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مقالات

Genetic diversity for three populations of Rainbow Trout (Oncorhynchus mykiss)‎ based on sequencing of mtDNA genes

By: Abd Allah, Taqi; Nassiri, Muhammad Rida; Safari, Umid…[et al.]. Marsh Bulletin. Vol. 14, no. 1 (Apr. 2019), pp.1-10, 10 p.

Subjects: Biological diversity; Fisheries; Mutation; Nucleic acids; Rainbow trout

أوراق مؤتمرات

Detection for MECA gene in Egyptian clinical Staphylococcus aureus samples and study their genotoxic activity

By: Hasan, Marwah; Ibrahim, Samir Abd al-Aziz; Abd al-Raziq, Ashraf Bakri…[et al.]. . Arab Universities Journal of Agricultural Sciences. Vol. 27, no. 1 (s) (2019), pp.529-537, 9 p.

Subjects: Activities; Bone marrow; Damages; Mutation; Tests

أوراق مؤتمرات

Development of in vitro somaclonal variation for Pelargonium Graveolens L'herit, Ait

By: Haridi, Rasha Ibrahim Muhammad; Rashid, Muhammad Abd al-Salam; Sidqi, Mahasin Muhammad Abd al-Ghani. Arab Universities Journal of Agricultural Sciences. Vol. 27, no. 1 (s) (2019), pp.563-577, 15 p.

Subjects: Mutation

مقالات

Anticancer effects of tow traditional drinks hibiscus (Hibiscus sabdariffa linn)‎ and liquorice (Glycyrrhiza glabra)‎

By: al-Sayyid, Abd al-Alim Ismail Ibrahim; Jumah, Ayman Muhammad; Abd al-Munim, Jamal Muhammad…[et al.]. Zagazig Journal for Agricultural Researches. Vol. 46, no. 1 (2019), pp.115-122, 8 p.

Subjects: Breast; Cancer; Cancer cell; Damages; Mutation

مقالات

Detection of mutagenicity in some cured meat products using Ames Test

By: Hasan, Kariman Muhammad; Mahmud, Ramadan Muhammad; Khallaf, Muhammad Faraj…[et al.]. Arab Universities Journal of Agricultural Sciences. Vol. 26, no. 2 D (2018), pp.2411-2417, 7 p.

Subjects: Diagnosis; Food additives; Meat; Molecular aspects; Mutation

رسائل جامعية

Identification of Glucokinase mutations in subjects with gestational diabetes mellitus-Gaza Strip

By: al-Aqqad, Tahir Ahmad Tahir. Master; Islamic University; 2018

Subjects: Diabetes; Gaza Strip; Glucokinase; Mutation; Pregnancy

أوراق مؤتمرات

Genetic variation of ten Iraqi wheat genotypes using (SSR)‎ markers and morphological characterization

By: al-Tamimi, Itaf Jamil Thamir; al-Budayri, Nidal Abd al-Husayn; al-Ghufayli, Milath Kazim Farhud…[et al.]. . International Scientific Conference (3rd : 2018 : Najaf, Iraq) al-Kufa University Journal for Biology. Special issue (2018), pp.34-39, 6 p.

Subjects: Genes; Genetics; Mutation; Wheat

مقالات

Hepatitis B virus precore G1896A mutation in chronic liver disease patients with HBeAg negative serology from North India

By: Kumar, Deepak; Chaudhary, Anis Ahmad; Kar, P.…[et al.]. Saudi Journal of Biological Sciences. Vol. 25, no. 7 (Nov. 2018), pp.1257-1262, 6 p.

Subjects: Hepatitis B; India; Mutation; Patients; Viruses

مقالات

Genetic study of the NOTCH3 gene in CADASIL patients

By: Tarzjani, Sayyidah Parisa Chavoshi; Fadil, Sayyid Abu al-Hasan Shahzadah; Sanati, Muhammad Husayn…[et al.]. The Egyptian Journal of Medical Human Genetics. Vol. 19, no. 4 (Oct. 2018), pp.425-427, 3 p.

