Kazuhiro R Nitta
5PUBLICATIONS
36CO-AUTHORS
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Publications (5)
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|Sep 02, 2022
Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single-cell level in individuals with mitochondrial disease.Atsuko Imai-Okazaki, Kazuhiro R Nitta, Yukiko Yatsuka
|Oct 09, 2021
Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis.Tomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama
|Aug 18, 2021
Genome sequencing and RNA-seq analyses of mitochondrial complex I deficiency revealed Alu insertion-mediated deletion in NDUFV2.Yoshihito Kishita, Masaru Shimura, Masakazu Kohda
|May 10, 2020
A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency.Yukiko Yatsuka, Yoshihito Kishita, Luke E Formosa
|May 06, 2017
Impact of cytosine methylation on DNA binding specificities of human transcription factors.Yimeng Yin, Ekaterina Morgunova, Arttu Jolma
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Frequent Collaborators
4 joint publications
Yasushi Okazaki
3 joint publications
Akira Ohtake
3 joint publications
Kei Murayama
3 joint publications
Masaru Shimura
3 joint publications
Yoshihito Kishita
3 joint publications
Yukiko Yatsuka
2 joint publications
Takuya Fushimi
2 joint publications
Atsuko Imai-Okazaki
1 joint publications
Ekaterina Morgunova
1 joint publications
Pratyush K Das
