Suchergebnisse - "Lou, Guiyu"

PubPharm (54)

1

Competing Endogenous RNAs Crosstalk in Hippocampus : A Potential Mechanism for Neuronal Developing Defects in Down Syndrome

enthalten in: Journal of molecular neuroscience : MN | 2024

von Zhao, H. | Lou, G. | Shao, Y. | +6

2

Competing Endogenous RNAs Crosstalk in Hippocampus: A Potential Mechanism for Neuronal Developing Defects in Down Syndrome

enthalten in: Journal of molecular neuroscience | 2024

von Zhao, H. | Lou, G. | Shao, Y. | +6

3

Application of whole exome sequencing for the inferential analysis of recessive genetic disease carrier status for couples with a child died of Primary immunodeficiency

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024

von Zhang, B. | Yang, K. | Zhang, Y. | +6

4

Construction method and application of EIF2S3 gene conditional systemic knockout mouse model

enthalten in: Europäisches Patentamt | 2023

von LOU GUIYU | ZHANG YUWEI | MA XINRUI | +2

5

Construction method and application of EIF2S3 gene conditional systemic knockout mouse model

enthalten in: Europäisches Patentamt | 2023

von LOU GUIYU | ZHANG YUWEI | MA XINRUI | +2

6

Expert consensus on the genetic diagnosis for Dystrophinopathies

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023

von Lou, G. | Hou, Q. | Qi, N. | +2

7

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023

von Zhang, W. | Qi, N. | Guo, L. | +4

8

Functional analysis of a novel nonsense variant c.91A>T of the TRAPPC2 gene in a Chinese family with X-linked recessive autosomal spondyloepiphyseal dysplasia tarda

enthalten in: Frontiers in genetics | 2023

von Lou, G. | Zhao, Y. | Zhao, H. | +5

9

Analysis of a child with mental retardation due to a de novo variant of the KAT6A gene

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2022

von Ren, Z. | Lei, X. | Zeng, M. | +6

10

Expert consensus on the application of prenatal exome sequencing for fetal structural anomalies

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2022

von Application Collaboration Group Of Whole Exome Sequencing In Prenatal Diagnosis | Lou, G. | Hou, Q. | +2

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