Items where Subject is "QZ Pathology"

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Number of items at this level: 126.

A

Abastabar, M. and Mirhendi, H. and Hedayati, M.T. and Shokohi, T. and Rezaei-Matehkolaei, A. and Mohammadi, R. and Badali, H. and Moazeni, M. and Haghani, I. and Ghojoghi, A. and Akhtari, J. (2016) Genetic and morphological diversity of the genus penicillium from mazandaran and tehran provinces, Iran. Jundishapur Journal of Microbiology, 9 (1).

Abbasi, B. and Nejad, N.A. and Fardad, F. and Nasiripour, S. and Ramim, T. (2016) Breast cancer epigenetics: Review article. Tehran University Medical Journal, 74 (8). pp. 535-544.

Afshar, R.M. and Mollaie, H.R. and Fazlalipour, M. and Arabzadeh, S.A. (2013) Prevalence and type distribution of human papillomavirus infection using the INNo-Lipa Assay, Kerman, Southeast Iran. Asian Pacific Journal of Cancer Prevention, 14 (9). pp. 5287-5291.

Aghaei, H. and Shahraki, K. (2013) Isolated cavernous hemangioma of the conjunctiva: Case report and review of literature. Iranian Journal of Ophthalmology, 25 (4). pp. 316-318.

Ahmadi, F. and Vahedpour, T. and Alizadeh, A.A. (2018) The evaluation of Cr-curcumin-DNA complexation by experimental and theoretical approaches. Nucleosides, Nucleotides and Nucleic Acids, 37 (1). pp. 35-52.

Alizadeh, F. and Bozorgmehr, A. and Tavakkoly-Bazzaz, J. and Ohadi, M. (2018) Skewing of the genetic architecture at the ZMYM3 human-specific 5� UTR short tandem repeat in schizophrenia. Molecular Genetics and Genomics, 293 (3). pp. 747-752.

Alizadeh, Z. and Mazinani, M. and Shakerian, L. and Nabavi, M. and Fazlollahi, M.R. (2018) DOCK2 Deficiency in a Patient with Hyper IgM Phenotype. Journal of Clinical Immunology, 38 (1). pp. 10-12.

Almasi, S. and Aslani, S. and Poormoghim, H. and Jamshidi, A. and Poursani, S. and Mahmoudi, M. (2016) Gene expression profiling of toll-like receptor 4 and 5 in peripheral blood mononuclear cells of patients with systemic sclerosis. American Journal of Immunology, 12 (1). pp. 10-16.

Amirian, A. and Dalili, S.M. and Zafari, Z. and Saber, S. and Karimipoor, M. and Akbari, V. and Fazelifar, A.F. and Zeinali, S. (2018) Novel frameshift mutation in the KCNQ1 gene responsible for jervell and lange-nielsen syndrome. Iranian Journal of Basic Medical Sciences, 21 (1). pp. 108-111.

Amirian, A. and Dalili, S.M. and Zafari, Z. and Saber, S. and Karimipoor, M. and Akbari, V. and Fazelifar, A.F. and Zeinali, S. (2018) Novel frameshift mutation in the KCNQ1 gene responsible for jervell and lange-nielsen syndrome. Iranian Journal of Basic Medical Sciences, 21 (1). pp. 108-111.

Ardebili, M.E. (2018) Transgenderism in Iran. UNSPECIFIED, pp. 158-165.

Asgari, F. and Falak, R. and Teimourian, S. and Pourakbari, B. and Ebrahimnezhad, S. and Shekarabi, M. (2018) Effects of oral probiotic feeding on toll-like receptor gene expression of the chicken's cecal tonsil. Reports of Biochemistry and Molecular Biology, 6 (2). pp. 151-157.

Atef-Vahid, M.-K. and Nasr-Esfahani, M. and Esfeedvajani, M.S. and Naji-Isfahani, H. and Shojaei, M.R. and Masoumeh Yasavoli, M. and Ashrafodin Goushegir, S. (2011) Quality of life, religious attitude and cancer coping in a sample of iranian patients with cancer. Journal of Research in Medical Sciences, 16 (7). pp. 928-937.