Subjects: Cerebral thrombosis; Genes; Mutation; Patients; Receptors (biochemistry)

مقالات

In silico analysis of the functional non-synonymous single nucleotide polymorphisms in the human CYP27B1 gene

By: Rotimi, Solomon O.; Peter, Olamide; Oguntade, Oluwayomi…[et al.]. The Egyptian Journal of Medical Human Genetics. Vol. 19, no. 4 (Oct. 2018), pp.367-378, 12 p.

Subjects: Cancer; Diabetes; Genetic polymorphisms; Mutation; Vitamin D

مقالات

FLT3 receptorCD135 expression by flow cytometry in acute myeloid leukemia : Relation to FLT3 gene mutations and mRNA transcripts

By: Makkawi, Muhammad Amin; Isa, Dina Samir; Hamzah, Muhammad Tarif…[et al.]. The Egyptian Journal of Medical Human Genetics. Vol. 19, no. 4 (Oct. 2018), pp.345-351, 7 p.

Subjects: Acute myeloid leukemia; Mutation; Receptors (biochemistry)

مقالات

Association of c.1298 A>C variation in methylenetetrahydrofolate reductase gene with neural tube defects : case-control study in Syrian population

By: Himaih, Dalal; Abu al-Shamat, Ghaliyah; Nasir al-Din, Hasan. Iraqi Journal of Biotechnology. Vol. 17, no. 2 (Sep. 2018), pp.23-29, 7 p.

Subjects: Methylenetetrahydrofolate reductase; Mutation; Neural tube

مقالات

Molecular detection and analysis of mut l gene from Pseudomonas aeruginosa in urinary tract infection patients

By: Hamzah, Ala Salim. The Iraqi Journal of Agricultural Science. Vol. 49, no. 4 (2018), pp.677-684, 8 p.

Subjects: Inflammation; Mutation; Patients; Pseudomonas aeruginosa; Urinary tract

مقالات

Estimation of genetic variations in different taxa in Brassicaceae by RAPD and ISSR analysis

By: al-Tamimi, Huda Jasim Muhammad. Bulletin of the Iraq Natural History Museum. Vol. 15, no. 1 (2018), pp.1-13, 13 p.

Subjects: Cruciferae; DNA fingerprinting; Genes; Mutation

مقالات

Micropropagation and genetic variations of Cordyline terminalis cv. red top

By: al-Turki, Muhammad Jamal al-Din Muhammad; al-Mahruq, Muhammad al-Sayyid; al-Muqaddim, Huda al-Sayyid…[et al.]. Journal of the Advances in Agricultural Researches. Vol. 23, no. 2 (2018), pp.328-349, 22 p.

Subjects: Cordyline; Mutation

أوراق مؤتمرات

In vitro, induction of salt tolerant potato (Solanum tuberosum l. )‎ plants with gamma irradiation and characterization of genetic variations through sds-page and issr-pcr analysis

By: al-Hitiawi, Dina Y. M.; Rifat, M. H.; Abd al-Sabur, M. S.…[et al.]. . Annals of Agricultural Science, Moshtohor. Vol. 56, Special issue (2018), pp.167-176, 10 p.

Subjects: Gamma ray; Mutation; Potatoes; Salinity

أوراق مؤتمرات

Salmonella lipopolysaccharide-induced thymocyte death and thymic atrophy were related to tlr4-fos jun pathway in chicks (abstract)‎

By: Liu, Huazhen. Annals of Agricultural Science, Moshtohor. Vol. 56, Special issue (2018), pp.35-36, 2 p.

Subjects: Compact disks; DNA; Damages; Mutation; Salmonella typhi

مقالات

Mutational analysis of AGXT gene in Libyan children with primary hyperoxaluria type 1at tripoli children hospital

By: Rhuma, Naziha R.; Fituri, Umar A.; Sabei, Layla T.. Saudi Journal of Kidney Diseases and Transplantation. Vol. 29, no. 1 (Jan. / Feb. 2018), pp.30-38, 9 p.

