Your search returned 26 results.

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	1.	Increased levels of mitochondrial DNA copy number in patients with vitiligo. [electronic resource] by Vaseghi, H Houshmand, M Jadali, Z Producer: 20180404 In: Clinical and experimental dermatology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Leber hereditary optic neuropathy: do folate pathway gene alterations influence the expression of mitochondrial DNA mutation? [electronic resource] by Aleyasin, A Ghazanfari, M Houshmand, M Producer: 20130704 In: Iranian journal of public health vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel Mutations in Sandhoff Disease: A Molecular Analysis among Iranian Cohort of Infantile Patients. [electronic resource] by Aryan, H Aryani, O Banihashemi, K Zaman, T Houshmand, M Producer: 20121101 In: Iranian journal of public health vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	4.	Effect of aerobic exercise training on mtDNA deletion in soleus muscle of trained and untrained Wistar rats. [electronic resource] by Jafari, A Hosseinpourfaizi, M A Houshmand, M Ravasi, A A Producer: 20050815 In: British journal of sports medicine vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations. [electronic resource] by Jalalirad, M Houshmand, M Mirfakhraie, R Goharbari, M H Mirzajani, F Producer: 20050211 In: Journal of tropical pediatrics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne. [electronic resource] by Houshmand, M Larsson, N G Oldfors, A Tulinius, M Holme, E Producer: 19960920 In: Human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspring. [electronic resource] by Houshmand, M Lindberg, C Moslemi, A R Oldfors, A Holme, E Producer: 19990713 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection? [electronic resource] by Houshmand, M Holme, E Hanson, C Wennerholm, U B Hamberger, L Producer: 19970718 In: Journal of assisted reproduction and genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Effects of prebiotic, protein level, and stocking density on performance, immunity, and stress indicators of broilers. [electronic resource] by Houshmand, M Azhar, K Zulkifli, I Bejo, M H Kamyab, A Producer: 20120329 In: Poultry science vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran. [electronic resource] by Houshmand, M Sanati, M-H Rashedi, I Sharifpanah, F Asghari, E Lotfi, J Producer: 20040506 In: European neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Plasma glucose lowering effect of the wild Satureja khuzestanica Jamzad essential oil in diabetic rats: role of decreased gluconeogenesis. [electronic resource] by Shahsavari, R Ehsani-Zonouz, A Houshmand, M Salehnia, A Ahangari, G Firoozrai, M Producer: 20090723 In: Pakistan journal of biological sciences : PJBS vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	The first study of galactose-1-phosphate uridyl transferase mutations in Iranian galactosemia patients. [electronic resource] by Mirzajani, F Mirfakhraie, R Nabati, F Tabatabaei, N Naghibzadeh Talachian, E Houshmand, M Producer: 20060829 In: Clinical biochemistry vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Effects of non-antibiotic feed additives on performance, tibial dyschondroplasia incidence and tibia characteristics of broilers fed low-calcium diets. [electronic resource] by Houshmand, M Azhar, K Zulkifli, I Bejo, M H Meimandipour, A Kamyab, A Producer: 20110816 In: Journal of animal physiology and animal nutrition vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene. [electronic resource] by Houshmand, M Mahmoudi, T Panahi, M Shafa Shariat Seyedena, Y Saber, S Ataei, M Producer: 20070409 In: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. [electronic resource] by Houshmand, M Larsson, N G Holme, E Oldfors, A Tulinius, M H Andersen, O Producer: 19940513 In: Biochimica et biophysica acta vol. 1226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Application of multiplex PCR with histopathologic features for detection of familial breast cancer in formalin-fixed, paraffin-embedded histologic specimens. [electronic resource] by Rassi, H Houshmand, M Hashemi, M Majidzadeh, K Akbari, M H Hosseini Panahi, M Shafa Shariat Producer: 20080808 In: TSitologiia i genetika vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	17.	De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring. [electronic resource] by Tulinius, M H Houshmand, M Larsson, N G Holme, E Oldfors, A Holmberg, E Wahlström, J Producer: 19950928 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients. [electronic resource] by Houshmand, M Sharifpanah, F Tabasi, A Sanati, M-H Vakilian, M Lavasani, S H Joughehdoust, S Producer: 20040617 In: Annals of the New York Academy of Sciences vol. 1011 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions. [electronic resource] by Tulinius, M H Oldfors, A Holme, E Larsson, N G Houshmand, M Fahleson, P Sigström, L Kristiansson, B Producer: 19950427 In: European journal of pediatrics vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients. [electronic resource] by Houshmand, M Sanati, M H Babrzadeh, F Ardalan, A Teimori, M Vakilian, M Akuchekian, M Farhud, D Lotfi, J Producer: 20060203 In: Multiple sclerosis (Houndmills, Basingstoke, England) vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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