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Theses and Dissertations
0
0
Developing Gene Therapy for Duchenne muscular dystrophy using Adeno Associated virus (AAV) Expressing Estrogen Related Receptor Gamma (ERRγ)
ALSiyabi, Muzna
Muzna ALSiyabi
2018
Developing Gene Therapy for Duchenne muscular dystrophy using Adeno Associated virus (AAV) Expressing Estrogen Related Receptor Gamma (ERRγ)
Journal articles
0
0
Cleidocranial dysplasia : a rare cause of disproportionate severe short stature.
Bhat, Manzoor.
Oman Medical Specialty Board.
2012-09
Cleidocranial dysplasia : a rare cause of disproportionate severe short stature.
Journal articles
2
0
Implications of a Chr7q21.11 microdeletion and the role of the PCLO gene in developmental delay.
Mazzaschi, Roberto L.
College of Medicine, Sultan Qaboos University.
2013-05
Implications of a Chr7q21.11 microdeletion and the role of the PCLO gene in developmental delay.
Journal articles
0
0
Detection of CTX-M-15 among uropathogenic escherichia coli isolated from five major hospitals in Tripoli, Libya.
Zorgani, Abdulaziz.
Oman Medical Specialty Board.
2017-07
Detection of CTX-M-15 among uropathogenic escherichia coli isolated from five major hospitals in Tripoli, Libya.
Journal articles
0
0
Genetic biomarkers in association with depressive disorder in UAE residents : a pilot case study.
Mahmood, Nailah.
Oman Medical Specialty Board.
2021-07
Genetic biomarkers in association with depressive disorder in UAE residents : a pilot case study.
Journal articles
0
0
Characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplication in the FLT3 gene.
Al-Mawaliyah, Adhra.
Oman Medical Specialty Board.
2013-11
Characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplication in the FLT3 gene.
Theses and Dissertations
0
0
Apolipoprotein E gene polymorphism with ischemic stroke in Omani patients : a hospital-based case-control study
Gharbal, Ali Husain.
Sultan Qaboos University
2016
Apolipoprotein E gene polymorphism with ischemic stroke in Omani patients : a hospital-based case-control study
Journal articles
0
0
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
Scott, Patrick.
Oman Medical Specialty Board.
2016-05
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
Theses and Dissertations
1
0
Agrobacterium Mediated Transformation of cry1C Gene into Omani Tobacco Cultivar
Al-Maamariyah, Alghalyia Humaid Khamis.
Sultan Qaboos University
2007
Agrobacterium Mediated Transformation of cry1C Gene into Omani Tobacco Cultivar
Journal articles
0
0
The expression of activating receptor gene of natural killer cells (KLRC3) in patients with Type 1 diabetes mellitus (T1DM).
Shalaby, Dalia.
Oman Medical Specialty Board.
2017-07
The expression of activating receptor gene of natural killer cells (KLRC3) in patients with Type 1 diabetes mellitus (T1DM).
Journal articles
0
0
Evaluation of the role of -137G/C single nucleotide polymorphism (rs187238) and gene expression levels of the IL-18 in patients with coronary artery disease.
Hoseini, Fatemeh.
Oman Medical Specialty Board.
2018-03
Evaluation of the role of -137G/C single nucleotide polymorphism (rs187238) and gene expression levels of the IL-18 in patients with coronary artery disease.
Journal articles
0
0
A novel mutation causing 17-β-hydroxysteroid dehydrogenase Type 3 deficiency in an Omani child : first case report and review of literature.
Al-Sinaniyah, Aisha.
Oman Medical Specialty Board.
2015-03
A novel mutation causing 17-β-hydroxysteroid dehydrogenase Type 3 deficiency in an Omani child : first case report and review of literature.
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Journal articles
(9)
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Journal articles
(9)
Theses and Dissertations
(3)
Subject
Gene expression
(4)
17--hydroxysteriod dehydrogenase Type 3 deficiency
(1)
Acute myeloid leukemia
(1)
Agrobacterium
(1)
Ambiguous genitalia
(1)
Apolipoprotein E gene.
(1)
Apolipoproteins
(1)
Biomarkers
(1)
Brain Ischemia
(1)
Cerebrovascular disease
(1)
Charcot-Marie-tooth disease, Type 4B1
(1)
Cleidocranial dysplasia
(1)
Coronary artery disease
(1)
CTX-M-15 gene
(1)
Delta 4-androstenedione
(1)
Depressive disorder
(1)
Developmental disabilities--Diagnosis
(1)
Diabetes mellitus, Type 1
(1)
Disorder of sex development, 46,XY
(1)
E. coli
(1)
ESBL
(1)
Estrone
(1)
FLT3 gene
(1)
HSD17B3 gene
(1)
Interleukin-18
(1)
Killer cells, Natural
(1)
KLRC3 protein, Human
(1)
Libya
(1)
M1
(1)
MTMR2 gene
(1)
Mutation
(1)
Optic neuritis
(1)
Plant gene isolation
(1)
Plant genetic transformation
(1)
Polymerase chain reaction
(1)
Polymorphism, Restriction fragment length
(1)
Prognosis
(1)
Schwannoma
(1)
Short stature
(1)
Skeletal dysplasia
(1)
Skeletal muscle^ gene therapy^ AAV virus^ ERRγ
(1)
SLC6A4 protein, Human
(1)
Stroke
(1)
Tandem duplication
(1)
Testosterone
(1)
tobacco
(1)
Transgenic plants
(1)
Author
Al-Maamariyah, Alghalyia Humaid Khamis.
(1)
Al-Mawaliyah, Adhra.
(1)
Al-Sinaniyah, Aisha.
(1)
ALSiyabi, Muzna
(1)
Bhat, Manzoor.
(1)
Gharbal, Ali Husain.
(1)
Hoseini, Fatemeh.
(1)
Mahmood, Nailah.
(1)
Mazzaschi, Roberto L.
(1)
Scott, Patrick.
(1)
Shalaby, Dalia.
(1)
Zorgani, Abdulaziz.
(1)
Publisher
Oman Medical Specialty Board
(8)
Sultan Qaboos University
(2)
College of Medicine Sultan Qaboos University
(1)
Muzna ALSiyabi
(1)
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