A citation-based method for searching scientific literature

H Chusho, N Tamura, Y Ogawa, A Yasoda, M Suda, T Miyazawa, K Nakamura, K Nakao, T Kurihara, Y Komatsu, H Itoh, K Tanaka, Y Saito, M Katsuki, K Nakao. Proc Natl Acad Sci U S A 2001
Times Cited: 327



Rumi Hachiya, Yuko Ohashi, Yasutomi Kamei, Takayoshi Suganami, Hiroshi Mochizuki, Norimasa Mitsui, Masaaki Saitoh, Masako Sakuragi, Gen Nishimura, Hirofumi Ohashi, Tomonobu Hasegawa, Yoshihiro Ogawa. J Clin Endocrinol Metab 2007
Times Cited: 48




List of shared articles



Times cited

Prevention of guanylyl cyclase-B dephosphorylation rescues achondroplastic dwarfism.
Brandon M Wagner, Jerid W Robinson, Yun-Wen Lin, Yi-Ching Lee, Nabil Kaci, Laurence Legeai-Mallet, Lincoln R Potter. JCI Insight 2021
1

Hormone resistance and short stature: A journey through the pathways of hormone signaling.
Renata C Scalco, Fernanda A Correa, Naiara C B Dantas, Gabriela A Vasques, Alexander A L Jorge. Mol Cell Endocrinol 2021
0

Role of NPR2 mutation in idiopathic short stature: Identification of two novel mutations.
Il Tae Hwang, Yusuke Mizuno, Naoko Amano, Hye Jin Lee, Young Suk Shim, Hyo-Kyoung Nam, Young-Jun Rhie, Seung Yang, Kee-Hyoung Lee, Tomonobu Hasegawa,[...]. Mol Genet Genomic Med 2020
8

Male mice with elevated C-type natriuretic peptide-dependent guanylyl cyclase-B activity have increased osteoblasts, bone mass and bone strength.
Jerid W Robinson, Nicholas C Blixt, Andrew Norton, Kim C Mansky, Zhou Ye, Conrado Aparicio, Brandon M Wagner, Andrew M Benton, Gordon L Warren, Sundeep Khosla,[...]. Bone 2020
5

A novel nonsense mutation in NPR2 gene causing Acromesomelic dysplasia, type Maroteaux in a consanguineous family in Southern Punjab (Pakistan).
Saima Mustafa, Zafrin Akhtar, Muhammad Latif, Mubashir Hassan, Muhammad Faisal, Furhan Iqbal. Genes Genomics 2020
2

Short Stature is Progressive in Patients with Heterozygous NPR2 Mutations.
Patrick C Hanley, Harsh S Kanwar, Corine Martineau, Michael A Levine. J Clin Endocrinol Metab 2020
4

Is C-type natriuretic peptide regulated by a feedback loop? A study on systemic and local autoregulatory effect.
Yohei Ueda, Keisho Hirota, Ichiro Yamauchi, Takuro Hakata, Takafumi Yamashita, Toshihito Fujii, Akihiro Yasoda, Nobuya Inagaki. PLoS One 2020
1

Exogenous C-type natriuretic peptide therapy for impaired skeletal growth in a murine model of glucocorticoid treatment.
Yohei Ueda, Akihiro Yasoda, Keisho Hirota, Ichiro Yamauchi, Takafumi Yamashita, Yugo Kanai, Yoriko Sakane, Toshihito Fujii, Nobuya Inagaki. Sci Rep 2019
4

Rats deficient C-type natriuretic peptide suffer from impaired skeletal growth without early death.
Toshihito Fujii, Keisho Hirota, Akihiro Yasoda, Akiko Takizawa, Naomi Morozumi, Ryuichi Nakamura, Takafumi Yotsumoto, Eri Kondo, Yui Yamashita, Yoriko Sakane,[...]. PLoS One 2018
8


The regulatory role of the kinase-homology domain in receptor guanylyl cyclases: nothing 'pseudo' about it!
Vishwas Mishra, Ridhima Goel, Sandhya S Visweswariah. Biochem Soc Trans 2018
6

Circulating osteocrin stimulates bone growth by limiting C-type natriuretic peptide clearance.
Yugo Kanai, Akihiro Yasoda, Keita P Mori, Haruko Watanabe-Takano, Chiaki Nagai-Okatani, Yui Yamashita, Keisho Hirota, Yohei Ueda, Ichiro Yamauchi, Eri Kondo,[...]. J Clin Invest 2017
18

Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia.
Jia Chen, Jiaqi Liu, Yangzhong Zhou, Sen Liu, Gang Liu, Yuzhi Zuo, Zhihong Wu, Nan Wu, Guixing Qiu. J Mol Med (Berl) 2017
2

Therapeutic effect of CNP on renal osteodystrophy by antagonizing the FGF-23/MAPK pathway.
Peng Hu, Bao Yu Huang, Xun Xia, Qiang Xuan, Bo Hu, Yuan Han Qin. J Recept Signal Transduct Res 2016
8

Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reports.
Wei Wang, Mi Hyun Song, Kohji Miura, Makoto Fujiwara, Nobutoshi Nawa, Yasuhisa Ohata, Taichi Kitaoka, Takuo Kubota, Noriyuki Namba, Dong Kyu Jin,[...]. Am J Med Genet A 2016
17

Genetics of human isolated acromesomelic dysplasia.
Saadullah Khan, Sulman Basit, Muzammil Ahmad Khan, Noor Muhammad, Wasim Ahmad. Eur J Med Genet 2016
9