Results
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491.
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ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19. [electronic resource] by
- Takahashi, Yuji
- Fukuda, Yoko
- Yoshimura, Jun
- Toyoda, Atsushi
- Kurppa, Kari
- Moritoyo, Hiroyoko
- Belzil, Veronique V
- Dion, Patrick A
- Higasa, Koichiro
- Doi, Koichiro
- Ishiura, Hiroyuki
- Mitsui, Jun
- Date, Hidetoshi
- Ahsan, Budrul
- Matsukawa, Takashi
- Ichikawa, Yaeko
- Moritoyo, Takashi
- Ikoma, Mayumi
- Hashimoto, Tsukasa
- Kimura, Fumiharu
- Murayama, Shigeo
- Onodera, Osamu
- Nishizawa, Masatoyo
- Yoshida, Mari
- Atsuta, Naoki
- Sobue, Gen
- Fifita, Jennifer A
- Williams, Kelly L
- Blair, Ian P
- Nicholson, Garth A
- Gonzalez-Perez, Paloma
- Brown, Robert H
- Nomoto, Masahiro
- Elenius, Klaus
- Rouleau, Guy A
- Fujiyama, Asao
- Morishita, Shinichi
- Goto, Jun
- Tsuji, Shoji
Producer: 20131230
In:
American journal of human genetics vol. 93
Availability: No items available.
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492.
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493.
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494.
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Expression and identification of a new splice variant of neuroglycan C, a transmembrane chondroitin sulfate proteoglycan, in the human brain. [electronic resource] by
- Aono, Sachiko
- Tokita, Yoshihito
- Yasuda, Yoko
- Hirano, Kanako
- Yamauchi, Shinobu
- Shuo, Takuya
- Matsui, Fumiko
- Keino, Hiroomi
- Kashiwai, Akiko
- Kawamura, Noriko
- Shimada, Atsuyoshi
- Kishikawa, Masao
- Asai, Mitsuoki
- Oohira, Atsuhiko
Producer: 20060329
In:
Journal of neuroscience research vol. 83
Availability: No items available.
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