Rare earth elements in paddy fields from eroded granite hilly land in a southern China watershed

por Chen, Haibin, Chen, Zhibiao, Chen, Zhiqiang, Ma, Qianyi, Zhang, Qingqing
Publicado 2019

Histamine H(2) receptor negatively regulates oligodendrocyte differentiation in neonatal hypoxic-ischemic white matter injury

por Jiang, Lei, Cheng, Li, Chen, Han, Dai, Haibin, An, Dadao, Ma, Qianyi, Zheng, Yanrong, Zhang, Xiangnan, Hu, Weiwei, Chen, Zhong
Publicado 2020

Regulation of meiotic progression by Sertoli-cell androgen signaling

por Larose, Hailey, Kent, Travis, Ma, Qianyi, Shami, Adrienne Niederriter, Harerimana, Nadia, Li, Jun Z., Hammoud, Saher Sue, Handel, Mary Ann
Publicado 2020

Good's buffers have various affinities to gold nanoparticles regulating fluorescent and colorimetric DNA sensing

por Jimmy Huang, Po-Jung, Yang, Jeffy, Chong, Kellie, Ma, Qianyi, Li, Miao, Zhang, Fang, Moon, Woohyun J., Zhang, Guomei, Liu, Juewen
Publicado 2020

Histamine H(2) receptor deficit in glutamatergic neurons contributes to the pathogenesis of schizophrenia

por Ma, Qianyi, Jiang, Lei, Chen, Han, An, Dadao, Ping, Yiting, Wang, Yujia, Dai, Haibin, Zhang, Xiangnan, Wang, Yi, Chen, Zhong, Hu, Weiwei
Publicado 2023

Electrolyte Design for Lithium Metal Anode‐Based Batteries Toward Extreme Temperature Application

por Luo, Dan, Li, Matthew, Zheng, Yun, Ma, Qianyi, Gao, Rui, Zhang, Zhen, Dou, Haozhen, Wen, Guobin, Shui, Lingling, Yu, Aiping, Wang, Xin, Chen, Zhongwei
Publicado 2021

SAT-291 SIX3 Is Essential for Hypothalamic and Pituitary Development

por Bando, Hironori, Brinkmeier, Michelle L, Castinetti, Frederic, Gergics, Peter, Mortensen, Amanda H, Ozel, Ayse Bilge, Ma, Qianyi, Li, Jun Z, Brue, Thierry, Camper, Sally A
Publicado 2020

Nano-crumples induced Sn-Bi bimetallic interface pattern with moderate electron bank for highly efficient CO(2) electroreduction

por Ren, Bohua, Wen, Guobin, Gao, Rui, Luo, Dan, Zhang, Zhen, Qiu, Weibin, Ma, Qianyi, Wang, Xin, Cui, Yi, Ricardez–Sandoval, Luis, Yu, Aiping, Chen, Zhongwei
Publicado 2022

SIX3 Variant Causes Pituitary Stalk Interruption Syndrome and Combined Pituitary Hormone Deficiency

por Bando, Hironori, Brinkmeier, Michelle, Gergics, Peter, Fang, Qing, Mortensen, Amanda Helen, Ozel, Ayse Bilge, Ma, Qianyi, Li, Jun, Reynaud, Rachel, Castinetti, Frederic, Brue, Thierry Christian, Camper, Sally Ann
Publicado 2021

Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing

por Correa, Fernanda A., França, Marcela M., Fang, Qing, Ma, Qianyi, Bachega, Tania A., Rodrigues, Andresa, Ozel, Bilge A., Li, Jun Z., Mendonca, Berenice B., Jorge, Alexander A. L., Carvalho, Luciani R., Camper, Sally A., Arnhold, Ivo J. P
Publicado 2017

TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice

por Shen, Yu-chi, Shami, Adrienne Niederriter, Moritz, Lindsay, Larose, Hailey, Manske, Gabriel L., Ma, Qianyi, Zheng, Xianing, Sukhwani, Meena, Czerwinski, Michael, Sultan, Caleb, Chen, Haolin, Gurczynski, Stephen J., Spence, Jason R., Orwig, Kyle E., Tallquist, Michelle, Li, Jun Z., Hammoud, Saher Sue
Publicado 2021

SAT-LB58 Molecular Investigation of Recessive Inheritance by Exome Sequencing of Patients With Congenital Hypopituitarism

por Pereira Ferreira, Nathalia Garcia Bianchi, Madeira, Joao Luiz do Oliveira, Kertsz, Renata, Gergics, Peter, Benedetti, Anna Flavia Figueredo, Biscotto, Isabela Peixoto, Fang, Qing, Ma, Qianyi, Ozel, Bilge Ayse, Li, Jun, Camper, Sally Ann, Jorge, Alexander Augusto Lima, Mendonca, Berenice Bilharinho, Arnhold, Ivo J, Carvalho, Luciani Renata Silveira
Publicado 2020

The phenotypic spectrum associated with OTX2 mutations in humans

por Gregory, Louise C, Gergics, Peter, Nakaguma, Marilena, Bando, Hironori, Patti, Giuseppa, McCabe, Mark J, Fang, Qing, Ma, Qianyi, Ozel, Ayse Bilge, Li, Jun Z, Poina, Michele Moreira, Jorge, Alexander A L, Benedetti, Anna F Figueredo, Lerario, Antonio M, Arnhold, Ivo J P, Mendonca, Berenice B, Maghnie, Mohamad, Camper, Sally A, Carvalho, Luciani R S, Dattani, Mehul T
Publicado 2021

Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders

por Ferreira, Nathalia G B P, Madeira, Joao L O, Gergics, Peter, Kertsz, Renata, Marques, Juliana M, Trigueiro, Nicholas S S, Benedetti, Anna Flavia Figueredo, Azevedo, Bruna V, Fernandes, Bianca H V, Bissegatto, Debora D, Biscotto, Isabela P, Fang, Qing, Ma, Qianyi, Ozel, Asye B, Li, Jun, Camper, Sally A, Jorge, Alexander A L, Mendonça, Berenice B, Arnhold, Ivo J P, Carvalho, Luciani R
Publicado 2023

Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum

por Nakaguma, Marilena, Ferreira, Nathalia Garcia Bianchi Pereira, Benedetti, Anna Flavia Figueredo, Madi, Mariana Cotarelli, Silva, Juliana Moreira, Li, Jun Z., Ma, Qianyi, Bilge Ozel, Ayse, Fang, Qing, Narcizo, Amanda de Moraes, Cardoso, Laís Cavalca, Montenegro, Luciana Ribeiro, Funari, Mariana Ferreira de Assis, Nishi, Mirian Yumie, Arnhold, Ivo Jorge Prado, Jorge, Alexander Augusto de Lima, de Mendonca, Berenice Bilharinho, Camper, Sally Ann, Carvalho, Luciani R.
Publicado 2021