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Akademický článek

Analysis of MNS16A VNTR polymorphic sequence variations of the TERT gene and associated risk for development of bladder cancer

Autor: Iqra Anwar, Arshad A. Pandith, Mohammad S. Wani, Hyder Mir, Meena Godha, Aabid Koul, Zafar A. Shah, Usma Manzoor, Ina Amin, Iqbal Qasim

Publikováno v: Current Urology, Vol 15, Iss 4, Pp 225-230 (2021)

Abstract. Background:. The MNS16A variable number tandem repeat (VNTR) polymorphism of the human telomerase reverse transcriptase (hTERT) gene acts as a regulator of hTERT promoter activity and has been shown to have a role in the predisposition towa

Externí odkaz: https://doaj.org/article/4e702752c980493b80e3cb4419c39638

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Prevalence and survival in patients with bladder cancer: a study in high cancer incidence zone

Autor: Iqra Anwar, Arshad A. Pandith, Mohammad S. Wani, Meena Godha, Usma Manzoor, Ina Amin, Aabid Koul

Publikováno v: Asian Pacific Journal of Health Sciences. 9:243-247

Background: Bladder cancer (BC) is the most common malignancy of the urinary tract caused by the uncontrollable division of cells lining the bladder. The clinicopathological characteristics of BC determine largely the prognosis and aid in the treatme

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eeeb9c4628f81ca37f3ecc820945ccaf
https://doi.org/10.21276/apjhs.2022.9.4.48

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Implications of VEGF gene sequence variations and its expression in recurrent pregnancy loss

Autor: Sheikh Mansoor, Iqra Anwar, Saima Wani, Aabid Koul, Umer Majeed Wani, Aabida Ahmad, Arshad A. Pandith, Iqbal Qasim, Qurat ul Aein, Usma Manzoor, Dil Afroze, Masarat Rashid, Syed Hussain Mir, Ina Amin

Publikováno v: Reproductive BioMedicine Online. 43:1035-1044

What is the association between VEGF gene sequence variants and its mRNA expression in recurrent pregnancy loss (RPL)? Vascular endothelial growth factor (VEGF) has a prominent role in pregnancy and affects pregnancy outcome. The association of VEGF

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df16dbe48c6c05d66fc87e09f9e2ea17
https://doi.org/10.1016/j.rbmo.2021.08.009

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High incidences of chromosomal aberrations and Y chromosome micro-deletions as prominent causes for recurrent pregnancy losses in highly ethnic and consanguineous population

Autor: Abida Ahmad, Shayesta Rah, Usma Manzoor, Iqbal Qasim, Ina Amin, Masarat Rashid, Dil-Afroze, Mahrukh H. Zargar, Dheera Sanadhya, Fayaz A Dar, Arshad A. Pandith

Publikováno v: Archives of Gynecology and Obstetrics. 305:1393-1408

Recurrent Miscarriages (RM) commonly complicates the reproductive outcome where prominently chromosomal aberrations and molecular factors lead to recurrent miscarriages. We investigated couples with RM for cytogenetic abnormalities and Y chromosome m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::18c901a8f5306f379009369bb52ed3f8
https://doi.org/10.1007/s00404-021-06235-z

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Analysis of MNS16A VNTR polymorphic sequence variations of the TERT gene and associated risk for development of bladder cancer

Autor: Zafar A. Shah, Aabid Koul, Arshad A. Pandith, Iqra Anwar, Meena Godha, Mohammad Saleem Wani, Iqbal Qasim, Usma Manzoor, Hyder Mir, Ina Amin

Publikováno v: Current Urology, Vol 15, Iss 4, Pp 225-230 (2021)

Background:. The MNS16A variable number tandem repeat (VNTR) polymorphism of the human telomerase reverse transcriptase (hTERT) gene acts as a regulator of hTERT promoter activity and has been shown to have a role in the predisposition toward various

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a737fb008a12588ce9591a9aa04c460
https://doi.org/10.1097/cu9.0000000000000040

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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

Autor: Usma Manzoor, Arshad A. Pandith, Ina Amin, Saima Wani, Dheera Sanadhya, Tawseef A. Lone, Hyder Mir, Bilal Ahamad Paray, Aneela Gulnaz, Iqra Anwar, Abida Ahmad, Qurat Ul Aein

Publikováno v: Journal of Clinical Medicine; Volume 11; Issue 13; Pages: 3834

Pregnancy is controlled by several types of genes and the regulation of their expression is tightly controlled by miRNAs. The present study was carried out to explore the association between miR-125a polymorphic sequence variation and its expression

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0390a8ea553b50344200b40ca8952619

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PREVALENCE AND IDENTIFICATION OF FLT3-ITD AND D835 ACTIVATING MUTATIONS IN ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) IN KASHMIRI PATIENTS (NORTH INDIA)

Autor: Iqra Anwar, Aabid Koul, Usma Manzoor, Javid Rasool, Sajad Geelani, Mithilesh Kumar, Ina Amin, Arshad A. Pandith, Fozia Mohammad

Publikováno v: International Journal of Advanced Research. 9:1324-1330

Background: The FLT3 gene, a receptor tyrosine kinase encodes a transmembrane protein that plays a fundamental role in normal hematopoiesis. The two types of mutations identified in FLT gene are an internal tandem duplication (FLT3-ITD) in exon 14 an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1a31653fdfc7f6bcb474545aa1d60ad6
https://doi.org/10.21474/ijar01/12975

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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)

Autor: Iqbal Qasim, Iqra Anwar, Arshad A. Pandith, Masarat Rashid, Saima Wani, Dheera Sanadhya, Abida Ahmad, Usma Manzoor, Ina Amin, Aabid Koul

Publikováno v: Journal of Obstetrics and Gynaecology Research. 47:1686-1693

AIM We aimed to evaluate the genetic variation of tumor necrosis factor-α (TNF-α) 308 G>A (rs1800629) and transforming growth factor (TGF) β1G>C (rs1800471) to confer risk in patients with recurrent miscarriage in highly consanguineous population

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::127129cce3056387f5731fd904944a80
https://doi.org/10.1111/jog.14718

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Influence of prominent immunomodulatory cytokines TNF-α308 GA (rs1800629) and TGFβ1 GC (rs1800471) sequence variations as an important contributing factor in etiopathogenesis of recurrent miscarriages in Kashmiri women (North India)

Autor: Usma, Manzoor, Arshad A, Pandith, Ina, Amin, Saima, Wani, Dheera, Sanadhya, Abida, Ahmad, Iqbal, Qasim, Masarat, Rashid, Iqra, Anwar, Aabid, Koul

Publikováno v: The journal of obstetrics and gynaecology researchReferences. 47(5)

We aimed to evaluate the genetic variation of tumor necrosis factor-α (TNF-α) 308 GA (rs1800629) and transforming growth factor (TGF) β1GC (rs1800471) to confer risk in patients with recurrent miscarriage in highly consanguineous population of Kas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fae65c34903630e104cab9c1485c88c6
https://pubmed.ncbi.nlm.nih.gov/33624323

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