Publications by authors named "Longlong Lin"

Claim this Profile
D
Demand Response Strategy Considering Industrial Loads and Energy Storage with High Proportion of Wind-Power Integration.
Chongyi Tian, Julin Li, Chunyu Wang, Longlong Lin, Yi Yan

Sensors (Basel)· November 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Effective Temporal Graph Learning via Personalized PageRank.
Ziyu Liao, Tao Liu, Yue He, Longlong Lin

Entropy (Basel)· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Preliminary Study on Clinical Characteristics and Pathogenesis of Mutations Patients.
Yun Ren, Xiaona Luo, Haiyan Tong, Simei Wang, Jinbin Yan, Longlong Lin

Pharmgenomics Pers Med· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Photovoltaic power prediction based on dilated causal convolutional network and stacked LSTM.
Chongyi Tian, Longlong Lin, Yi Yan, Ruiqi Wang, Fan Wang

Math Biosci Eng· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy.
Xiaoang Sun, Xiaona Luo, Longlong Lin, Simei Wang, Chunmei Wang

Mol Genet Genomic Med· September 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Design of a Switchable Filter for Reflectionless-Bandpass-to-Reflectionless-Bandstop Responses.
Gangxiong Wu, Hao Wu, Wei Qin, Jin Shi, Wei Zhang, Longlong Lin

Micromachines (Basel)· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Balanced Substrate Integrated Waveguide Phase Shifter with Wideband Common-Mode Suppression.
Wei Zhang, Jin Shi, Gangxiong Wu, Longlong Lin, Kai Xu

Micromachines (Basel)· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Segawa syndrome caused by gene mutation and its mechanism.
Yilin Wang, Chunmei Wang, Meiyan Liu, Wuhen Xu, Simei Wang, Longlong Lin

Front Genet· December 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Two heterozygous mutations in the calcium/calmodulin-dependent serine protein kinase gene (CASK) in cases with developmental disorders.
Kunfang Yang, Longlong Lin, Fang Yuan, Xiaoguang Li, Zhiping Liu, Yilin Wang

Mol Genet Genomic Med· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases.
Meiyan Liu, Xiaoang Sun, Longlong Lin, Xiaona Luo, Simei Wang

Front Pediatr· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Dual-Band, Dual-Polarized Filtering Antenna Based on Cross-Shaped Dielectric Strip Resonator.
Lixin Jin, Hui Tang, Jin Shi, Longlong Lin, Kai Xu

Micromachines (Basel)· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene.
Xiaona Luo, Yilin Wang, Fang Yuan, Longlong Lin, Anqi Wang

Stem Cell Res· July 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Study on the Clinical Phenotype and Function of HPRT1 Gene.
Miao Guo, Yucai Chen, Longlong Lin, Yilin Wang, Anqi Wang

Child Neurol Open· July 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs*28 (c.1507_1508del) in the ARX gene.
Chunmei Wang, Yilin Wang, Wuhen Xu, Xuefeng Lin, Jiaming Xi, Longlong Lin

Stem Cell Res· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Study of 8 Cases of Gene Mutation-Related Neurological Diseases and Their Mechanisms.
Xiaona Luo, Xiaoang Sun, Yilin Wang, Longlong Lin, Fang Yuan

Front Cell Dev Biol· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mechanisms of Congenital Myasthenia Caused by Three Mutations in the Gene.
Xiaona Luo, Chunmei Wang, Longlong Lin, Fang Yuan, Simei Wang, Yilin Wang

Front Pediatr· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13.
Simei Wang, Longlong Lin, Yilin Wang, Anqi Wang, Zhao Liu

J Neurol Sci· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome.
Yilin Wang, Fang Yuan, Anqi Wang, Chao Wang, Longlong Lin

Stem Cell Res· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome.
Anqi Wang, Jiaming Xi, Fang Yuan, Yilin Wang, Simei Wang, Longlong Lin

Stem Cell Res· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13.
Fang Yuan, Chunmei Wang, Jiaming Xi, Simei Wang, Longlong Lin, Yilin Wang

Stem Cell Res· May 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spectrum of Germline Mutations and Clinical Features in Unrelated Chinese Patients With Retinoblastoma.
Xiaoping Lan, Wuhen Xu, Xiaojun Tang, Haiyun Ye, Xiaozhen Song, Longlong Lin

Front Genet· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
-
-Related Disease in a Chinese Girl: Clinical Characteristics and Underlying Mechanism.
Chao Wang, Longlong Lin, Yan Xue, Yilin Wang, Zhao Liu

Front Genet· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
MicroRNA-588 suppresses tumor cell migration and invasion by targeting GRN in lung squamous cell carcinoma.
Li Qian, Longlong Lin, Yufeng Du, Xiaoyan Hao, Yuze Zhao

Mol Med Rep· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis