Search Results - "PANAHI, Mehdi Shafa Shariat"

Mitochondrial DNA sequence diversity in three ethnic populations from the South-west Iran: a preliminary study by Davoudi-Dehaghani, Elham, Foroughmand, Ali Mohammad, Saffari, Babak, Houshmand, Massoud, Galehdari, Hamid, Shafa Shariat Panahi, Mehdi, Yavarian, Majid, Sanati, Mohammad Hossein, Torfi, Somayeh

“…To investigate the genetic structure of human populations in the South-west region of Iran, mitochondrial first hypervariable DNA sequences were obtained from…”
Get full text

Do haplogroups H and U act to increase the penetrance of Alzheimer's disease? by Fesahat, Farzaneh, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Gharagozli, Kurosh, Mirzajani, Farzaneh

“…1. Alzheimer's disease (AD) is the most common form of dementia in the elderly in which interplay between genes and the environment is supposed to be involved…”
Get full text

Mitochondrial D-Loop Variation in Leber Hereditary Neuropathy Patients Harboring Primary G11778A, G3460A, T14484C Mutations: J and W Haplogroups as High-Risk Factors by Shafa Shariat Panahi, Mehdi, Houshmand, Massoud, Tabassi, Abdol Reza

“…Leber hereditary optic neuropathy (LHON) is a maternally inherited form of retinal ganglion cell degeneration leading to optic atrophy in young adults. It is…”
Get full text

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia by Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Nafisi, Shahriar, Soltanzadeh, Akbar, Alkandari, Fawziah M

“…Friedreich's Ataxia (FA) is the commonest genetic cause of ataxia and is associated with the expansion of a GAA repeat in intron 1 of the frataxin gene. Iron…”
Get full text

Use of D11S2179 and D11S1343 as Markers for Prenatal Diagnosis of Ataxia Telangiectasia in Iranian Patients by Bayat, Behnaz, Houshmand, Massoud, Sanati, Mohammad Hossein, Moin, Mostafa, Shariat Panahi, Mehdi Shafa, Aleyasin, Seyed Ahmad, Isaian, Anna, Farhoodi, Abolhasan

“…Ataxia telangiectasia (AT) is an autosomal recessive disorder with an estimated prevalence of 1/40,000 to 1/100,000 in reported populations. There is a 25%…”
Get full text

Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion? by Banoei, Mohammad Mehdi, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Shariati, Parvin, Rostami, Maryam, Manshadi, Masoumeh Dehghan, Majidizadeh, Tayebeh

“…The mitochondrial DNA (mtDNA) may play an essential role in the pathogenesis of the respiratory chain complex activities in neurodegenerative disorders such as…”
Get full text

Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients by Ahari, Solmaz Etemad, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Kasraie, Sadaf, Moin, Mostafa, Bahar, Mohammad Ali

“…As with chromosomal DNA, the mitochondrial DNA (mtDNA) can contain mutations that are highly pathogenic . In fact, many diseases of the central nervous system…”
Get full text

Investigation of tRNALeu/Lys and ATPase 6 Genes Mutations in Huntington’s Disease by Kasraie, Sadaf, Houshmand, Massoud, Banoei, Mohammad Mehdi, Ahari, Solmaz Etemad, Panahi, Mehdi Shafa Shariat, Shariati, Parvin, Bahar, Mohammad, Moin, Mostafa

“…Huntington disease (HD) is a genetically dominant condition caused by expanded CAG repeats which code for glutamine in the HD gene product, huntingtin…”
Get full text

Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's disease by Kasraie, Sadaf, Houshmand, Massoud, Banoei, Mohammad Mehdi, Ahari, Solmaz Etemad, Panahi, Mehdi Shafa Shariat, Shariati, Parvin, Bahar, Mohammad, Moin, Mostafa

“…Huntington disease (HD) is a genetically dominant condition caused by expanded CAG repeats which code for glutamine in the HD gene product, huntingtin…”
Get full text