Attarchi, M.S. and Aminian, O. and Dolati, M. and Mazaheri, M. (2007) Evaluation of liver enzyme levels in workers exposed to vinyl chloride vapors in a petrochemical complex: A cross-sectional study. Journal of Occupational Medicine and Toxicology, 2 (1).

Azizi, G. and Bagheri, Y. and Yazdani, R. and Zaki-Dizaji, M. and Jamee, M. and Jadidi-Niaragh, F. and Kamali, A.N. and Abolhassani, H. and Aghamohammadi, A. (2018) The profile of IL-4, IL-5, IL-10 and GATA3 in patients with LRBA deficiency and CVID with no known monogenic disease: Association with disease severity. Allergologia et Immunopathologia.

B

Bademci, G. and Cengiz, F.B. and Foster, II and Duman, D. and Sennaroglu, L. and Diaz-Horta, O. and Atik, T. and Kirazli, T. and Olgun, L. and Alper, H. and Menendez, I. and Loclar, I. and Sennaroglu, G. and Tokgoz-Yilmaz, S. and Guo, S. and Olgun, Y. and Mahdieh, N. and Bonyadi, M. and Bozan, N. and Ayral, A. and Ozkinay, F. and Yildirim-Baylan, M. and Blanton, S.H. and Tekin, M. (2016) Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss. Scientific Reports, 6.

Bademci, G. and Foster, II and Mahdieh, N. and Bonyadi, M. and Duman, D. and Cengiz, F.B. and Menendez, I. and Diaz-Horta, O. and Shirkavand, A. and Zeinali, S. and Subasioglu, A. and Tokgoz-Yilmaz, S. and Huesca-Hernandez, F. and De La Luz Arenas-Sordo, M. and Dominguez-Aburto, J. and Hernandez-Zamora, E. and Montenegro, P. and Paredes, R. and Moreta, G. and Vinueza, R. and Villegas, F. and Mendoza-Benitez, S. and Guo, S. and Bozan, N. and Tos, T. and Incesulu, A. and Sennaroglu, G. and Blanton, S.H. and Ozturkmen-Akay, H. and Yildirim-Baylan, M. and Tekin, M. (2016) Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. Genetics in Medicine, 18 (4). pp. 364-371.

Bahador, M. and Keshtkar, M.M. and Zariee, A. (2018) Numerical and experimental investigation on the breast cancer tumour parameters by inverse heat transfer method using genetic algorithm and image processing. Sadhana - Academy Proceedings in Engineering Sciences, 43 (9).

Bahmani, N. and Hashemi, S.H. and Arabestani, M.R. and Mirnejad, R. and Masjedianjazi, F. and Keramat, F. and Alikhani, M.Y. (2018) Molecular typing of Brucella species isolated from humans and animals using polymerase chain reaction-restriction fragment length polymorphism technique. Archives of Clinical Infectious Diseases, 13 (2).

Bakhshi, B. and Ghafari, M. and Pourshafie, M.R. and Zarbakhsh, B. and Katouli, M. and Rahbar, M. and Hajia, M. and Hosseini-Aliabad, N. and Boustanshenas, M. (2015) Resistance-gene cassettes associated with Salmonella enterica genotypes. Laboratory Medicine, 46 (2). pp. 90-96.

Balali, M. and Kamalidehghan, B. and Farhadi, M. and Ahmadipour, F. and Ashkezari, M.D. and Hemami, M.R. and Arabzadeh, H. and Falah, M. and Meng, G.Y. and Houshmand, M. (2016) Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss. Therapeutics and Clinical Risk Management, 12. pp. 117-128.

Beik, J. and Mehdizadeh, A.R. and Shakeri-Zadeh, A. (2016) Ultrasound in cancer treatment through nanotechnology. Journal of Biomedical Physics and Engineering, 6 (3). pp. 123-126.

