Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Haiam, Abdel Raouf"'
Autor:
Alaaeldin G. Fayez, PhD, Nora N. Esmaiel, PhD, Engy A. Ashaat, MD, Miral M. Refeat, PhD, Randa S. Lotfy, PhD, Haiam Abdel Raouf, PhD, Mona O. El Ruby, MD
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp 1244-1253 (2023)
الملخص: أهداف البحث: عيوب القلب الوعائية وراثية بشكل كبير وحوالي ثلث عيوب القلب الخلقية ناتجة عن عيوب القلب الوعائية. باستخدام التحليل ال
Externí odkaz:
https://doaj.org/article/f6571d0689834dea90a62275742564a8
Autor:
Moushira Zaki, Shams Kholoussi, Somaia Ismail, Haiam Abdel Raouf, Iman Helwa, Naglaa Hassan, Eman Youness, Nadia A. Mohamed, Sanaa Kamal, Walaa Yousef, Mohamed Shaker, Wafaa Ezzat, Yasser A. Elhosary, Omnia M. Saleh, Mona El Gammal, HalaT. El-Bassyouni, Samira Ismail, Mamdouh Bibars, Osama Azmy
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 4, Pp 367-374 (2015)
Background: Polycystic ovary syndrome (PCOS) is the most common endocrine disorder. It is associated with high prevalence of metabolic risk factors, but little is known about the prevalence of metabolic syndrome (MS) and its components among Egyptian
Externí odkaz:
https://doaj.org/article/d2e63bd626be457fb3002fc54774ac59
Autor:
Hala T. El-Bassyouni, Rania Fawzy Mahmoud Abdelkawy, Shams Kholoussi, Khaled H. Hamed, Eman Eissa, Haiam Abdel Raouf
Publikováno v:
Biomedical and Pharmacology Journal. 14:1351-1358
Background: Familial Mediterranean fever (FMF) is an auto inflammatory genetic disease resulted from the mutation of pyrin, which contributes to the formation of inflamma some complex. Therefore, activation of cytokines is one of the hallmarks of FMF
Autor:
Dina A Salah, Iman Helwa, Hala G. Elnady, Haiam Abdel Raouf, Hanan Atta, Assem Metwally Abo-Shanab, Rania Fawzy Mahmoud Abdelkawy
Publikováno v:
Biomedical and Pharmacology Journal. 13:1765-1772
Bronchial asthma (BA) is usually persistent through allergic sensitization, which is likely to result in bronchial hyper-responsiveness and acute bronchoconstriction due to reactions to specific and non-specific trigger stimuli. Many research focused
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 23(9)
In this work, we represented new non-cytotoxic treatments to avoid serious side effects of current used cytotoxic anticancer drugs. These treatments can compensate in finding convenient treatment for each individual case using a single agent from mar
Autor:
Nora N. Esmaiel, Sohair M. Salem, Abeer Ramadan, Haiam Abdel Raouf, Randa I. Khalaf, Alaaeldin Fayez, Hala T. El-Bassyouni, Iman Helwa, Samira Ismaeil, Manal M. Thomas
Publikováno v:
Gene Reports. 14:118-123
Background and objectives The circulating level of growth hormone (GH) is necessary for normal development of skeletal and soft tissues. The growth hormone-1 (GH1) gene is responsible for GH production, any alteration in this gene causes growth hormo
Autor:
Maha Mohamed, Farid Aql, Seham Abd-El Ghafour, Bahget, Naglaa, Kholoussi, Ghada Mohamed El Hossiny, Abdel-Salam, Haiam, Abdel Raouf, Maha, Mohamed Eid, Rania El-Bialy, Esmail
Publikováno v:
International Journal of Molecular and Cellular Medicine
Telomeres are nucleoprotein complexes present at the ends of chromosome to maintain its integrity. Telomere length is maintained by an enzyme called "telomerase". Thus, telomerase activity and telomere length are crucial for the initiation of cancer
Autor:
Sohier A. Maksoud, Heba A. Razik, Naglaa Kholoussi, Amr Kh, Shahera A. Zayed, Somai Ismail, Osman M. Mansour, Raina Kandil, Haiam Abdel Raouf
Publikováno v:
Middle East Journal of Medical Genetics. 5:60-64
Autor:
Hoda H. Fahim, Haiam Abdel Raouf, Refaat Kamel, Wafaa M. Ezzat, Abdelfattah E. Hegazy, Yasser A. Elhosary, Khalda Said Amr
Publikováno v:
Archives of Medical Research. 47:349-355
Activation of telomerase reverse transcriptase (hTERT) has a role in liver carcinogenesis where telomerase is normally suppressed in most human somatic tissues after birth. In the current study we aimed to detect the significance of hTERT mRNA in ear
Autor:
Walaa Yousef, Shams Kholoussi, Moushira Erfan Zaki, Mohamed Shaker, Samira Ismail, Haiam Abdel Raouf, Sanaa M. Kamal, Somaia Ismail, Naglaa M. Hassan, Hala T. El-Bassyouni, Nadia A. Mohamed, Omnia M. Saleh, Mamdouh Bibars, Yasser A. Elhosary, Iman Helwa, Osama Azmy, Mona El Gammal, Eman R. Youness, Wafaa M. Ezzat
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 4, Pp 367-374 (2015)
Egyptian Journal of Medical Human Genetics; Vol 16, No 4 (2015); 367-374
Egyptian Journal of Medical Human Genetics; Vol 16, No 4 (2015); 367-374
Background : Polycystic ovary syndrome (PCOS) is the most common endocrine disorder. It is associated with high prevalence of metabolic risk factors, but little is known about the prevalence of metabolic syndrome (MS) and its components among Egyptia