Søgeresultater - Ming Juan Ye
- Showing 1 - 6 results of 6
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1
Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome af Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, Yoshimi Nozu, Ming Juan Ye, Akemi Shono, Satoko Yamanouchi, Shogo Minamikawa, Naoya Morisada, Koichi Nakanishi, Yuko Shima, Norishige Yoshikawa, Takeshi Ninchoji, Ichiro Morioka, Hiroshi Kaito, Kazumoto Iijima
Udgivet 2017Artigo -
2
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome af Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, Naoya Morisada, Yoshimi Nozu, Ming Juan Ye, Aya Imafuku, Kenichiro Miura, Tomohiko Yamamura, Shogo Minamikawa, Akemi Shono, Takeshi Ninchoji, Ichiro Morioka, Koichi Nakanishi, Norishige Yoshikawa, Hiroshi Kaito, Kazumoto Iijima
Udgivet 2016Artigo -
3
Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome af Tomohiko Yamamura, Tomoko Horinouchi, China Nagano, Takashi Omori, Nana Sakakibara, Yuya Aoto, Shinya Ishiko, Koichi Nakanishi, Yuko Shima, Hiroaki Nagase, Hiroki Takeda, Rini Rossanti, Ming Juan Ye, Yoshimi Nozu, Shingo Ishimori, Takeshi Ninchoji, Hiroshi Kaito, Naoya Morisada, Kazumoto Iijima, Kandai Nozu
Udgivet 2020Artigo -
4
Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome af Ai Unzaki, Naoya Morisada, Kandai Nozu, Ming Juan Ye, Shuichi Ito, Tatsuo Matsunaga, Kenji Ishikura, Shihomi Ina, Koji Nagatani, Takayuki Okamoto, Yuji Inaba, Naoko Ito, Toru Igarashi, Shoichiro Kanda, Ken Ito, Kohei Omune, Takuma Iwaki, Kazuyuki Ueno, Mayumi Yahata, Yasufumi Ohtsuka, Eriko Nishi, Nobuya Takahashi, Tomoaki Ishikawa, Shunsuke Goto, Nobuhiko Okamoto, Kazumoto Iijima
Udgivet 2018Artigo -
5
Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome af Tomoko Horinouchi, Kandai Nozu, Tomohiko Yamamura, Shogo Minamikawa, Takashi Omori, Keita Nakanishi, Junya Fujimura, Akira Ashida, Mineaki Kitamura, Mitsuhiro Kawano, Wataru Shimabukuro, Chizuko Kitabayashi, Aya Imafuku, Keiichi Tamagaki, Koichi Kamei, Kenjirou Okamoto, Shuichiro Fujinaga, Masafumi Oka, Toru Igarashi, Akinori Miyazono, Emi Sawanobori, Rika Fujimaru, Koichi Nakanishi, Yuko Shima, Masafumi Matsuo, Ming Juan Ye, Yoshimi Nozu, Naoya Morisada, Hiroshi Kaito, Kazumoto Iijima
Udgivet 2018Artigo -
6
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 af Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, Maki Terakawa, Yutaka Takaoka, Kohei Omachi, Minoru Takasato, Kiyosumi Takaishi, Takao Shoji, Yoshiyuki Onishi, Yoshito Kanazawa, Makoto Koizumi, Yasuko Tomono, Aki Sugano, Akemi Shono, Shogo Minamikawa, China Nagano, Nana Sakakibara, Shinya Ishiko, Yuya Aoto, Misato Kamura, Yutaka Harita, Kenichiro Miura, Shoichiro Kanda, Naoya Morisada, Rini Rossanti, Ming Juan Ye, Yoshimi Nozu, Masafumi Matsuo, Hirofumi Kai, Kazumoto Iijima, Kandai Nozu
Udgivet 2020Artigo
Søgeredskaber:
Relaterede emner
Biology
Gene
Genetics
Kidney
Medicine
Alport syndrome
Glomerulonephritis
Internal medicine
Phenotype
Exon
Genotype
Alternative splicing
Bioinformatics
Dermatology
Genotype-phenotype distinction
Angiotensin II
Audiology
Biopsy
Cancer research
Comparative genomic hybridization
Copy-number variation
Correlation
Endocrinology
Exon skipping
Extracellular matrix
Genetic heterogeneity
Genome
Geometry
Glomerular basement membrane
Hearing loss