Bekloo, A.J. and Ramzgouyan, M.R. and Shirian, S. and Faghihi, F. and Bakhshi, H. and Naseri, F. and Sedaghat, M. and Telmadarraiy, Z. (2018) Molecular Characterization and Phylogenetic Analysis of Anaplasma spp. and Ehrlichia spp. Isolated from Various Ticks in Southeastern and Northwestern Regions of Iran. Vector-Borne and Zoonotic Diseases, 18 (5). pp. 252-257.

Bokharaei-Salim, F. and Salehi-Vaziri, M. and Sadeghi, F. and Esghaei, M. and Monavari, S.H. and Alavian, S.M. and Fakhim, S. and Keyvani, H. (2016) The association of substitutions in the hepatitis C virus subtype 1b core gene and IL28B polymorphisms with the response to peg-IFNα-2a/RBV combination therapy in Azerbaijani patients. Hepatitis Monthly, 16 (5).

Bordbar, A. and Maroofian, R. and Ostergaard, P. and Kashaki, M. and Nikpour, S. and Gordon, K. and Crosby, A. and Khosravi, P. and Shojaei, A. (2017) A homozygous loss-of-function mutation in PTPN14 causes a syndrome of bilateral choanal atresia and early infantile-onset lymphedema: PTPN14 mutation in lymphedema-choanal atresia. Meta Gene, 14. pp. 53-58.

Bozorgmehr, A. and Alizadeh, F. and Ofogh, S.N. and Hamzekalayi, M.R.A. and Herati, S. and Moradkhani, A. and Shahbazi, A. and Ghadirivasfi, M. (2018) What do the genetic association data say about the high risk of suicide in people with depression? A novel network-based approach to find common molecular basis for depression and suicidal behavior and related therapeutic targets. Journal of Affective Disorders, 229. pp. 463-468.

C

Cheki, M. and Yahyapour, R. and Farhood, B. and Rezaeyan, A. and Shabeeb, D. and Amini, P. and Rezapoor, S. and Najafi, M. (2018) COX-2 in radiotherapy: A potential target for radioprotection and radiosensitization. Current Molecular Pharmacology, 11 (3). pp. 173-183.

Cheraghi, M.A. and Rezasoltani, P. and Vedadhir, A. and Taghizadeh, Z. and Samadanifard, S.H. (2018) Parents� concerns regarding the growth characteristics of their adolescents: a qualitative inquiry in Iran. International Journal of Qualitative Studies on Health and Well-being, 13 (1).

D

Dai, F. and Yusuf, F. and Farjah, G.H. and Brand-Saberi, B. (2005) RNAi-induced targeted silencing of developmental control genes during chicken embryogenesis. Developmental Biology, 285 (1). pp. 80-90.

Davodian, E. and Sadeghifard, N. and Ghasemian, A. and Noorbakhsh, S. (2016) Presence of blaPER-1 and blaVEB-1 beta-lactamase genes among isolates of Pseudomonas aeruginosa from South West of Iran. Journal of Epidemiology and Global Health, 6 (3). pp. 211-213.

De Pagter, M.S. and Van Roosmalen, M.J. and Baas, A.F. and Renkens, I. and Duran, K.J. and Van Binsbergen, E. and Tavakoli-Yaraki, M. and Hochstenbach, R. and Van Der Veken, L.T. and Cuppen, E. and Kloosterman, W.P. (2015) Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring. American Journal of Human Genetics, 96 (4). pp. 651-656.

E

Entezam, M. and Razipour, M. and Talebi, S. and Beiraghi Toosi, M. and Keramatipour, M. (2018) Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation. Brain and Development.

Erfanian Saeedi, N. and Almasganj, F. and Torabinejad, F. (2011) Support vector wavelet adaptation for pathological voice assessment. Computers in Biology and Medicine, 41 (9). pp. 822-828.

Esfahani, B.N. and Moghim, S. and Safaei, H.G. and Moghoofei, M. and Sedighi, M. and Hadifar, S. (2016) Phylogenetic analysis of prevalent tuberculosis and non-Tuberculosis Mycobacteria in Isfahan, Iran, based on a 360 bp sequence of the rpoB gene. Jundishapur Journal of Microbiology, 9 (4).

