Massoud HOUSHMAND: search on Z-Library

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1

Ancient Migratory Events in the Middle East: New Clues from the Y-Chromosome Variation of Modern Iranians

Grugni, Viola, Battaglia, Vincenza, Hooshiar Kashani, Baharak, Parolo, Silvia, Al-Zahery, Nadia, Achilli, Alessandro, Olivieri, Anna, Gandini, Francesca, Houshmand, Massoud, Sanati, Mohammad Hossein,

Journal:

Year:

2012

Language:

english

File:

PDF, 1.60 MB

english, 2012

2

Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C

Masserrat, Abbas, Sharifpanah, Fatemeh, Akbari, Leila, Tonekaboni, Seyed, Karimzadeh, Parvaneh, Asharafi, Mahmood Reza, Mazouei, Safoura, Sauer, Heinrich, Houshmand, Massoud

Journal:

Biomedical Reports

Year:

2018

Language:

english

File:

PDF, 479 KB

english, 2018

3

Genipin induces cell death via intrinsic apoptosis pathways in human glioblastoma cells

Ahani, Narges, Sangtarash, Mohammad Hossein, Houshmand, Massoud, Eskandani, Majid Alipour

Journal:

Journal of Cellular Biochemistry

Year:

2018

Language:

english

File:

PDF, 1.06 MB

english, 2018

4

Mitochondrial DNA sequence diversity in three ethnic populations from the South-west Iran: a preliminary study

Elham Davoudi-Dehaghani, Ali Mohammad Foroughmand, Babak Saffari, Massoud Houshmand, Hamid Galehdari, Mehdi Shafa Shariat Panahi, Majid Yavarian, Mohammad Hossein Sanati, Somayeh Torfi

Journal:

Frontiers in Biology

Year:

2011

Language:

english

File:

PDF, 238 KB

english, 2011

5

Four novel mutations of the BCKDHA, BCKDHB and DBT genes in Iranian patients with maple syrup urine disease

Zeynalzadeh, Monica, Tafazoli, Alireza, Aarabi, Azadeh, Moghaddassian, Morteza, Ashrafzadeh, Farah, Houshmand, Massoud, Taghehchian, Negin, Abbaszadegan, Mohammad Reza

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2018

Language:

english

File:

PDF, 3.64 MB

english, 2018

6

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia

Massoud Houshmand, Mehdi Shafa Shariat Panahi, Shahriar Nafisi, Akbar Soltanzadeh, Fawziah M. Alkandari

Journal:

Year:

2006

Language:

english

File:

PDF, 188 KB

english, 2006

7

2142 CODING REGION ANALYSIS OF VITAMIN D RECEPTOR GENE AND ITS ASSOCIATION WITH ACTIVE CALCIUM STONE DISEASE

Basiri, Abbas, Shakhssalim, Nasser, Houshmand, Massoud, Kashi, Amir, Pakmanesh, Hamid

Journal:

The Journal of Urology

Year:

2011

Language:

english

File:

PDF, 45 KB

english, 2011

8

India's monsoons more variable than thought

Basiri, Abbas, Shakhssalim, Nasser, Houshmand, Massoud, Kashi, Amir, Pakmanesh, Hamid

Journal:

Year:

2007

Language:

english

File:

PDF, 137 KB

english, 2007

9

Different on the abundance of Pampus argenteus in Persian Gulf exceeding in variety comparing to Gulf of Oman

Sheibaninia, Atena, Nejatkhah Manavi, Parisa, Houshmand, Massoud

Journal:

Mitochondrial DNA Part B

Year:

2017

Language:

english

File:

PDF, 796 KB

english, 2017

10

De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring

Már H. Tulinius, Massoud Houshmand, Nils-Göran Larsson, Elisabeth Holme, Anders Oldfors, Eva Holmberg, Jan Wahlström

Journal:

Year:

1995

Language:

english

File:

