日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Implications of lipoprotein (a) [Lp(a)] gene polymorphic sequence variations and its protein expression in venous thromboembolism (VTE)

脂蛋白(a) [Lp(a)] 基因多态性序列变异及其蛋白表达在静脉血栓栓塞症 (VTE) 中的意义

Happa, Karan; Pandith, Arshad A; Khan, Umar H; Rasool, Shayaq Ul Abeer; Koul, Aabid M; Ain, Qurat Ul; Uzair Ul Haq, Mir; Manzoor, Usma; Lateef, Adil; Jan, Rafi A

Polymorphic Variants of FOXP3 Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India)

FOXP3基因的多态性变异(rs 3761548)和(rs 3761549)与复发性流产的风险显著相关。一项在高发地区(印度北部克什米尔)进行的研究证实了这一点。

Manzoor, Usma; Pandith, Arshad A; Lone, Tawseef A; Hameed, Amreena; Nisa, Falak U; Amin, Ina; Rah, Shayesta; Wani, Saima; Rasool, Shayaq Ul Abeer; Lateef, Adil; Ahmad, Aabida

Significance and implications of FHIT gene expression and promoter hypermethylation in acute lymphoblastic leukemia (ALL)

FHIT基因表达和启动子高甲基化在急性淋巴细胞白血病(ALL)中的意义和影响

Mohammad, Fozia; Pandith, Arshad A; Rasool, Shayaq Ul Abeer; Guru, Faisal R; Qasim, Iqbal; Geelani, Sajad; Nisar, Syed; Baba, Shahid M; Ganie, Farooq A; Kouser, Safiya; Rasool, Javid

Significant Implications of APOA1 Gene Sequence Variations and Its Protein Expression in Bladder Cancer

APOA1基因序列变异及其蛋白表达在膀胱癌中的重要意义

Magray, Javid A; Pandith, Arshad A; Qasim, Iqbal; Khateeb, Muzzain; Hamid, Arif; Koul, Aabid; Shah, Zafar A; Baba, Shahid M; Mansoor, Sheikh; Charifi, Wafa; Ahmad, Ajaz; Wani, Mohammad S

GSTT1 (null) and rs156697 Polymorphism in GSTO2 Influence the Risk and Therapeutic Outcome of B-Acute Lymphoblastic Leukemia Patients.

GSTT1(null)和 rs156697 多态性在 GSTO2 中影响 B 急性淋巴细胞白血病患者的风险和治疗结果

Baba Shahid M, Pandith Arshad A, Shah Zafar A, Geelani Sajad A, Bhat Javid R, Gul Ayaz, Guru Sameer A, El-Serehy Hamed A, Koul Abid M, Mansoor Sheikh

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

分析TERT基因MNS16A VNTR多态性序列变异及其与膀胱癌发生风险的相关性

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

Impact of ABCB1 Gene (C3435T/A2677G) Polymorphic Sequence Variations on the Outcome of Patients with Chronic Myeloid Leukemia and Acute Lymphoblastic Leukemia in Kashmiri Population: A Case-Control Study.

ABCB1 基因 (C3435T/A2677G) 多态性序列变异对克什米尔人群慢性粒细胞白血病和急性淋巴细胞白血病患者预后的影响:一项病例对照研究

Baba Shahid M, Pandith Arshad A, Shah Zafar A, Geelani Sajad A, Mir Mohammad Muzaffar, Bhat Javid Rasool, Bhat Gul Mohammad

Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma

IDH1/2突变与MGMT启动子基因甲基化在恶性胶质瘤患者预后中发挥有利作用

Pandith, Arshad A; Qasim, Iqbal; Baba, Shahid M; Koul, Aabid; Zahoor, Wani; Afroze, Dil; Lateef, Adil; Manzoor, Usma; Bhat, Ina A; Sanadhya, Dheera; Bhat, Abdul R; Ramzan, Altaf U; Mohammad, Fozia; Anwar, Iqra

Methylenetetrahydrofolate Reductase Gene C677T and A1298C Polymorphic Sequence Variations Influences the Susceptibility to Chronic Myeloid Leukemia in Kashmiri Population.

亚甲基四氢叶酸还原酶基因 C677T 和 A1298C 多态性序列变异影响克什米尔人群对慢性粒细胞白血病的易感性

Baba Shahid M, Shah Zafar A, Javaid Khushboo, Pandith Arshad A, Rasool Javeed, Geelani Sajad A, Baba Rafia A, Amin Shajrul, Mohammad Gul

Real-time quantitative PCR: a reliable molecular diagnostic and follow-up tool for 'minimal residual disease' assessment in chronic myeloid leukemia

实时定量PCR:一种可靠的分子诊断和随访工具,用于评估慢性粒细胞白血病中的“微小残留病灶”。

Azad, Niyaz A; Shah, Zafar A; Pandith, Arshad A; Rasool, Roohi; Jeelani, Samoon