Estiri, H. and Fallah, A. and Soleimani, M. and Aliaghaei, A. and Karimzadeh, F. and Abraki, S.B. and Ghahremani, M.H. (2018) Stable Knockdown of Adenosine Kinase by Lentiviral Anti-ADK miR-shRNAs in Wharton�s Jelly Stem Cells. Cell Journal, 20 (1). pp. 1-9.

F

Falah, M. and Houshmand, M. and Najafi, M. and Balali, M. and Mahmoudian, S. and Asghari, A. and Emamdjomeh, H. and Farhadi, M. (2016) The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis. Therapeutics and Clinical Risk Management, 12. pp. 1573-1578.

Falah, M. and Najafi, M. and Houshmand, M. and Farhadi, M. (2016) Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment. Clinical Interventions in Aging, 11. pp. 1003-1008.

Fanuel, S. and Tabesh, S. and Mokhtarian, K. and Saroddiny, E. and Fazlollahi, M.R. and Pourpak, Z. and Falak, R. and Kardar, G.A. (2018) Construction of a recombinant B-cell epitope vaccine based on a der p1-derived hypoallergen: A bioinformatics approach. Immunotherapy, 10 (7). pp. 537-553.

Farjadian, F. and Moghoofei, M. and Mirkiani, S. and Ghasemi, A. and Rabiee, N. and Hadifar, S. and Beyzavi, A. and Karimi, M. and Hamblin, M.R. (2018) Bacterial components as naturally inspired nano-carriers for drug/gene delivery and immunization: Set the bugs to work? Biotechnology Advances, 36 (4). pp. 968-985.

Fateminasab, F.-D. and Shahgasempour, S. and Mirsaeidi, S.-M. and Tabarsi, P. and Mansoori, S.-D. and Entezami, Z. (2006) Increased activation and expansion of a CD57+ subset within peripheral CD8+ T lymphocytes in mycobacterium tuberculosis-infected patients. Archives of Iranian Medicine, 9 (1). pp. 53-57.

Fattahi, A. and Jahanbakhshi, A. and Shahivand, A. and Dastmalchi, A. (2018) Penetrating Sacral Injury with a Wooden Foreign Body. Case Reports in Medicine, 2018.

Fattahi, A. and Zaini, F. and Kordbacheh, P. and Rezaie, S. and Safara, M. and Fateh, R. and Farahyar, S. and Kanani, A. and Heidari, M. (2015) Evaluation of mRNA expression levels of cyp51a and mdr1, candidate genes for voriconazole resistance in Aspergillus flavus. Jundishapur Journal of Microbiology, 8 (12).

Fattahi-Dolatabadi, M. and Mousavi, T. and Mohammadi-Barzelighi, H. and Irian, S. and Bakhshi, B. and Nilforoushzadeh, M.-A. and Shirani-Bidabadi, L. and Hariri, M.-M. and Ansari, N. and Akbari, N. (2016) NRAMP1 gene polymorphisms and cutaneous leishmaniasis: An evaluation on host susceptibility and treatment outcome. Journal of Vector Borne Diseases, 53 (3). pp. 257-263.

Fazeli, Gh.R. and Khoei, S. and Nikoofar, A.R. and Goliaei, B. (2007) Reduced DNA damage in tumor spheroids compared to monolayer cultures exposed to ionizing radiation. Iranian Journal of Radiation Research, 5 (2). pp. 63-69.

Fazilaty, H. and Gardaneh, M. and Bahrami, T. and Salmaninejad, A. and Behnam, B. (2013) Crosstalk between breast cancer stem cells and metastatic niche: Emerging molecular metastasis pathway? Tumor Biology, 34 (4). pp. 2019-2030.

Fazilaty, Z. and Chenari, H. and Shariatpanahi, Z.V. (2018) Effect of β-glucan on serum levels of IL-12, hs-CRP, and clinical outcomes in multiple-trauma patients: A prospective randomized study �oklu travma hastalarda β �glukanın serum IL-12, hs-CRP de�erleri ve klinik sonuçları üzerine etkisi: Ileriye yönelik randomize çalı�ma. Ulusal Travma ve Acil Cerrahi Dergisi, 24 (4). pp. 287-293.