Tumoral Cell mtDNA ∼8.9 kb Deletion Is More Common than Other Deletions in Gastric Cancer by Kamalidehghan, Behnam, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Abbaszadegan, Mohammad Reza, Ismail, Patimah, Shiroudi, Mahnaz Bagher

“…The aim of the study was to clarify the role of deletion of mitochondrial DNA (mtDNA) in gastric carcinogenesis and to determine prevalence of mitochondrial…”
Get full text

Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias by Safaei, Sepideh, Houshmand, Massoud, Banoei, Mohammad Mehdi, Panahi, Mehdi Shafa Shariat, Nafisi, Shahriar, Parivar, Kazem, Rostami, Maryam, Shariati, Parvin

“…The spinocerebellar ataxias (SCA) comprise a heterogeneous group of severe late-onset neurodegenerative diseases that are promoted by the expansion of a…”
Get more information

Investigation on Mitochondrial tRNALeu/Lys, NDI and ATPase 6/8 in Iranian Multiple Sclerosis Patients by Ahari, Solmaz Etemad, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Kasraie, Sadaf, Moin, Mostafa, Bahar, Mohammad Ali

Get full text

Investigation on Mitochondrial tRNA super(Leu/Lys), NDI and ATPase 6/8 in Iranian Multiple Sclerosis Patients by Ahari, Solmaz Etemad, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Kasraie, Sadaf, Moin, Mostafa, Bahar, Mohammad Ali

“…As with chromosomal DNA, the mitochondrial DNA (mtDNA) can contain mutations that are highly pathogenic .In fact, many diseases of the central nervous system…”
Get full text

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor by Hassani-Kumleh, Hassan, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Riazi, Gholam Hossein, Sanati, Mohammad Hossein, Gharagozli, Kurosh, Ghabaee, Mojdeh

“…: Multiple Sclerosis (MS) is a multifocal demyelinating central nervous system disorder in which interplay between genes and the environment are supposed to be…”
Get full text

Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancer by Kamalidehghan, Behnam, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Abbaszadegan, Mohammad Reza, Ismail, Patimah, Shiroudi, Mahnaz Bagher

“…The aim of the study was to clarify the role of deletion of mitochondrial DNA (mtDNA) in gastric carcinogenesis and to determine prevalence of mitochondrial…”
Get full text

Delta mtDNA4977 is more common in non-tumoral cells from gastric cancer sample by Kamalidehghan, Behnam, Houshmand, Massoud, Ismail, Patimah, Panahi, Mehdi Shafa Shariat, Akbari, Mohammad Hassan Hosseini

“…The aim of this study was to determine the frequency of delta mtDNA4977 in tumoral cells as compared with adjacent normal cells in gastric cancer. In order to…”
Get full text

ΔmtDNA 4977 Is More Common in Non-tumoral Cells from Gastric Cancer Sample by Kamalidehghan, Behnam, Houshmand, Massoud, Ismail, Patimah, Panahi, Mehdi Shafa Shariat, Akbari, Mohammad Hassan Hosseini

“…The aim of this study was to determine the frequency of ΔmtDNA 4977 in tumoral cells as compared with adjacent normal cells in gastric cancer. In order to…”
Get full text

Do mitochondrial DNA haplogroups play a role in susceptibility to tuberculosis? by HOUSHMAND, Massoud, BANOEI, Mohammad Mehdi, TABARSI, Payam, PANAHI, Mehdi Shafa Shariat, KASHANI, Baharak Hooshiar, EBRAHIMI, Golnaz, ZARGAR, Laleh, FARNIA, Parissa, MORRIS, Matthew W., MANSOURI, Davood, VELAYATI, Ali Akbar, MIRSAEIDI, Mehdi S.

“…Background and objectives:  Mitochondrial DNA has a unique role in ATP production and subsequent mitochondrial reactive oxygen species (ROS) production in…”
Get full text