Effect of natural PAL-enzyme on the quality of egg white and mushroom flour and study its impact on the expression of PKU related genes and phenylalanine reduction in mice fed on

Autor: Hesham A. Eissa, Zeinab Y. Abdallah, Wagdy K.B. Khalil, Wafaa A. Ibrahim, Hoda F. Booles, Mahrousa M. Hassanane

Publikováno v: Journal of Genetic Engineering and Biotechnology, Vol 15, Iss 2, Pp 443-451 (2017)

PKU patients react to therapy with a low phenylalanine diet, but adherence to this diet is troublesome, subsequently the expansion of alternative ways is demand. Phenylalanine ammonia lyase (PAL) is one of this ways, which converts phenylalanine to h

Externí odkaz: https://doaj.org/article/9e95dc4b16d7457094c5094b819f334b

Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses

Autor: Khaled R. Gaber, Mona M. Ibrahim, Mona K. Farag, Zeinab Y. Abdallah, Sara H. Eldessouky, Ekram M. Fateen

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 159-163 (2015)

Background: Mucopolysaccharidoses (MPS) are autosomal recessive disorders characterized by deficiency of lysosomal enzymes which break down the glycosaminoglycans (GAGs) which results in widespread intra and extra-cellular accumulations of GAGs. Earl

Externí odkaz: https://doaj.org/article/2155c438ea20460e8c30953690f0030b

Clinical Implications of S100A12 and Resolvin D1 Serum Levels, and Related Genes in Children with Familial Mediterranean Fever

Autor: Hisham Megahed, Mona Ibrahim, Ghada Nour Eldeen, Mohamed Fares, Hala T. El-Bassyouni, Zeinab Y. Abdallah, Khaled H. Hamed, Mahmoud ElHefnawi, Manal M. Thomas

Publikováno v: Journal of Child Science. 11:e163-e169

The aim of this article was to study the role of S100A12 and resolvin D1-related genes and serum levels in the diagnosis and detection of subclinical inflammation in children with familial Mediterranean fever (FMF) during the quiescent stage of the d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::37a12367cbd9b753d07eb90beb3197a4
https://doi.org/10.1055/s-0041-1731303

Fifteen years experience: Egyptian metabolic lab

Autor: Amr Gouda, Ashraf Tabll, Zeinab y. Abdallah, Ekram Fateen, Mona Ibrahim

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 15, Iss 4, Pp 379-385 (2014)

Background Inborn errors of metabolism (IEM) are single gene disorders responsible for abnormalities in the synthesis or catabolism of proteins, carbohydrates and fats by means of defective enzymes or transport proteins which results in a block of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d951a6684e9d20722ffcabef15f9d7de
http://www.sciencedirect.com/science/article/pii/S1110863014000834

Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses

Autor: Ekram M. Fateen, Sara H. El‐Dessouky, Zeinab Y. Abdallah, Mona K. Farag, Khaled R. Gaber, Mona M. Ibrahim

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 159-163 (2015)
Egyptian Journal of Medical Human Genetics; Vol 16, No 2 (2015); 159-163

Background : Mucopolysaccharidoses (MPS) are autosomal recessive disorders characterized by deficiency of lysosomal enzymes which break down the glycosaminoglycans (GAGs) which results in widespread intra and extra-cellular accumulations of GAGs. Ear

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9388584624311c253cc1e6bcac0c6e