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Kazuhiro R Nitta

5PUBLICATIONS

36CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)NeonatologyCell and nuclear divisionMedical infection agents (incl. prions)

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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

Frequent Collaborators

4 joint publications

Yasushi Okazaki

3 joint publications

Akira Ohtake

3 joint publications

Kei Murayama

3 joint publications

Masaru Shimura

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