Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lubna M. Desouky"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-8 (2022)
Abstract Background Recent research proposed an association between functional defects involving CHEK2 I157T and SULT1A1 R213H variants and increased incidence of several types of cancer. A total of 86 unrelated colorectal cancer patients attending t
Externí odkaz:
https://doaj.org/article/3fd2e300589f418186d718348aee7d07
Autor:
Mohamed S. Abdel-Hamid, Mahmoud Y. Issa, Laila K. Effat, Maha S. Zaki, Lubna M. Desouky, Sherif F. Abdel‐Ghafar, Suzan R. Ismail
Publikováno v:
Clinical Genetics. 98:445-456
Micro and Martsolf syndromes are rare clinically and genetically overlapping disorders caused by mutations in RAB3GAP1, RAB3GAP2, RAB18 and TBC1D20 genes. We describe 34 new patients, 27 with Micro and 7 with Martsolf. Patients presented with the cha
Autor:
Ragaa A Ramadan, Ebtesam M. Abdalla, Mostafa Elnaggar, Mai Moaaz, Mohamed Selima, Mohamed Samir, Lubna M. Desouky
Publikováno v:
Meta Gene. 11:209-216
Variants of vitamin D receptor (VDR) and toll like receptors (TLR) have been investigated in relation to colon cancer (CC) susceptibility, however results were always inconsistent. Methods: We examined the association of CC risk with four variants VD
Autor:
Marwa A. Madkour, Moyassar Ahmad Zaki, Karim Mahmoud Nabil Mohamed Kamel, Rania Mohamed El Sharkawy, Ragaa Abelkader Ramadan, Lubna M. Desouky
Publikováno v:
Journal of Diabetes Mellitus. :1-9
Objectives: Diabetic retinopathy (DR) is one of the most common microvascular complications of type 2 diabetes mellitus (T2DM). It is multifactorial with the contribution of multiple genetic factors. We questioned the association of polymorphisms in
Autor:
Ragaa A Ramadan, Mai Moaaz, Lubna M. Desouky, Mostafa Elnaggar, Ebtesam M. Abdalla, Mohamed Selima, Mohamed Samir
Publikováno v:
Meta Gene. 17:S22
Variants of vitamin D receptor (VDR) and toll like receptors (TLR) have been investigated in relation to colon cancer (CC) susceptibility, however results were always inconsistent. Methods We examined the association of CC risk with four variants VDR