Fitzmaurice, C. and Dicker, D. and Pain, A. and Hamavid, H. and Moradi-Lakeh, M. and MacIntyre, M.F. and Allen, C. and Hansen, G. and Woodbrook, R. and Wolfe, C. and Hamadeh, R.R. and Moore, A. and Werdecker, A. and Gessner, B.D. and Te Ao, B. and McMahon, B. and Karimkhani, C. and Yu, C. and Cooke, G.S. and Schwebel, D.C. and Carpenter, D.O. and Pereira, D.M. and Nash, D. and Kazi, D.S. and De Leo, D. and Plass, D. and Ukwaja, K.N. and Thurston, G.D. and Yun Jin, K. and Simard, E.P. and Mills, E. and Park, E.-K. and Catalá-López, F. and DeVeber, G. and Gotay, C. and Khan, G. and Hosgood, III and Santos, I.S. and Leasher, J.L. and Singh, J. and Leigh, J. and Jonas, J.B. and Sanabria, J. and Beardsley, J. and Jacobsen, K.H. and Takahashi, K. and Franklin, R.C. and Ronfani, L. and Montico, M. and Naldi, L. and Tonelli, M. and Geleijnse, J. and Petzold, M. and Shrime, M.G. and Younis, M. and Yonemoto, N. and Breitborde, N. and Yip, P. and Pourmalek, F. and Lotufo, P.A. and Esteghamati, A. and Hankey, G.J. and Ali, R. and Lunevicius, R. and Malekzadeh, R. and Dellavalle, R. and Weintraub, R. and Lucas, R. and Hay, R. and Rojas-Rueda, D. and Westerman, R. and Sepanlou, S.G. and Nolte, S. and Patten, S. and Weichenthal, S. and Abera, S.F. and Fereshtehnejad, S.-M. and Shiue, I. and Driscoll, T. and Vasankari, T. and Alsharif, U. and Rahimi-Movaghar, V. and Vlassov, V.V. and Marcenes, W.S. and Mekonnen, W. and Melaku, Y.A. and Yano, Y. and Artaman, A. and Campos, I. and MacLachlan, J. and Mueller, U. and Kim, D. and Trillini, M. and Eshrati, B. and Williams, H.C. and Shibuya, K. and Dandona, R. and Murthy, K. and Cowie, B. and Amare, A.T. and Antonio, C.A. and Castañeda-Orjuela, C. and Van Gool, C.H. and Violante, F. and Oh, I.-H. and Deribe, K. and Soreide, K. and Knibbs, L. and Kereselidze, M. and Green, M. and Cardenas, R. and Roy, N. and Tillmann, T. and Li, Y. and Krueger, H. and Monasta, L. and Dey, S. and Sheikhbahaei, S. and Hafezi-Nejad, N. and Kumar, G.A. and Sreeramareddy, C.T. and Dandona, L. and Wang, H. and Vollset, S.E. and Mokdad, A. and Salomon, J.A. and Lozano, R. and Vos, T. and Forouzanfar, M. and Lopez, A. and Murray, C. and Naghavi, M. (2015) The Global Burden of Cancer 2013. JAMA Oncology, 1 (4). pp. 505-527.

G

Gelyan, H.N. and Makhdumi, Y. and Nikoofar, A. and Hasanzadeh, H. (2016) Measurement of surface dose in external radiotherapy of brain frontal lobe: A study on patient and phantom. Koomesh, 17 (2). pp. 323-328.

Ghazi, A.A. and Boustani, I. and Amouzegar, A. and Attarian, H. and Pourafkari, M. and Gashti, H.N. and Sabetian, T. and Tirgari, F. and Ghazi, S. and Kovacs, K. (2011) Postpartum hypercalcemia secondary to a neuroendocrine tumor of pancreas; a case report and review of literature. Iranian Journal of Medical Sciences, 36 (3). pp. 217-221.