PDF, 434 KB

english, 1995

11

[Corrigendum] Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C

Masserrat, Abbas, Sharifpanah, Fatemeh, Akbari, Leila, Tonekaboni, Seyed, Karimzadeh, Parvaneh, Asharafi, Mahmood, Mazrouei, Safoura, Sauer, Heinrich, Houshmand, Massoud

Journal:

Biomedical Reports

Year:

2018

File:

PDF, 178 KB

2018

12

Four Novel p.N385K, p.V36A, c.1033–1034insT and c.1417–1418delCT Mutations in the Sphingomyelin Phosphodiesterase 1 (SMPD1) Gene in Patients with Types A and B Niemann-Pick Disease (NPD)

Manshadi, Masoumeh, Kamalidehghan, Behnam, Keshavarzi, Fatemeh, Aryani, Omid, Dadgar, Sepideh, Arastehkani, Ahoora, Tondar, Mahdi, Ahmadipour, Fatemeh, Meng, Goh, Houshmand, Massoud

Journal:

International Journal of Molecular Sciences

Year:

2015

Language:

english

File:

PDF, 484 KB

english, 2015

13

The mitochondrialATPase6gene is more susceptible to mutation than theATPase8gene in breast cancer patients

Ghaffarpour, Massoud, Mahdian, Reza, Fereidooni, Forouzandeh, Kamalidehghan, Behnam, Moazami, Nasrin, Houshmand, Massoud

Journal:

Cancer Cell International

Year:

2014

Language:

english

File:

PDF, 207 KB

english, 2014

14

Genetic Polymorphisms in Calcitonin Receptor Gene and Risk for Recurrent Kidney Calcium Stone Disease

Shakhssalim, Nasser, Basiri, Abbas, Houshmand, Massoud, Pakmanesh, Hamid, Golestan, Banafsheh, Azadvari, Mohaddeseh, Aryan, Hajar, Kashi, Amir H.

Journal:

Urologia Internationalis

Year:

2014

Language:

english

File:

PDF, 402 KB

english, 2014

15

Allele Frequency Distribution Data for D8S1132, D8S1779, D8S514, and D8S1743 in Four Ethnic Groups in Relation to Metabolic Syndrome: Tehran Lipid and Glucose Study

Maryam Sadat Daneshpour, Suad Alfadhli, Massoud Houshmand, Sirous Zeinali, Mehdi Hedayati, Maryam Zarkesh, Amir Abbas Momenan, Fereidoun Azizi

Journal:

Biochemical Genetics

Year:

2009

Language:

english

File:

PDF, 190 KB

english, 2009

16

Use of D11S2179 and D11S1343 as Markers for Prenatal Diagnosis of Ataxia Telangiectasia in Iranian Patients

Behnaz Bayat, Massoud Houshmand, Mohammad Hossein Sanati, Mostafa Moin, Mehdi Shafa Shariat Panahi, Seyed Ahmad Aleyasin, Anna Isaian, Abolhasan Farhoodi

Journal:

Archives of Medical Research

Year:

2007

Language:

english

File:

PDF, 111 KB

english, 2007

17

Complex I deficiency in Persian multiple sclerosis patients

Hassan H. Kumleh, Gholam H. Riazi, Massoud Houshmand, Mohammad H. Sanati, Kourosh Gharagozli, Mehdi Shafa

Journal:

Journal of the Neurological Sciences

Year:

2006

Language:

english

File:

PDF, 109 KB

english, 2006

18

Establishment and characterization of two human breast carcinoma cell lines by spontaneous immortalization: Discordance between Estrogen, Progesterone and HER2/neu receptors of breast carcinoma tissues with derived cell lines

Behnam Kamalidehghan, Massoud Houshmand, Fereydoun Kamalidehghan, Narges Jafarzadeh, Shahram Azari, Sharifah Noor Akmal, Rozita Rosli

Journal:

Cancer Cell International

Year:

2012

Language:

english

File:

PDF, 2.46 MB

english, 2012

19

Investigation on Mitochondrial tRNALeu/Lys, NDI and ATPase 6/8 in Iranian Multiple Sclerosis Patients

