K. Sia

发表

An Efficient and Safe Herpes Simplex Virus Type 1 Amplicon Vector for Transcriptionally Targeted Therapy of Human Hepatocellular Carcinomas.

H. Huynh, K. S. Lim, P. Lam, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Matrix metalloproteinase‐1‐mediated mesenchymal stem cell tumor tropism is dependent on crosstalk with stromal derived growth factor 1/C‐X‐C chemokine receptor 4 axis

P. Lam, K. Hui, I. Ho, 2014, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Redox-Active Mn Porphyrin-based Potent SOD Mimic, MnTnBuOE-2-PyP5+, Enhances Carbenoxolone-Mediated TRAIL-Induced Apoptosis in Glioblastoma Multiforme

I. Batinic-Haberle, P. Lam, K. Hui, 2016, Stem Cell Reviews and Reports.

Targeting human glioma cells using HSV-1 amplicon peptide display vector

P. Lam, K. Hui, G. Wang, 2010, Gene Therapy.

Paracrine factors of human fetal MSCs inhibit liver cancer growth through reduced activation of IGF-1R/PI3K/Akt signaling.

H. Huynh, A. Chung, N. Iyer, 2015, Molecular therapy : the journal of the American Society of Gene Therapy.

An efficient and safe herpes simplex virus type 1 amplicon vector for transcriptionally targeted therapy of human hepatocellular carcinomas.

H. Huynh, K. S. Lim, P. Lam, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

The potential application of a transcriptionally regulated oncolytic herpes simplex virus for human cancer therapy

C. Fraefel, P. Lam, K. Sia, 2013, British Journal of Cancer.

Human mesenchymal stem cells preferentially migrate toward highly oncogenic human hepatocellular carcinoma cells with activated EpCAM signaling.

H. Huynh, A. Chung, K. Hui, 2017, Oncotarget.

Immunosuppression overcomes insulin- and vector-specific immune responses that limit efficacy of AAV2/8-mediated insulin gene therapy in NOD mice

A. Lever, A. Cooke, F. Reimann, 2018, Gene Therapy.

First use of gene therapy to treat growth hormone resistant dwarfism in a mouse model

M. Waters, J. Kopchick, S. Gan, 2022, Gene therapy.

Hybrid herpes simplex virus/Epstein–Barr virus amplicon viral vectors confer enhanced transgene expression in primary human tumors and human bone marrow‐derived mesenchymal stem cells

H. Huynh, P. Lam, I. Ho, 2010, The journal of gene medicine.

Suicidal gene therapy in the effective control of primary human hepatocellular carcinoma as monitored by noninvasive bioimaging

H. Huynh, P. Lam, K. Hui, 2012, Gene Therapy.

Optimal purification method for Herpes-based viral vectors that confers minimal cytotoxicity for systemic route of vector administration.

P. Lam, K. Hui, I. Ho, 2007, Journal of virological methods.

Combined treatment of Nimotuzumab and rapamycin is effective against temozolomide-resistant human gliomas regardless of the EGFR mutation status

P. Lam, X. Toh, D. Chong, 2015, BMC Cancer.

Combined treatment of Nimotuzumab and rapamycin is effective against temozolomide-resistant human gliomas regardless of the EGFR mutation status

P. Lam, X. Toh, D. Chong, 2015, BMC Cancer.

Preclinical Evaluation of Transcriptional Targeting Strategy for Human Hepatocellular Carcinoma in an Orthotopic Xenograft Mouse Model

H. Huynh, A. Chung, K. Hui, 2013, Molecular Cancer Therapeutics.

Redox-Active Mn Porphyrin-based Potent SOD Mimic, MnTnBuOE-2-PyP5+, Enhances Carbenoxolone-Mediated TRAIL-Induced Apoptosis in Glioblastoma Multiforme

I. Batinic-Haberle, P. Lam, K. Hui, 2016, Stem Cell Reviews and Reports.

Suicidal gene therapy in the effective control of primary human hepatocellular carcinoma as monitored by noninvasive bioimaging

H. Huynh, P. Lam, K. Hui, 2011, Gene Therapy.

Modification of a Constitutive to Glucose-Responsive Liver-Specific Promoter Resulted in Increased Efficacy of Adeno-Associated Virus Serotype 8-Insulin Gene Therapy of Diabetic Mice

R. Calne, A. Nathwani, S. Gan, 2020, Cells.

Development of a liver‐specific Tet‐off AAV8 vector for improved safety of insulin gene therapy for diabetes

R. Calne, O. Kon, S. Gan, 2019, The journal of gene medicine.

Engineering an improved cell cycle-regulatable herpes simplex virus type 1 amplicon vector with enhanced transgene expression in proliferating cells yet attenuated activities in resting cells.

P. Lam, K. Hui, I. Ho, 2007, Human gene therapy.

Efficient AAV9 Purification Using a Single-Step AAV9 Magnetic Affinity Beads Isolation

K. Sia, Zhenying Fu, Siti Humairah Mohd Rodhi, 2024, International Journal of Molecular Sciences.

Correction of Murine Diabetic Hyperglycaemia With A Single Systemic Administration of An AAV2/8 Vector Containing A Novel Codon Optimized Human Insulin Gene.

R. Calne, A. Nathwani, M. Notaridou, 2015, Current gene therapy.