Zobrazeno 1 - 10 of 11 pro vyhledávání: '"Sana Al-Jarrash"'
1
Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients
Autor: Sana Al-Jarrash, J. Francis Borgio, Zaki A. Naserullah, Sayed AbdulAzeez, Ahmed M. Al-Suliman, Huda I. ElFakharay, Noor B. Almandil
Publikováno v: Molecular Biology Reports. 47:603-606
In the Eastern province of Saudi Arabia, thalassemia is highly common. Data on the effect of alpha globin gene variation on the concentration of iron on transfusion dependent Saudis are scanty. A total of 166 transfusions dependent β-thalassemia wer
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc7c19f77e0b5ee5390ff3076f8400a
https://doi.org/10.1007/s11033-019-05168-w
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3
KLF1 gene and borderline hemoglobin A2 in Saudi population
Autor: Sayed AbdulAzeez, Amein K. Al-Ali, J. Francis Borgio, Ahmed M. Al-Muslami, Ahmed M. Al-Suliman, Mohammed S. Al-Madan, Zaki A. Naserullah, Sana Al-Jarrash
Publikováno v: Archives of Medical Science : AMS
Introduction Elevated HbA2 (hemoglobin A2) level is considered the most reliable hematological parameter for the detection of β-thalassemia carriers. However, some carriers are difficult to recognize because the level of HbA2 is not in the distincti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d08d1f53553cae59b0e1da3b05e7df7
http://europepmc.org/articles/PMC5778434
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5
Hemoglobin A
Autor: Amani M, Al-Amodi, Neda Z, Ghanem, Sumayh A, Aldakeel, Lubna, Ibrahim Al Asoom, Nazish, Rafique Ahmed, Noor B, Almandil, Zaki A, Naserullah, Sana, Al-Jarrash, Mohammed, Shakil Akhtar, Sayed, AbdulAzeez, Amein K, Al-Ali, J Francis, Borgio
Publikováno v: Current medical research and opinion. 34(5)
Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin AThe widely used high performance liquid chromatography (Variant II Bio-Rad) was used to measure HbAOut of 288 samples, 96 had HBB gene mutations
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f726f703f11018fbf837f3d2f5f4e097
https://pubmed.ncbi.nlm.nih.gov/29383950
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6
The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population
Autor: Fatimah Alabdrabalnabi, Amein Al Ali, Mohammed Shakil Akhtar, Jesu Francis Borgio, Noor B. Almandil, Sayed AbdulAzeez, Huda I. ElFakharay, Hatem O. Qutub, Ahmed Suliman, Mohammed A. AlKhalifah, Fuad Qaw, Zaki A. Naserullah, Sana Al Jarrash
Publikováno v: Molecular medicine reports. 17(1)
The regions of Al‑Qatif and Al‑Ahssa in the Eastern Province of Saudi Arabia are known for their high prevalence of hemoglobinopathies, including β‑thalassemia and sickle cell anemia. Previously, the α‑gene deletion has been demonstrated as
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2e9fe401d098a6f1f39fc154cfe4c32
https://pubmed.ncbi.nlm.nih.gov/29138844
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7
Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi β-Thalassemia Patients
Autor: Ahmed Sulaiman, Hatem O. Qutub, Zaki Nasserullah, Alhusain J. Alzahrani, Martin H. Steinberg, Sana Al Jarrash, Cyril Cyrus, Shahanas Chathoth, Chittibabu Vatte, Hassan Alsaleem, J. Francis Borgio, Amein Al Ali, Abdullah M. Al-Rubaish
Publikováno v: BioMed Research International
BioMed Research International, Vol 2017 (2017)
Background and Objectives.β-Thalassemia and sickle cell disease are genetic disorders characterized by reduced and abnormalβ-globin chain production, respectively. The elevation of fetal hemoglobin (HbF) can ameliorate the severity of these disorde
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b6b06b8c8761da177ad639cdb2fb5f
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8
Spectrum ofα-Thalassemia Mutations in Transfusion-Dependent β-Thalassemia Patients from the Eastern Province of Saudi Arabia
Autor: Sana Al-Jarrash, Waleed H. Albuali, Amein K. Al-Ali, Mohammed Shakil Akhtar, J. Francis Borgio, Zaki Nasserullah, Ahmed Suliman, Fuad Qaw
Publikováno v: Hemoglobin. 37:65-73
Both α- and β-thalassemia (α- and β-thal) are highly prevalent in the population of the Al-Qatif and Al-Ahsa regions in the Eastern Province of Saudi Arabia. This study provides a more precise picture of the α-thal mutations prevalent in 104 tra
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcff58985371c28dd692262ce4077990
https://doi.org/10.3109/03630269.2012.753510
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10
Co-inheritance of novel ATRX gene mutation and globin (αβ) gene mutations in transfusion dependent beta-thalassemia patients
Autor: Fuad Qaw, J. Francis Borgio, Mohammed S. Al-Madan, Rudaynah A. Alali, Fahad Al-Muhanna, Sana Al-Jarrash, Amein K. Al-Ali, Martin H. Steinberg, Mohammed A. AlKhalifah, Awatif N. Al-Nafie, Sayed AbdulAzeez, Ahmed M. Al-Suliman, Zaki A. Naserullah
Publikováno v: Blood cells, moleculesdiseases. 55(1)
α-Thalassemia X-linked mental retardation syndrome is a rare inherited intellectual disability disorder due to mutations in the ATRX gene. In our previous study of the prevalence of β-thalassemia mutations in the Eastern Province of Saudi Arabia, w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc27db39431d943a3cbcdea8d3a77ab8
https://pubmed.ncbi.nlm.nih.gov/25976463
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