Associated Papers
Systems-Level Integration of Multi-Omics Identifies Genetic Modifiers of TANGO2 Deficiency Disorder.
Airoldi M et al.
Biomolecules, 2025
Association of genotypes at single-nucleotide polymorphisms in IL-28B, TGF-β1, TP53, MTHFR and GSTP1 gene and their combinations with ischemic stroke: A case-control study.
Shakoor S et al.
Ibro Neuroscience Reports, 2025
Understanding genetic variations associated with familial breast cancer.
Pal M et al.
World Journal of Surgical Oncology, 2024
Association between fibrosis-related gene polymorphism and long-term allograft outcome in renal transplant recipients.
Yin Y et al.
Bmc Medical Genomics, 2023
Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertension.
van Duijvenboden S et al.
American Journal of Human Genetics, 2023
Genetic variations in idiopathic pulmonary fibrosis and patient response to pirfenidone.
Kubbara A et al.
Heliyon, 2023
Genetic Risk Factors Related to Coronary Artery Disease and Role of Transforming Growth Factor Beta 1 Polymorphisms.
Malinowski D et al.
Genes, 2023
Association Study of Transforming Growth Factor Beta 1 + 29 T/C exon 1 Polymorphism in Breast Cancer Patients from North Indian Population.
Pal R et al.
Applied Biochemistry and Biotechnology, 2023
Comparative analysis of histopathological parameters, genome-wide copy number alterations, and variants in genes involved in cell cycle regulation in chordomas of the skull base and sacrum.
Salle H et al.
Journal of Neuropathology and Experimental Neurology, 2023
TGF-β1 and TGFβR2 Gene Polymorphisms in Patients with Unstable Angina.
Malinowski D et al.
Biomedicines, 2023
Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.
Boukhalfa W et al.
Frontiers in Aging Neuroscience, 2023
Genetic Polymorphisms Involved in Bladder Cancer: A Global Review.
Kourie HR et al.
Oncology Reviews, 2023
Role of TGF-β1 +869T>C polymorphism in renal dysfunction one year after heart transplantation.
López-Ibor JV et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation, 2022
Genetic susceptibility of bladder cancer in the Lebanese population.
Kourie HR et al.
Bmc Medical Genomics, 2022
Case-Control Genotyping of the c.788C>T Variant of Transforming Growth Factor-Beta 1 Gene in Otosclerosis in the South Indian Population.
Kale D et al.
The Journal of International Advanced Otology, 2022
Manipulation of Interleukin-6 (IL-6) and Transforming Growth Factor Beta-1(TGFβ-1) towards viral induced liver cancer pathogenesis.
Badshah Y et al.
Plos One, 2022
Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease.
Liang H et al.
Frontiers in Endocrinology, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Genetic markers of osteoarthritis: early diagnosis in susceptible Pakistani population.
Badshah Y et al.
Journal of Orthopaedic Surgery and Research, 2021
Genetic Polymorphisms of the TGFB1 Signal Peptide and Promoter Region: Role in Wilms Tumor Susceptibility?
Ishibashi CM et al.
Journal of Kidney Cancer and Vhl, 2021
The Association of Interleukin-6 (IL-6) -572G/C and Transforming Growth Factor Beta 1 (TGFB1) 29C/T Single Nucleotide Polymorphisms (SNPs) with Developmental Dysplasia of the Hip: a Case Control Study.
İğrek S et al.
Acta Chirurgiae Orthopaedicae Et Traumatologiae Cechoslovaca, 2021
A Systematic Review and Meta-Analysis on Multiple Cytokine Gene Polymorphisms in the Pathogenesis of Periodontitis.
Liu X et al.
Frontiers in Immunology, 2021
Effect of functional variant rs11466313 on breast cancer susceptibility and TGFB1 promoter activity.
Zhou YT et al.
Breast Cancer Research and Treatment, 2020
Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa.
Jurj MA et al.
International Journal of Molecular Sciences, 2020
Transforming growth factor beta 1 (TGFβ1) polymorphisms and unexplained infertility: A genetic association study.
Marhemati F et al.
Systems Biology in Reproductive Medicine, 2020
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population.
Corredor Z et al.
Scientific Reports, 2020
TGF-β and microRNA Interplay in Genitourinary Cancers.
Boguslawska J et al.
Cells, 2019
A Single-Nucleotide Polymorphism (rs1131243) of the Transforming Growth Factor Beta Signaling Pathway Contributes to Risk of Acute Rejection in Chinese Renal Transplant Recipients.
Zheng M et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2019
Introducing the first whole genomes of nationals from the United Arab Emirates.
AlSafar HS et al.
Scientific Reports, 2019
Transforming growth factor beta 1 polymorphisms and haplotypes associated with breast cancer susceptibility: A case-control study in Tunisian women.
Hadj-Ahmed M et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2019
MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip.
Gajera M et al.
Bmc Medical Genomics, 2019
EGFR, SMAD7, and TGFBR2 Polymorphisms Are Associated with Colorectal Cancer in Patients with Lynch Syndrome.
Kamiza AB et al.
Anticancer Research, 2018
Transforming growth factor beta 1 (TGFβ1) polymorphisms and haplotype structures have dual roles in breast cancer pathogenesis.
Vitiello GAF et al.
Journal of Cancer Research and Clinical Oncology, 2018
Association between Altered Expression and Genetic Variations of Transforming Growth Factor β-Smad Pathway with Chronic Myeloid Leukemia.
Shokeen Y et al.
International Journal of Hematology-oncology and Stem Cell Research, 2018
The c.29T>C polymorphism of the transforming growth factor beta-1 (TGFB1) gene, bone mineral density and the occurrence of low-energy fractures in patients with inflammatory bowel disease.
Krela-Kaźmierczak I et al.
Molecular Biology Reports, 2017
Transforming growth factor-β1 functional polymorphisms in myeloablative sibling hematopoietic stem cell transplantation.
Berro M et al.
Bone Marrow Transplantation, 2017
Lack of association between genotype score and sprint/power performance in the Japanese population.
Miyamoto-Mikami E et al.
Journal of Science and Medicine in Sport, 2017
Clinical diagnosis and mutation analysis of a Chinese family with Camurati-Engelmann disease.
Chen Y et al.
Molecular Medicine Reports, 2017
Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.
Raaijmakers MI et al.
Oncotarget, 2016