Subjects: Case studies; Children; Libya; Metabolic disorders; Mutation

مقالات

Effects of static magnetic field on Escherichia coli Mutation

By: Kamil, Fuad Husayn; Qadir, Ishti Muhammad Amin Salim Said. Mesopotamia Journal of Agriculture. Vol. 46, no. 1 (Jan. 2018), pp.265-270, 6 p.

Subjects: Biological control; Escherichia coli; Magnetic fields; Mutation; Physiological effects

مقالات

Genetic variation among selected species of Plectropomus (Family: Serranidae)‎ based on DNA barcoding technique using CO1 nucleotide sequences

By: al-Jahdali, Ramzi Sulayman; Gharabawi, Walid Yusuf. Journal of King Abdul Aziz University : Marine Science. Vol. 27, no. 2 (2017), pp.99-104, 6 p.

Subjects: Fishes; Mutation; Nucleic acids

مقالات

Evaluation of promising mutant lines of canola grown under new reclamation lands (Harsh Lands)‎

By: Amir, I. M.; Sulayman, S. S.; Hasan, A. A.…[et al.]. Arab Journal of Nuclear Sciences and Applications. Vol. 50, no. 3 (Jul. 2017), pp.174-180, 7 p.

Subjects: Agriculture; Canola; Environmental aspects; Gamma ray; Mutation

مقالات

Association of exon 9 FGFR3 mutations and cancer grads in patients with bladder cancer

By: al-Faysal, Abd al-Husayn Muwayt; Bresam, Sabah. Iraqi Journal of Biotechnology. Vol. 15, no. 2 (2016), pp.109-118, 10 p.

Subjects: Bladder; Cancer; Iraq; Mutation; Patients

مقالات

A new missense mutation in PLA2G6 gene among a family with infantile neuroaxonal dystrophy INAD

By: Jibril, Ula; Uebe, Steffen; Reuter, Miriam…[et al.]. Egyptian Pediatric Association Gazette. Vol. 64, no. 4 (Dec. 2016), pp.171-176, 6 p.

Subjects: Brain; Case studies; Children; Diseases; Mutation

مقالات

Distal renal tubular acidosis with nerve deafness secondary to Atp6b1 gene mutation

By: Naveen, Parvathina Sriram; Srikanth, Lokanatha; Venkatesh, Katari…[et al.]. Saudi Journal of Kidney Diseases and Transplantation. Vol. 26, no. 1 (Jan. / Feb. 2015), pp.119-121, 3 p.

Subjects: Deafness; Diseases; Kidneys; Mutation; Patients

مقالات

MRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis

By: Benetti, Elisa; Caridi, Gianluca; Ghiggeri, Gian Marco…[et al.]. Saudi Journal of Kidney Diseases and Transplantation. Vol. 25, no. 4 (2014), pp.854-857, 4 p.

Subjects: Children; Kidneys; Mutation; Proteins; Social structure

مقالات

Does NPHS1 polymorphism modulate P118L mutation in NPHS2?

By: Mir, Sivgi; Bulut, Ipek Kaplan; Sozeri, Betul…[et al.]. Saudi Journal of Kidney Diseases and Transplantation. Vol. 24, no. 6 (2013), pp.1210-1213, 4 p.

Subjects: Children; Diseases; Kidneys; Mutation; Patients

مقالات

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC)‎ : report of three cases with a novel mutation in CLDN19 gene

By: al-Shibli, Ammar; Konrad, Martin; al-Atrash, Ibrahim…[et al.]. Saudi Journal of Kidney Diseases and Transplantation. Vol. 24, no. 2 (2013), pp.338-344, 7 p.

Subjects: Calcium; Case studies; Kidneys; Metabolism; Mutation

مقالات