Solmaz Etemad Ahari, Massoud Houshmand, Mehdi Shafa Shariat Panahi, Sadaf Kasraie, Mostafa Moin, Mohammad Ali Bahar

Journal:

Cellular and Molecular Neurobiology

Year:

2007

Language:

english

File:

PDF, 133 KB

english, 2007

20

A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia

Mohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, Shahriar Nafissi, Barbara Scheiber-Mojdehkar, Mehri Khatami

Journal:

Cellular and Molecular Neurobiology

Year:

2009

Language:

english

File:

PDF, 265 KB

english, 2009

21

Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)

Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Aryani, Omid, Sadeghizadeh, Majid, Mossalaeie, Mir Majid

Journal:

Molecular Biology Reports

Year:

2013

Language:

english

File:

PDF, 188 KB

english, 2013

22

New Pathogenic Variations of Mitochondrial DNA in Alzheimer Disease

Sheibani-Nia, Samira, Azadfar, Parisa, Akbari, Leila, Assarzadegan, Farhad, Kamalıdehghan, Behnam, Maroof, Hamid R., Houshmand, Massoud

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 47 KB

english, 2014

23

Prevalence of the CYP2C192 (681 G>A), 3 (636 G>A) and *17 (‑806 C>T) alleles among an Iranian population of different ethnicities

Dehbozorgi, Mahshid, Kamalidehghan, Behnam, Hosseini, Iman, Dehghanfard, Zahra, Sangtarash, Mohammad, Firoozi, Maryam, Ahmadipour, Fatemeh, Meng, Goh, Houshmand, Massoud

Journal:

Molecular Medicine Reports

Year:

2018

Language:

english

File:

PDF, 1.24 MB

english, 2018

24

Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment

Falah, Masoumeh, Najafi, Mohammad, Houshmand, Massoud, Farhadi, Mohammad

Journal:

Clinical Interventions in Aging

Year:

2016

Language:

english

File:

PDF, 582 KB

english, 2016

25

Comprehensive study of mtDNA among Southwest Asian dogs contradicts independent domestication of wolf, but implies dog–wolf hybridization

Arman Ardalan, Cornelya F. C. Kluetsch, Ai-bing Zhang, Metin Erdogan, Mathias Uhlén, Massoud Houshmand, Cafer Tepeli, Seyed Reza Miraei Ashtiani, Peter Savolainen

Journal:

Ecology and Evolution

Year:

2011

Language:

english

File:

PDF, 688 KB

english, 2011

26

Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber’s hereditary optic neuropathy (LHON)

Rezvani, Zahra, Didari, Elmira, Arastehkani, Ahoura, Ghodsinejad, Vadieh, Aryani, Omid, Kamalidehghan, Behnam, Houshmand, Massoud

Journal:

Molecular Biology Reports

Year:

2013

Language:

english

File:

PDF, 192 KB

english, 2013

27

Mitochondrial tRNALeu/Lys and ATPase 6/8 Gene Variations in Spinocerebellar Ataxias

Safaei, Sepideh, Houshmand, Massoud, Banoei, Mohammad Mehdi, Panahi, Mehdi Shafa Shariat, Nafisi, Shahriar, Parivar, Kazem, Rostami, Maryam, Shariati, Parvin

Journal:

Neurodegenerative Diseases

Year:

2009

Language:

english

File:

PDF, 138 KB

english, 2009

28

Early-Onset Alzheimer's Disease in Two Iranian Families: A Genetic Study

Noroozian, Maryam, Azadfar, Parisa, Akbari, Leila, Sadeghi, Arghavan, Houshmand, Massoud, Vousooghi, Nasim, Zarrindast, Mohammad Reza, Minagar, Alireza

Journal:

Dementia and Geriatric Cognitive Disorders

Year:

2014

Language:

english

File:

PDF, 482 KB

english, 2014

29

The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer

Nasser Shakhssalim,Massoud Houshmand,Behnam Kamalidehghan…

Journal:

Cancer Cell International

Year:

2013

Language:

english

File:

