E-LIB Suche - Ergebnisse für: Qin, Zailong

1

LncRNA sequencing reveals an essential role for the lncRNA-..:

Cao, Jian ; Du, Lin ; Zhao, Xueheng...
Genes & Immunity. , 2024

Link: https://doi.org/10.1038/..

2

Upregulation of CALD1 predicted a poor prognosis for platin..:

Li, Wei ; Huang, Limei ; Qi, Nana..
BMC Genomics. 25 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

3

Clinical and genetic analysis of trichohepatoneurodevelopme..:

Yang, Qi ; Zhou, Xunzhao ; Ling, Yeying...
Heliyon. 10 (2024) 6 - p. e27955 , 2024

Link: https://doi.org/10.1016/..

4

Malformations of cortical development: Fetal imaging and ge..:

Wang, Lin‐Lin ; Pan, Ping‐Shan ; Ma, Hui...
Molecular Genetics & Genomic Medicine. 12 (2024) 4 - p. , 2024

Link: https://doi.org/10.1002/..

5

Novel variants in TNRC6B cause global developmental delay w..:

Yang, Qi ; Ou, Shan ; Zhou, Xunzhao...
Molecular Genetics & Genomic Medicine. 12 (2024) 2 - p. , 2024

Link: https://doi.org/10.1002/..

6

A novel variant in NSUN2 causes intellectual disability in ..:

Yang, Qi ; Zhang, Qiang ; Qin, Zailong..
BMC Medical Genomics. 17 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

7

Novel germline variants in KMT2C in Chinese patients with K..:

Yang, Qi ; Zhang, Qiang ; Yi, Sheng...
Frontiers in Neurology. 15 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

8

Integration of single-cell and bulk RNA sequencing data rev..:

Zhang, Ming ; Ju, Yikun ; Xue, Lei...
Journal of Cancer. 15 (2024) 12 - p. 3890-3902 , 2024

Link: https://doi.org/10.7150/..

9

Clinical features and molecular genetic investigation of in..:

Zhang, Qiang ; Yang, Qi ; Luo, Jingsi...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

10

Single Cell Map of Human Azoospermia Testis Caused by Cyclo..:

Cao, Jian ; Zhao, Xueheng ; Qin, Zailong...
Scientific Data. 11 (2024) 1 - p. , 2024

Link: https://doi.org/10.1038/..

11

A genetic variant in the MAST1 gene is associated with mega..:

Yi, Sheng ; Tang, Xianglian ; Chen, Fei...
Molecular Genetics & Genomic Medicine. 12 (2024) 1 - p. , 2024

Link: https://doi.org/10.1002/..

12

Novel loss-of-function variants in WDR26 cause Skraban-Dear..:

Yang, Qi ; Zhou, Xunzhao ; Yi, Sheng...
Frontiers in Pediatrics. 12 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

13

A nonsense CC2D1A variant is associated with congenital ano..:

Yi, Sheng ; Tang, Xianglian ; Zhang, Qiang...
Heliyon. 10 (2024) 6 - p. e27946 , 2024

Link: https://doi.org/10.1016/..

14

Compound heterozygous WDR19 variants associated with nephro..:

Tang, Xianglian ; Yi, Sheng ; Qin, Zailong...
Heliyon. 10 (2024) 1 - p. e23257 , 2024

Link: https://doi.org/10.1016/..

15

Phenotypic and genotypic characterization of NPRL3‐related ..:

Yang, Dongling ; Wang, Jinqiu ; Qin, Zailong...
Epilepsia Open. 9 (2023) 1 - p. 33-40 , 2023

Link: https://doi.org/10.1002/..