Found: 26
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Glutathione S‐transferase gene polymorphic sequence variations: Association with risk and response to Imatinib among Chronic Myeloid Leukemia patients of Kashmir.
- Published in:
- International Journal of Laboratory Hematology, 2021, v. 43, n. 5, p. 1000, doi. 10.1111/ijlh.13471
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- Publication type:
- Article
Regulatory role of miR‐125a expression with respect to its target genes LIFR, ERBB2 and STAT3 in the pathogenesis of recurrent pregnancy losses.
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- International Journal of Gynecology & Obstetrics, 2024, v. 166, n. 3, p. 1285, doi. 10.1002/ijgo.15496
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- Publication type:
- Article
De novo Xp terminal deletion in a triple X female with recurrent spontaneous abortions: a case report
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- Journal of Genetics, 2014, v. 93, n. 3, p. 819, doi. 10.1007/s12041-014-0417-5
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- Publication type:
- Article
Influence of prominent immunomodulatory cytokines TNF‐α308 G>A (rs1800629) and TGFβ1 G>C (rs1800471) sequence variations as an important contributing factor in etiopathogenesis of recurrent miscarriages in Kashmiri women (North India).
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- Journal of Obstetrics & Gynaecology Research, 2021, v. 47, n. 5, p. 1686, doi. 10.1111/jog.14718
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- Publication type:
- Article
Significant Effect of Anti-tyrosine Kinase Inhibitor (Gefitinib) on Overall Survival of the Glioblastoma Multiforme Patients in the Backdrop of Mutational Status of Epidermal Growth Factor Receptor and PTEN Genes.
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- Asian Journal of Neurosurgery, 2018, v. 13, n. 1, p. 46, doi. 10.4103/ajns.AJNS_95_17
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- Article
Implications of risk conferred by 5p15.33 loci genetic variants; human telomerase reverse transcriptase rs2736098 and rs2736100 in predisposition of bladder cancer.
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- Reports of Practical Oncology & Radiotherapy, 2022, v. 27, n. 5, p. 787, doi. 10.5603/RPOR.a2022.0082
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- Article
Association of Bladder Cancer Risk with an NAD(P)H:Quinone Oxidoreductase Polymorphism in an Ethnic Kashmiri Population.
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- Biochemical Genetics, 2011, v. 49, n. 7/8, p. 417, doi. 10.1007/s10528-011-9418-8
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- Publication type:
- Article
Implications of Decreased Expression of miR-125a with Respect to Its Variant Allele in the Pathogenesis of Recurrent Pregnancy Loss: A Study in a High Incidence Zone.
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- Journal of Clinical Medicine, 2022, v. 11, n. 13, p. 3834, doi. 10.3390/jcm11133834
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- Publication type:
- Article
EPIDERMAL GROWTH FACTOR RECEPTOR (EGFR) POLYMORPHIC VARIATIONS (-216G/T & -191 C/A) POSE A HIGH RISK TO PATIENTS WITH MALIGNANT GLIOMA.
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- Experimental Oncology, 2023, v. 45, n. 2, p. 203, doi. 10.15407/exp-oncology.2023.02.203
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- Publication type:
- Article
High incidences of chromosomal aberrations and Y chromosome micro-deletions as prominent causes for recurrent pregnancy losses in highly ethnic and consanguineous population.
- Published in:
- Archives of Gynecology & Obstetrics, 2022, v. 305, n. 6, p. 1393, doi. 10.1007/s00404-021-06235-z
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- Publication type:
- Article
Significance and implications of FHIT gene expression and promoter hypermethylation in acute lymphoblastic leukemia (ALL).
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- Discover Oncology, 2024, v. 15, n. 1, p. 1, doi. 10.1007/s12672-024-00971-9
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- Publication type:
- Article
GSTT1 <sub>null</sub> and rs156697 Polymorphism in GSTO2 Influence the Risk and Therapeutic Outcome of B-Acute Lymphoblastic Leukemia Patients.
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- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.714421
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- Publication type:
- Article
Molecular Gate Keepers Succumb to Gene Aberrations in Colorectal Cancer in Kashmiri Population, Revealing a High Incidence Area.
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- Saudi Journal of Gastroenterology, 2009, v. 15, n. 4, p. 244, doi. 10.4103/1319-3767.56102
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- Publication type:
- Article
Possible Impact of RET Polymorphism and Its Haplotypic Association Modulates the Susceptibility to Thyroid Cancer.
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- Journal of Cellular Biochemistry, 2015, v. 116, n. 8, p. 1712, doi. 10.1002/jcb.25130
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- Article
Novelty of Axin 2 and lack of Axin 1 gene mutation in colorectal cancer: a study in Kashmiri population.
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- Molecular & Cellular Biochemistry, 2011, v. 355, n. 1/2, p. 149, doi. 10.1007/s11010-011-0848-8
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- Publication type:
- Article
Methylenetetrahydrofolate Reductase Gene C677T and A1298C Polymorphic Sequence Variations Influences the Susceptibility to Chronic Myeloid Leukemia in Kashmiri Population.
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- Frontiers in Oncology, 2019, p. 1, doi. 10.3389/fonc.2019.00612
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- Publication type:
- Article
Epigenetic silencing of TSHR gene in thyroid cancer patients in relation to their BRAF V600E mutation status.
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- Endocrine (1355008X), 2014, v. 47, n. 2, p. 449, doi. 10.1007/s12020-014-0319-6
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- Article
A Rare Case of FAP in Kashmir Valley.
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- 2011
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- Publication type:
- Report
Association of strong risk of hTERT gene polymorphic variants to malignant glioma and its prognostic implications with respect to different histological types and survival of glioma cases.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 11, p. 1, doi. 10.1002/jgm.3260
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- Publication type:
- Article
Impact of molecular alterations of BRAF in the pathogenesis of thyroid cancer.
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- Mutagenesis, 2014, v. 29, n. 2, p. 131, doi. 10.1093/mutage/get066
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- Publication type:
- Article
Significant Implications of APOA1 Gene Sequence Variations and Its Protein Expression in Bladder Cancer.
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- Biomedicines, 2021, v. 9, n. 8, p. 938, doi. 10.3390/biomedicines9080938
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- Publication type:
- Article
MGMT gene silencing by promoter hypermethylation in gastric cancer in a high incidence area.
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- Cellular Oncology (2211-3428), 2014, v. 37, n. 4, p. 245, doi. 10.1007/s13402-014-0179-3
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- Publication type:
- Article
Diversity of axin in signaling pathways and its relation to colorectal cancer.
- Published in:
- Medical Oncology, 2011, v. 28, p. 259, doi. 10.1007/s12032-010-9722-x
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- Publication type:
- Article
Association of APOA1-75G/A and +83C/T polymorphic variation with acute coronary syndrome patients in Kashmir (India).
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- Journal of Cardiovascular & Thoracic Research, 2021, v. 13, n. 2, p. 109, doi. 10.34172/jcvtr.2021.09
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- Publication type:
- Article
Cytogenetic diagnosis of Roberts SC phocomelia syndrome: First report from Kashmir.
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- 2016
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- Publication type:
- Case Study
Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India.
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- Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 1, p. 25, doi. 10.1016/j.ejmhg.2015.07.005
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- Publication type:
- Article