PDF, 1.11 MB

english, 2013

30

Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration

Rezaee, Ali Reza, Banoei, Mohammad Mehdi, Khalili, Elham, Houshmand, Massoud

Journal:

The Scientific World JOURNAL

Year:

2012

Language:

english

File:

PDF, 1.31 MB

english, 2012

31

Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: A case study

Dowlati, Mohammad Ali, Derakhshandeh-peykar, Pupak, Houshmand, Massoud, Farhadi, Mohammad, Shojaei, Azadeh, Bazzaz, Javad Tavakkoly

Journal:

Mitochondrial DNA

Year:

2013

Language:

english

File:

PDF, 119 KB

english, 2013

32

Coding region analysis of vitamin D receptor gene and its association with active calcium stone disease

Abbas Basiri, Nasser Shakhssalim, Massoud Houshmand, Amir H. Kashi, Mohaddeseh Azadvari, Banafsheh Golestan, Esmaeel Mohammadi Pargoo, Hamid Pakmanesh

Journal:

Year:

2012

Language:

english

File:

PDF, 204 KB

english, 2012

33

Variation of DAT1 VNTR Alleles and Genotypes Among Old Ethnic Groups in Mesopotamia to the Oxus Region

Banoei, Mohammad Mehdi, Chaleshtori, Morteza Hashemzadeh, Sanati, Mohammad Hossein, Shariati, Parvin, Houshmand, Massoud, Majidizadeh, Tayebeh, Soltani, Niloofar Jahangir, Golalipour, Massoud

Journal:

Year:

2008

Language:

english

File:

PDF, 127 KB

english, 2008

34

A novel PANK2 gene mutation in a Persian boy: The first report from Iran

Aryani, Omid, Houshmand, Massoud, Fatehi, Farzad

Journal:

Clinical Neurology and Neurosurgery

Year:

2013

Language:

english

File:

PDF, 490 KB

english, 2013

35

Cutis Laxa Type II with Mutation in the Pyrroline-5-Carboxylate Reductase 1 Gene

Nouri, Nayereh, Aryani, Omid, Nouri, Narges, Kamalidehghan, Behnam, Houshmand, Massoud

Journal:

Pediatric Dermatology

Year:

2013

Language:

english

File:

PDF, 115 KB

english, 2013

36

Vitamin D receptor homozygote mutant tt and bb are associated with susceptibility to pulmonary tuberculosis in the Iranian population

Mohammad Mehdi Banoei, Mehdi Seyed Mirsaeidi, Massoud Houshmand, Payam Tabarsi, Golnaz Ebrahimi, Laleh Zargari, Baharak Houshiar Kashani, Mohammad Reza Masjedi, Seyed Davood Mansouri, Julio Ramirez

Journal:

International Journal of Infectious Diseases

Year:

2010

Language:

english

File:

PDF, 88 KB

english, 2010

37

PARIS.

Aryani, Omid, Houshmand, Massoud, Fatehi, Farzad

Journal:

Year:

1908

Language:

english

File:

PDF, 415 KB

english, 1908

38

Pitfalls for Common Mitochondrial DNA Deletion (ΔmtDNA4977) As a Biomarker of Cancer

Kamalidehghan, Behnam, Houshmand, Massoud

Journal:

Archives of Medical Research

Year:

2013

Language:

english

File:

PDF, 62 KB

english, 2013

39

Phylogenetic analysis of yellow-bar angelfish (Pomacanthus maculosus) of the Persian Gulf using cytochrome b sequences

Samiei Zafarghandi, Samira, Nejatkhah Manavi, Parisa, Houshmand, Seyed Massoud

Journal:

Marine Biodiversity Records

Year:

2013

Language:

english

File:

PDF, 304 KB

english, 2013

40

Mitochondrial G8292A and C8794T mutations in patients with Niemann‑Pick disease type C

Masserrat, Abbas, Sharifpanah, Fatemeh, Akbari, Leila, Tonekaboni, Seyed, Karimzadeh, Parvaneh, Asharafi, Mahmood Reza, Mazouei, Safoura, Sauer, Heinrich, Houshmand, Massoud

