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   Table of Contents
Coverpage
July-December 2015
Volume 2 | Issue 2
Page Nos. 1-198

Online since Wednesday, July 5, 2017

Accessed 19,918 times.

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GUEST EDITORIAL  

Can human embryos resulting from Somatic Cell Nuclear Transfers (SCNT) be used to treat human infertility? future implications in Assisted Reproductive Technologies (ART) p. 1
P Zavos
DOI:10.5530/ami.2015.2.1  
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GUEST EDITORIAL Top

Nanosurgery in metastatic breast cancer as postsurgical adjuvant treatment,targeted nanoimaging, and immunotargeted radiation therapy enhancement with nanomedicine p. 5
John N Giannios
DOI:10.5530/ami.2015.2.2  
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GUEST EDITORIAL Top

Morcellation Controversies p. 9
VG Hufnagel
DOI:10.5530/ami.2015.2.3  
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EDITORIAL Top

Why only Y-? p. 14
Sanjeev Kumar Jain, Nidhi Sharma, Rohin Garg
DOI:10.5530/ami.2015.2.4  
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ORIGINAL ARTICLE Top

Study about genetic variability of SE33 locus p. 16
A Barbaro, M Cassar, P Cormaci, JC Grech
DOI:10.5530/ami.2015.2.5  
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Association of CYP3A4*1B and CYP3A5*3 genetic polymorphisms with lung cancer and its impact on taxane metabolism in Indian population p. 19
Syed Subhani, Kaiser Jamil, Suresh Atilli
DOI:10.5530/ami.2015.2.6  
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MTHFR gene (C677t) polymorphism in Ischemic stroke, its subtypes and hemorrhagic stroke in a South Indian population p. 28
Satrupa Das, Sitara Roy, Subhash Kaul, Akka Jyothy, Anjana Munshi
DOI:10.5530/ami.2015.2.7  
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TPH2 variant rs7305115 and its interaction with acute stressful life events in etiology of suicide attempt in Serbian psychiatric patients p. 34
Jelena Karanovic, Maja Ivković, Maja Pantović, Goran Brajušković, Stanka Romac, Dušanka Savić Pavićević
DOI:10.5530/ami.2015.2.8  
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Two novel mutations in NKX 2.5 gene un-translated regions in congenital heart diseases patients from Pakistan p. 40
Afsheen Arif, Sitwat Zehra, Najma Patel, Abid Azhar
DOI:10.5530/ami.2015.2.9  
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Prognostic significance of ACE and PAI-1 genes polymorphisms with diabetic retinopathy and diabetic non-retinopathy in Type 2 diabetes p. 43
Sami Ullah Khan, Abdul Qayyum, Syed Sajjad Hussain
DOI:10.5530/ami.2015.3.0  
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HOXA9 gene expression and cytogenetic analysis in Egyptian acute myeloid leukemia patients p. 51
Hashem Neanaa, Nahla A. M Hamed, Ahmad Raafat, Iman Diab, Ahmed Abdel Rahman
DOI:10.5530/ami.2015.3.1  
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Histopathological and immunohistochemistry observations based bukhari grading for squamous cell carcinoma p. 54
Mulazim Hussain Bukhari, Kanwal Saba, Samina Qamar, Eyyaz Khalil, Shahida Niazi, Sardar Fakhar Imam
DOI:10.5530/ami.2015.3.2  
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Variation in growth pattern and morphological appearance of primary monolayer cultures of chondrocytes and neural cells isolated from the chick embryo at different stages p. 61
Rupendra Shrestha, Asha Palat, Selvam Anbarasan, Solomon F. D Paul
DOI:10.5530/ami.2015.3.3  
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Novel polymorphisms with in TLR4 exon1 sequences in visceral leishmaniasis and pulmonary tuberculosis patients p. 68
Hadeel Faisal Gad, Maowia M Mukhtar
DOI:10.5530/ami.2015.3.4  
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Cytoplasmic expression, optimization and catalytic activity evaluation of recombinant mature lysostaphin as an anti-staphylococcal therapeutic in escherichia coli p. 72
Samaneh Naderi, Mohammad Yousef Alikhani, Jamshid Karimi, Nooshin Shabab, Nejad Mohamadi, Hossein Zarei Jaliani, Massoud Saidijam
DOI:10.5530/ami.2015.3.5  
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Generation of a genetically engineered aggressive Nk-Cell leukemia cell line with stable IL2 expression p. 78
Xiaozhou Hu, Wing C Chan, Can Kűcűk
DOI:10.5530/ami.2015.3.6  
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Effect of elevated levels of hemoglobin F on HbA1c measurements: Evaluation of three HbA1c assays p. 85
A Khajuria, B Scheibe
DOI:10.5530/ami.2015.3.7  
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Evaluating the mRNA expression profile of APC in Pterygium p. 89
Maryam Najafi, Dor Mohammad Kordi-Tamandani, Mohammad Arish
DOI:10.5530/ami.2015.3.8  
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Detection of HPV and its association with different known risk factors for neoplastic cervical lesions p. 92
Kanwal Saba, Mulazim Hussain Bukhari, Eyyaz Khaleel, Sardar Fakhar Imam, Maidah Zainab, Abida Siddiqa, Ghayyor Ahmad, Ishtiaq Qadri, Muhammad Anwar
DOI:10.5530/ami.2015.3.9  
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Genetic counselling in anaemia & thalassemia p. 100
Jahnavi Hatti
DOI:10.5530/ami.2015.4.0  
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Prevalence of VKORC1 polymorphism in population of Hyderabad India p. 108
Amrita Rao, Gita Sharma, Livy Alex, R Tapadia
DOI:10.5530/ami.2015.4.1  
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REVIEW ARTICLE Top

