashi H. Nucleic Acids Res 35(4):1198-208, 2007.

15. The etiological role of allogeneic fetal rejection in pre-eclampsia.
Nishizawa H, Hasegawa K, Suzuki M, Achiwa Y, Kato T, Saito K, Kurahashi H, Udagawa Y. Am J Reprod Immunol 58(1):11-20, 2007.

16. Calcium channel inhibition with verapamil accelerates polycystic kidney disease progression in the Cy/+ rat.
Nagao S, Nishii K, Yoshihara D, Kurahashi H, Nagaoka K, Yamashita T, Takahashi H, Yamaguchi T, Calvet JP, Wallace DP. Kidney Int 73(3):269-77, 2008.

17. Mouse model for allogeneic fetal rejection recapitulates human pre-eclampsia.
Nishizawa H, Hasegawa K, Suzuki M, Achiwa Y, Kato T, Saito K, Kurahashi H, Udagawa Y. J Obstet Gynaecol Res, in press.

18. Two different forms of palindrome resolution in the human genome: deletion or translocation.
Kato T, Inagaki H, Kogo H, Ohye T, Yamada K, Emanuel BS, Kurahashi H. Hum Mol Genet, in press.