Suchergebnisse - "He, Jie"

PubPharm (69)

1

A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma

enthalten in: Cell | 2024

von Verma, S. | Gudiseva, H. | Chavali, V. | +57

CommentIn: Cell. 2024 Jan 18;187(2):273-275. - PMID 38242084

2

A Novel HRD Signature Is Predictive of FOLFIRINOX Benefit in Metastatic Pancreatic Cancer

enthalten in: The oncologist | 2023

von Chen, K. | Madison, R. | Moore, J. | +14

3

N-acetylcysteine and cysteamine bitartrate prevent azide-induced neuromuscular decompensation by restoring glutathione balance in two novel surf1-/- zebrafish deletion models of Leigh syndrome

enthalten in: Human molecular genetics | 2023

von Haroon, S. | Yoon, H. | Seiler, C. | +10

4

Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix

enthalten in: Cell reports | 2023

von Nigro, P. | Vamvini, M. | Yang, J. | +15

5

Health Impairments in Children and Adolescents After Hospitalization for Acute COVID-19 or MIS-C

enthalten in: Pediatrics | 2022

von Maddux, A. | Berbert, L. | Young, C. | +38

6

Modeling and Designing Particle-Regulated Amyloid-like Assembly of Synthetic Polypeptides in Aqueous Solution

enthalten in: Biomacromolecules | 2022

von Yang, T. | Benson, K. | Fu, H. | +9

7

Single Cell Sequencing of Induced Pluripotent Stem Cell Derived Retinal Ganglion Cells (iPSC-RGC) Reveals Distinct Molecular Signatures and RGC Subtypes

enthalten in: Genes | 2021

von Gudiseva, H. | Vrathasha, V. | He, J. | +3

8

LMX1B Locus Associated with Low-Risk Baseline Glaucomatous Features in the POAAGG Study

enthalten in: Genes | 2021

von Meer, E. | Qin, V. | Gudiseva, H. | +8

9

Co-occurring gain-of-function mutations in HER2 and HER3 modulate HER2/HER3 activation, oncogenesis, and HER2 inhibitor sensitivity

enthalten in: Cancer cell | 2021

von Hanker, A. | Brown, B. | Meiler, J. | +15

CommentIn: Cell Rep Med. 2021 Aug 06;2(8):100361. - PMID 34467245

10

RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)

enthalten in: Human molecular genetics | 2021

von Moreno-Leon, L. | West, E. | O'Hara-Wright, M. | +11

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