Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ina Amin"'
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
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
https://doi.org/10.21276/apjhs.2022.9.4.48
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
https://doi.org/10.1016/j.rbmo.2021.08.009
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
https://doi.org/10.1007/s00404-021-06235-z
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
https://doi.org/10.1097/cu9.0000000000000040
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
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
https://doi.org/10.21474/ijar01/12975
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
https://doi.org/10.1111/jog.14718
Autor:
Iqra Anwar, Arshad A. Pandith, Hyder Mir, Usma Manzoor, Ina Amin, Shahid M. Baba, Meena Godha, Aabid M. Koul, Zafar A. Shah, Sheikh Mansoor, Mohammad S. Wani
Publikováno v:
Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology. 27(5)
The polymorphic variations of human telomerase reverse transcriptase (Confirmed 130 patients of bladder cancer and 200 healthy controls were genotyped by PCR-RFLP to determine different variants ofIt is concluded that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71bca37f8b18003526f810c2ae7e64e3
https://pubmed.ncbi.nlm.nih.gov/36523804
https://pubmed.ncbi.nlm.nih.gov/36523804
Autor:
Sheikh Mansoor, Usma Manzoor, Aabid Mustafa Koul, Shahid M. Baba, Ina Amin, Iqra Anwar, Qurat ul Aein, Arshad A. Pandith
Publikováno v:
Breast Cancer: From Bench to Personalized Medicine ISBN: 9789811901966
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5899f1fa3459e37fa6459e835b72786c
https://doi.org/10.1007/978-981-19-0197-3_5
https://doi.org/10.1007/978-981-19-0197-3_5
