Suchergebnisse - "Zaib, Tahir"

PubPharm (15)

1

CD22 is a potential target of CAR-NK cell therapy for esophageal squamous cell carcinoma

enthalten in: Journal of translational medicine | 2023

von Liu, T. | Dai, X. | Xu, Y. | +8

2

CD22 is a potential target of CAR-NK cell therapy for esophageal squamous cell carcinoma

enthalten in: Journal of translational medicine | 2023

von Liu, T. | Dai, X. | Xu, Y. | +8

3

Expression of CD22 in Triple-Negative Breast Cancer : A Novel Prognostic Biomarker and Potential Target for CAR Therapy

enthalten in: International journal of molecular sciences | 2023

von Zaib, T. | Cheng, K. | Liu, T. | +10

4

Recent Advances in Syndactyly : Basis, Current Status and Future Perspectives

enthalten in: Genes | 2022

von Zaib, T. | Rashid, H. | Khan, H. | +2

5

Two SNPs rs1801133 and rs1801394 in folate pathway are associated with the risk of nonsyndromic cleft lip with or without cleft palate

enthalten in: ResearchSquare.com | 2021

von Author), Q. | Xu, L. | Jia, X. | +4

6

Two SNPs rs1801133 and rs1801394 in folate pathway are associated with the risk of nonsyndromic cleft lip with or without cleft palate

enthalten in: ResearchSquare.com | 2021

von Li, Q. | Xu, L. | Jia, X. | +3

7

Emodin succinyl ester inhibits malignant proliferation and migration of hepatocellular carcinoma by suppressing the interaction of AR and EZH2

enthalten in: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie | 2020

von Khan, H. | Jia, W. | Yu, Z. | +7

8

Combinatorial approach of in silico and in vitro evaluation of MLH1 variant associated with Lynch syndrome like metastatic colorectal cancer

enthalten in: Bioscience reports | 2020

von Saleem, K. | Zaib, T. | Ji, W. | +12

ExpressionOfConcernIn: Biosci Rep. 2020 Jun 26;40(6):. - PMID 32579207

9

SNPs in folate pathway are associated with the risk of nonsyndromic cleft lip with or without cleft palate, a meta-analysis

enthalten in: Bioscience reports | 2020

von Li, Q. | Xu, L. | Jia, X. | +4

10

Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree

enthalten in: Disease markers | 2020

von Zaib, T. | Zhang, C. | Saleem, K. | +15

RetractionIn: Dis Markers. 2023 Jul 12;2023:9784325. - PMID 37476627