Golalipour, M.J. and Kaviany, N. and Golalipour, E. and Mirfazeli, A. and Behnampour, N. (2018) Prevalence and patterns of congenital limb defects in the north of Iran (2007-2011). Iranian Journal of Neonatology, 9 (1). pp. 60-64.

Goradel, N.H. and Ghiyami-Hour, F. and Jahangiri, S. and Negahdari, B. and Sahebkar, A. and Masoudifar, A. and Mirzaei, H. (2018) Nanoparticles as new tools for inhibition of cancer angiogenesis. Journal of Cellular Physiology, 233 (4). pp. 2902-2910.

Goudarzi, F. and Mohammadalipour, A. and Bahabadi, M. and Moradi, M.N. and Sarve-Azad, A. and Goodarzi, M.T. and Khodadadi, I. (2018) The ability of H2O2 to induce differentiation of human mesenchymal stem cells into chondrocytes. Scientific Journal of Kurdistan University of Medical Sciences, 22 (6). pp. 63-73.

H

Hadji, M. and Nahvijou, A. and Seddighi, Z. and Beiki, O. and Mohagheghi, M.A. and Mosavi-Jarrahi, A. and Marnani, A.B. and Zendehdel, K. (2013) Challenges to promoting population-based cancer registration in Iran: A workshop report. Asian Pacific Journal of Cancer Prevention, 14 (10). pp. 6189-6193.

Hosseini, S. and Kalantar, E. and Hosseini, M.S. and Tabibian, S. and Shamsizadeh, M. and Dorgalaleh, A. (2015) Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population. Thrombosis Journal, 13 (1).

Hosseini-Fard, S.R. and Mohammadi, A. and Naiafi, M. and Shabani, M. and Javedan, G. (2016) Relationship Between Sterol Regulatory Element- Binding Protein-2 Gene Expression Level and Lipid Profile. Journal of Mazandaran University of Medical Sciences, 26 (140). pp. 24-32.

I

Izadi, F. and Mahjoubi, F. and Farhadi, M. and Kalayinia, S. and Bidmeshkipour, A. and Tavakoli, M.M. and Samanian, S. (2016) Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosis. Indian Journal of Medical Research, 143 (MARCH). pp. 303-307.

J

Jafaryazdi, R. and Shams, S. and Isaian, A. and Ebadi, E. and Safaralizadeh, R. and Teimourian, S. (2018) A novel compound heterozygote mutation in the ARSB gene in a patient with Maroteaux-Lamy syndrome and its Insilico evaluation. Meta Gene, 18. pp. 127-131.

Jalilian, N. and Tabatabaiefar, M.A. and Yazdanpanah, M. and Darabi, E. and Bahrami, T. and Zekri, A. and Noori-Daloii, M.R. (2018) A comprehensive genetic and clinical evaluation of Waardenburg syndrome type II in a set of Iranian patients. International Journal of Molecular and Cellular Medicine, 7 (1).

Jamilian, M. and Samimi, M. and Mirhosseini, N. and Afshar Ebrahimi, F. and Aghadavod, E. and Talaee, R. and Jafarnejad, S. and Hashemi Dizaji, S. and Asemi, Z. (2018) The influences of vitamin D and omega-3 co-supplementation on clinical, metabolic and genetic parameters in women with polycystic ovary syndrome. Journal of Affective Disorders, 238. pp. 32-38.

Javaheri, D. and Hosseinzadeh, M. (2018) A Framework for Recognition and Confronting of Obfuscated Malwares Based on Memory Dumping and Filter Drivers. Wireless Personal Communications, 98 (1). pp. 119-137.

K

Kadivar, M. and Joulaee, A. and Kashkouli, M.B. and Kharazi, H.H. and Kalantari, M. and Kumar, P.V. (2006) Orbital metastasis as the first presentation of nonpalpable invasive lobular carcinoma of the breast. Breast Journal, 12 (1). pp. 75-76.

