-
1دورية أكاديمية
المؤلفون: Salam Alkindi, Salma Al-Jadidi, Safa Al-Adawi, Refaat Abdullah Elsadek, Ali Al Madhani, Maryam Al-Nabhani, Anil V. Pathare
المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
مصطلحات موضوعية: Sickle cell disease, Predictors of mortality, Acute chest syndrome, Sepsis, Sudden death, SCD, Medicine, Science
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2045-2322Test
-
2دورية أكاديمية
المؤلفون: Mansour S Al-Moundhri, Maryam Al-Nabhani, Letizia Tarantini, Andrea Baccarelli, Jennifer A Rusiecki
المصدر: PLoS ONE, Vol 5, Iss 12, p e15585 (2010)
وصف الملف: electronic resource
العلاقة: http://europepmc.org/articles/PMC3009731?pdf=renderTest; https://doaj.org/toc/1932-6203Test
-
3
المؤلفون: Fathiya Al-Murshedi, Abeer Al-Saegh, Amna Al-Futaisi, Saleh Baawain, Almundher Al-Maawali, Hassan Mirza, Maryam Al-Nabhani, Wafaa Al-Shehhi, Saud Al-Shabibi
مصطلحات موضوعية: Immunology, Fowler syndrome, Biology, Phenotype
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::6f6c386a58a03ebc58a4d7c25aca46a4Test
https://doi.org/10.1111/cge.13838/v2/response1Test -
4
المؤلفون: Abeer Al-Saegh, Amna Al-Futaisi, Saud Al-Shabibi, Hassan Mirza, Maryam Al-Nabhani, Wafaa Al-Shehhi, Fathiya Al-Murshedi, Saleh Baawain, Almundher Al-Maawali
المصدر: Clinical genetics. 98(5)
مصطلحات موضوعية: Adult, Male, 2019-20 coronavirus outbreak, Coronavirus disease 2019 (COVID-19), Adolescent, business.industry, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Fowler syndrome, Membrane Transport Proteins, Virology, Phenotype, Hydranencephaly, Young Adult, Child, Preschool, Genetics, Medicine, Humans, Receptors, Virus, Female, Genetic Predisposition to Disease, business, Child, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d70a65d8ccd97817ac44f8e5b09a542Test
https://pubmed.ncbi.nlm.nih.gov/32901920Test -
5
المؤلفون: Almundher Al-Maawali, Roshan Koul, Ahlam Gabr, Alaa Elmanzalawy, Maryam Al-Nabhani, Fathiya Al Murshedi, Naema Al Shibli
المصدر: J Pediatr Genet
مصطلحات موضوعية: 0303 health sciences, Pathology, medicine.medical_specialty, business.industry, 030305 genetics & heredity, Sensory system, medicine.disease, Corpus callosum, Hypotonia, 03 medical and health sciences, 0302 clinical medicine, Peripheral neuropathy, nervous system, Pediatrics, Perinatology and Child Health, Intellectual disability, medicine, medicine.symptom, Agenesis of the corpus callosum, business, Andermann syndrome, 030217 neurology & neurosurgery, Genetics (clinical), Exome sequencing
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c432fdb36888d18ee3429dc41a52a092Test
https://europepmc.org/articles/PMC7396463Test/ -
6دورية أكاديمية
المؤلفون: Mansour S Al-moundhri, Ikram A Burney, Medical Oncology, Manal Al-khanbashi Maryam Al-nabhani
المساهمون: The Pennsylvania State University CiteSeerX Archives
مصطلحات موضوعية: Key words, Gastric cancer
وصف الملف: application/pdf
-
7
المؤلفون: Ghalia Al-Kasbi, Niranjan Joshi, Abdullah Al Farqani, Almundher Al-Maawali, Maryam Al-Nabhani, Khalfan Al Senaidi, Khalid Al-Thihli
المصدر: American journal of medical genetics. Part A. 179(7)