Genetic and clinical aspects of brugada syndrome p. 112
Laila Anjuman Banu, Rifat Ara Najnin
DOI:10.5530/ami.2015.4.2  
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WHO recommended tools to improve diagnosis of active and drug resistant tuberculosis p. 118
Shubhada Shenai
DOI:10.5530/ami.2015.4.3  
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Genetics in psychiatry – diagnostic support or an illness classification! p. 130
Hena Jawaid, Syed Muhammad Ali
DOI:10.5530/ami.2015.4.4  
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Strategy planning for shortening the list of the metabolic syndrome candidate genes p. 135
MS Daneshpour
DOI:10.5530/ami.2015.4.5  
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Narrative review: Genetic findings in patients of generalized anxiety disorder p. 143
Aamir Abbas, Afshan Channa
DOI:10.5530/ami.2015.4.6  
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Current scenario on genetic basis of infertility- A review p. 149
Vishram Singh, Rohini Pakhiddey
DOI:10.5530/ami.2015.4.7  
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Gene therapy: A veracity or myth! p. 155
Sanjoy Kumar Chakraborty, Mahmudul Haque, Laila Anjuman Banu
DOI:10.5530/ami.2015.4.8  
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MSCs: Is this the future therapeutic for cancer? p. 161
Andrea Kakouri
DOI:10.5530/ami.2015.4.9  
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CASE REPORT Top

Fluorescence in situ hybridization on enriched CD138-positive cells in plasma cell myeloma p. 168
Yu Shi, Charalambos Solomides, Gerald Gong, Zi-Xuan (Zoe) Wang, GuldeepUppal , Vandi Ly, Stephen C Peiper, Peter A Herbut, Renu Bajaj
DOI:10.5530/ami.2015.5.0  
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Molecular cytogenetic characterization of a patient diagnosed with dimorphic anemia carrying de novo rare ring chromosome 7 along with T(7;9) p. 175
Saurabh Kumar Bhattacharya, Sumit Kumar, Jasbir Singh Bisht, Vandana Lal
DOI:10.5530/ami.2015.5.1  
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Quantifying environmental risk factors for multiple sclerosis in discordant monozygotic twins: A case report p. 178
Mohammad Reza Jabalameli, Seyed Amir Bahreini, Fereshteh Ashtari, Hamid Zahednasab
DOI:10.5530/ami.2015.5.2  
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Unusual involvement of the portal vein in polycythemia vera-genetic perspective p. 182
Tabinda Hasan, Erwa El Makki
DOI:10.5530/ami.2015.5.3  
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A 3-way rare variant Ph translocation t(7;9;22) in a patient with chronic myeloid leukemia p. 186
Saira Shan, Muhammad Nadeem, Tabbassum Ara, Tahir Shamsi
DOI:10.5530/ami.2015.5.4  
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A case of dic (1:15) (p11;p11) with t(9:22)(q34:q11) in B-ALL p. 189
Anitha Saminathan, Prabhu , Indhumathi Nagarathinam
DOI:10.5530/ami.2015.5.5  
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Tuberous sclerosis with bipolar disorder mania: Genetic perspective p. 191
Prerana Gupta, Jigar Haria
DOI:10.5530/ami.2015.5.6  
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SHORT COMMUNICATION Top

Thalassemia: Genetically transmitted blood disorder p. 195
Kausar Rehman Khan
DOI:10.5530/ami.2015.5.7  
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ORIGINAL ARTICLE Top

I have lynch syndrome p. 196
Georgia Hurst
DOI:10.5530/ami.2015.5.8  
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