Kanani, A. and Zaini, F. and Kordbacheh, P. and Falahati, M. and Rezaie, S. and Daie, R. and Farahyar, S. and Safara, M. and Fateh, R. and Faghihloo, E. and Fattahi, A. and Heidari, M. (2016) Identification of Azole Resistance Markers in Clinical Isolates of Candida tropicalis Using cDNA-AFLP Method. Journal of Clinical Laboratory Analysis, 30 (3). pp. 266-272.

Kaveh, M.H. and Darabi, F. and Khalajabadi-Farahani, F. and Yaseri, M. and Mohammadi, M.J. and Behrooz, H.R.A. and Shojaeizadeh, D. and Rohban, A. (2018) The impact of a TPB-based educational intervention on nutritional behaviors in Iranian adolescent Girls: A randomized controlled trial. Fresenius Environmental Bulletin, 27 (6). pp. 4349-4356.

Kazemi, M. and Nazari, B. and Ai, J. and Lotfibakhshaiesh, N. and Samadikuchaksaraei, A. and Tavangar, S.M. and Azami, M. (2018) Preparation and characterization of highly porous ceramic-based nanocomposite scaffolds with improved mechanical properties using the liquid phase-assisted sintering method. Proceedings of the Institution of Mechanical Engineers, Part L: Journal of Materials: Design and Applications.

Keshavarz, M. and Moloudi, K. and Paydar, R. and Abed, Z. and Beik, J. and Ghaznavi, H. and Shakeri-Zadeh, A. (2018) Alginate hydrogel co-loaded with cisplatin and gold nanoparticles for computed tomography image-guided chemotherapy. Journal of Biomaterials Applications, 33 (2). pp. 161-169.

Keymoosi, H. and Gheytanchi, E. and Asgari, M. and Shariftabrizi, A. and Madjd, Z. ALDH1 in combination with CD44 as putative cancer stem cell markers are correlated with poor prognosis in urothelial carcinoma of the urinary bladder. Asian Pacific Journal of Cancer Prevention, 15 (5). pp. 2013-2020. ISSN 1513-7368

Khanjari, S. and Oskouie, F. and Langius-Eklöf, A. (2012) Psychometric testing of the Caregiver Quality of Life Index-Cancer scale in an Iranian sample of family caregivers to newly diagnosed breast cancer women. Journal of Clinical Nursing, 21 (3-4). pp. 573-584.

Koohpar, Z.K. and Entezari, M. and Movafagh, A. and Hashemi, M. (2015) Anticancer activity of curcumin on human breast adenocarcinoma: Role of Mcl-1 gene. International Journal of Cancer Management, 8 (3).

L

Lam, W.S.-T. and Wang, L.Z. and Roudi, R. and Yong, W.-P. and Syn, N.L. and Sundar, R. (2018) Resisting resistance to cancer immunotherapy. Thoracic Cancer, 9 (5). pp. 507-508.

Lari, A.R. and Ardebili, A. and Hashemi, A. (2018) Ader-ades mutations & overexpression of the AdeABC efflux system in ciprofloxacin-resistant acinetobacter baumannii clinical isolates. Indian Journal of Medical Research, 147 (April). pp. 413-421.

Larijani, L. and Madjd, Z. and Samadikuchaksaraei, A. and Younespour, S. and Zham, H. and Rakhshan, A. and Mohammadi, F. and Rahbari, A. and Moradi, A. (2014) Methylation of O6-methyl guanine methyltransferase gene promoter in meningiomas - comparison between tumor grades I, II, and III. Asian Pacific Journal of Cancer Prevention, 15 (1). pp. 33-38.

M

Madani, T. and Ashrafi, M. and Yeganeh, L.M. (2012) Comparison of different stimulation protocols efficacy in poor responders undergoing IVF: A retrospective study. Gynecological Endocrinology, 28 (2). pp. 102-105.

Madjd, Z. and Gheytanchi, E. and Erfani, E. and Asadi-Lari, M. (2013) Application of stem cells in targeted therapy of breast cancer: A systematic review. Asian Pacific Journal of Cancer Prevention, 14 (5). pp. 2789-2800.

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This list was generated on Sun Dec 15 00:38:53 2019 +0330.