مصطلحات موضوعية: 0301 basic medicine, Adult, Cardiomyopathy, Dilated, Male, medicine.medical_specialty, Cardiomyopathy, Gene Expression, Muscle Proteins, 030105 genetics & heredity, 03 medical and health sciences, Consanguinity, Internal medicine, Exome Sequencing, Genetics, Medicine, Humans, Age of Onset, Child, Genetics (clinical), Base Sequence, business.industry, Familial cardiomyopathy, Homozygote, Hypertrophic cardiomyopathy, Infant, Dilated cardiomyopathy, Cardiomyopathy, Hypertrophic, medicine.disease, Phenotype, Pedigree, 030104 developmental biology, Child, Preschool, Cohort, Mutation, Etiology, Cardiology, Left ventricular noncompaction, Female, business, Protein Kinases
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::814082e9e710815a7370819c6ddde59fTest
https://pubmed.ncbi.nlm.nih.gov/31074094Test -
8
المؤلفون: Fahad Zadjali, Almundher Al-Maawali, Arunodaya R. Gujjar, Saif Al-Mubaihsi, Sameer Raniga, Aida Al-Yahyaee, Maryam Al-Nabhani
المصدر: Human mutation. 39(10)
مصطلحات موضوعية: 0301 basic medicine, Male, Adolescent, Genotype, 030105 genetics & heredity, Biology, medicine.disease_cause, Amino Acyl-tRNA Synthetases, 03 medical and health sciences, chemistry.chemical_compound, Consanguinity, Young Adult, Genetic linkage, Genetics, medicine, Humans, Child, Gene, Genetics (clinical), Exome sequencing, Alleles, Mutation, Aminoacyl tRNA synthetase, Brain, Infant, Phenotype, Pedigree, 030104 developmental biology, FARSB Gene, chemistry, Neurodevelopmental Disorders, Child, Preschool, Transfer RNA, Female, Phenylalanine-tRNA Ligase, Lung Diseases, Interstitial, Tomography, X-Ray Computed
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::786618dc9d0dd80fa6b58e964792b9caTest
https://pubmed.ncbi.nlm.nih.gov/30014610Test -
9
المؤلفون: Fathiya Al-Murshedi, Almundher Al-Maawali, Maryam Al-Nabhani, Amna Al-Futaisi, Abeer Al-Saegh, Samiya Al-Rashdi, Fahad Zadjali, Khalid Al-Thihli, Watfa Al-Mamari, Adila Al-Kindi
المصدر: Clinical genetics. 94(6)
مصطلحات موضوعية: 0301 basic medicine, Male, Candidate gene, Genotype, Computational biology, Biology, DNA sequencing, Novel gene, 03 medical and health sciences, Consanguinity, Intellectual Disability, Intellectual disability, Exome Sequencing, Genetics, medicine, Humans, Exome, Functional studies, Child, Genetics (clinical), Exome sequencing, Alleles, Genetic Databases, Infant, medicine.disease, Pedigree, 030104 developmental biology, Phenotype, Amino Acid Substitution, Child, Preschool, Mutation, Female, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e84d71041311d74941cfe93b5499cdTest
https://pubmed.ncbi.nlm.nih.gov/30125339Test -
10
المؤلفون: Maryam Al-Nabhani, Mansour S. Al-Moundhri, Jennifer A. Rusiecki, Ligong Chen, Andrea A. Baccarelli, Letizia Tarantini
المصدر: Epigenomics. 3:417-429
مصطلحات موضوعية: Cancer Research, Oman, Tumor suppressor gene, Polymerase Chain Reaction, Risk Assessment, CDH1, Antigens, CD, Stomach Neoplasms, Leukocytes, Odds Ratio, Genetics, medicine, Humans, Genes, Tumor Suppressor, Epigenetics, Promoter Regions, Genetic, Cyclin-Dependent Kinase Inhibitor p16, biology, Cancer, Promoter, Sequence Analysis, DNA, Odds ratio, Methylation, DNA Methylation, Cadherins, medicine.disease, Arabs, Neoplasm Proteins, Core Binding Factor Alpha 3 Subunit, Logistic Models, Long Interspersed Nucleotide Elements, Case-Control Studies, DNA methylation, biology.protein, Cancer research, Tumor Suppressor Protein p53
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::505c26428b31e6a16baac2b559ce17baTest
https://doi.org/10.2217/epi.11.65Test