Journal:

Biomedical Reports

Year:

2018

File:

PDF, 479 KB

2018

41

Prevalence of the CYP2D610 (C100T), 4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicities

Kamalidehghan, Behnam, Vejdandoust, Faramarz, Bagheri, Ali, Houshmand, Massoud, Azadfar, Parisa, Akbari, Leila, Haghshenas Moghadam, Maryam, Hossein Sangtarash, Mohammad, Ahmadipour, Fatemeh, Yong Men

Journal:

Drug Design Development and Therapy

Year:

2015

Language:

english

File:

PDF, 2.83 MB

english, 2015

42

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

Kamalidehghan, Behnam, Balali, Maryam, Houshmand, Massoud, Farhadi, Mohammad, Dehghani Ashkzari, Mahmoud, Rezaei Hemami, Mohsen, Arabzadeh, Hossein, Falah, Masoumeh, Yong Meng, Goh, Ahmadipour, Fateme

Journal:

Therapeutics and Clinical Risk Management

Year:

2016

Language:

english

File:

PDF, 2.63 MB

english, 2016

43

Mitochondrial D-Loop Variation in Leber Hereditary Neuropathy Patients Harboring Primary G11778A, G3460A, T14484C Mutations: J and W Haplogroups as High-Risk Factors

Mehdi Shafa Shariat Panahi, Massoud Houshmand, Abdol Reza Tabassi

Journal:

Archives of Medical Research

Year:

2006

Language:

english

File:

PDF, 113 KB

english, 2006

44

RAD51 polymorphisms and breast cancer risk

Mojgan Hosseini, Massoud Houshmand, Ahmad Ebrahimi

Journal:

Molecular Biology Reports

Year:

2013

Language:

english

File:

PDF, 230 KB

english, 2013

45

Клинический полиморфизм и подходы к лечению нарушений ритма сердца в семье с делецией akpq1505-1507 в гене scn5a

Сабер Сиамак,Houshmand Massoud,Eftekharzadeh Mahmoud

Journal:

Вестник Российской академии медицинских наук

Year:

2014

File:

PDF, 367 KB

2014

46

ΔmtDNA4977 Is More Common in Non-tumoral Cells from Gastric Cancer Sample

Behnam Kamalidehghan, Massoud Houshmand, Patimah Ismail, Mehdi Shafa Shariat Panahi, Mohammad Hassan Hosseini Akbari

Journal:

Archives of Medical Research

Year:

2006

Language:

english

File:

PDF, 152 KB

english, 2006

47

Downregulation of miR-34a in breast tumors is not associated with either p53 mutations or promoter hypermethylation while it correlates with metastasis

Arash Javeri, Massoud Ghaffarpour, Masoumeh Fakhr Taha, Massoud Houshmand

Journal:

Medical Oncology

Year:

2013

Language:

english

File:

PDF, 421 KB

english, 2013

48

Investigation of Psen1&2 Genes in Early Onset Alzheimer’s Disease Patients

Akbari, Leila, Azadfar, Parisa, Sheibani-Nia, Samira, Noroozıan, Maryam, Assarzadegan, Farhad, Houshmand, Massoud

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 56 KB

english, 2014

49

Complex I and ATP Content Deficiency in Lymphocytes from Friedreich's Ataxia

Heidari, Mohammad Mehdi, Houshmand, Massoud, Hosseinkhani, Saman, Nafissi, Shahriar, Khatami, Mehri

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2009

File:

PDF, 187 KB

2009

50

Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran

Nourizadeh, Maryam, Shakerian, Leila, Borte, Stephan, Fazlollahi, Mohammadreza, Badalzadeh, Mohsen, Houshmand, Massoud, Alizadeh, Zahra, Dalili, Hossein, Rashidi-Nezhad, Ali, Kazemnejad, Anoshirvan, M

Journal:

Scandinavian Journal of Immunology

Year:

2018

Language:

english

File:

PDF, 573 KB

english, 2018

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