Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Eman Rabie"'
Autor:
Eman Abdelmohsen Sanad, Howayda Abd El-Hamid El-Shinnawy, Hayam Ahmed Hebah, Dina Aboubakr Farrag, Eman Rabie Anwar Soliman, Mostafa Abdelnasier Abdelgawad
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 58, Iss 1, Pp 1-11 (2022)
Abstract Background Depression is associated with morbidity, death, diminished quality of life, decreased longevity, and even suicidal ideation in hemodialysis patients. Intra-dialytic exercise is considered as integral component of the clinical care
Externí odkaz:
https://doaj.org/article/9aec0ed938b54631adbdedf1f90319ca
Autor:
Kyra L. Feuer, Marah H. Wahbeh, Christian Yovo, Eman Rabie, Anh-Thu N. Lam, Sara Abdollahi, Lindsay J. Young, Bailey Rike, Akul Umamageswaran, Dimitrios Avramopoulos
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-4 (2022)
Abstract Scarless genome editing of induced pluripotent stem cells (iPSCs) is crucial for the precise modeling of genetic disease. Here we present CRISPR Del/Rei, a two-step deletion-reinsertion strategy with high editing efficiency and simple PCR-ba
Externí odkaz:
https://doaj.org/article/f5326552857e4db0aa072037c3580d5b
Autor:
Rabab Khairat, Hanaa El-Karaksy, Hala T. El-Bassyouni, Ahmed K. Saad, Eman Rabie, Khaled Hamed, Noha A. Yassin
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-9 (2022)
Abstract Background Alagille syndrome (ALGS) is a rare autosomal dominant multisystem disorder that affects the liver, heart, eyes, vertebrae, and kidneys and is associated with characteristic facies. This work aimed to study the spectrum of the clin
Externí odkaz:
https://doaj.org/article/e4bad33ceb684f60b95de39dd56dfd05
Autor:
Amr A. Elfattah Hassan Gadalla, Soha M.Abd El-Dayem, Eman Rabie Hassan Fayed, Abo El-Magd Mohamed El-Bohy
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 10:1715-1719
Background: Ultrasound is considered as a suitable, accurate, safe, available technique to measure abdominal adipose tissue of low cost compared to other imaging modalities as CT and MRI. It is superior to BMI as a monitor for diabesity because of it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23d3f55d956f912ccc1072d5c3a4294e
https://doi.org/10.3889/oamjms.2022.9708
https://doi.org/10.3889/oamjms.2022.9708
Autor:
Maha Rashed Abouzaid, Nehal F. Hassib, Hoda Abdalla Ahmed, Mohamed Ahmed Abdel‐Kader, Mostafa I. Mostafa, Mennat I Mehrez, Ghada El-Kamah, Suher Zada, Inas S. M. Sayed, Khalda Amr, Yasmine H. Mohsen, Eman Rabie
Publikováno v:
Genes
Volume 12
Issue 9
Genes, Vol 12, Iss 1389, p 1389 (2021)
Volume 12
Issue 9
Genes, Vol 12, Iss 1389, p 1389 (2021)
Ectodermal dysplasia (ED) is a diverse group of genetic disorders caused by congenital defects of two or more ectodermal-derived body structures, namely, hair, teeth, nails, and some glands, e.g., sweat glands. Molecular pathogenesis of ED involves m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5ba72ef3a5b4aa11737c3a1daf3bd49
Autor:
Alexandros Onoufriadis, Eman Rabie, Frank Po-Chao Chiu, Hagar Nofal, Rania Alakad, Ahmad Alabdulkareem, Rashida Pramanik, Ahmad Nofal, Thithiwat Chaikul
Publikováno v:
Dermatologic therapyREFERENCES. 34(5)
H syndrome is a rare autosomal recessive disorder with clinical features comprising: hyperpigmentation, hypertrichosis, hearing loss, heart anomalies, low height, hypogonadism and hepatosplenomegaly. H syndrome results from loss-of-function mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b406923c5be82a1dd1d3334c6e4eb12
https://pubmed.ncbi.nlm.nih.gov/34351669
https://pubmed.ncbi.nlm.nih.gov/34351669
Autor:
Sanad, Eman Abdelmohsen, El-Shinnawy, Howayda Abd El-Hamid, Hebah, Hayam Ahmed, Farrag, Dina Aboubakr, Soliman, Eman Rabie Anwar, Abdelgawad, Mostafa Abdelnasier
Publikováno v:
Egyptian Journal of Neurology, Psychiatry & Neurosurgery; 10/27/2022, Vol. 58 Issue 1, p1-11, 11p
Publikováno v:
Genes, Vol 12, Iss 295, p 295 (2021)
Genes
Volume 12
Issue 2
Genes
Volume 12
Issue 2
Xeroderma pigmentosum is a rare autosomal recessive skin disorder characterized by freckle-like dry pigmented skin, photosensitivity, and photophobia. Skin and ocular symptoms are confined to sun exposed areas of the body. Patients have markedly incr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3cc3f99c515289c4ab35bf7b7b0c338
https://www.mdpi.com/2073-4425/12/2/295
https://www.mdpi.com/2073-4425/12/2/295
Autor:
Marah H. Wahbeh, Kyra L. Feuer, Christian Yovo, Eman Rabie, Anh-Thu N. Lam, Sara Abdollahi, Lindsay J. Young, Bailey Rike, Akul Umamageswaran, Dimitrios Avramopoulos
Scarless genome editing is an important tool for the accurate recapitulation of genetic variation in human disease models. Various CRISPR/Cas9-based scarless editing methods have been reported. However, some of these methods have low editing efficien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97643a0c4d0014ba815ca67bf0023d49
https://doi.org/10.1101/2021.01.18.427163
https://doi.org/10.1101/2021.01.18.427163
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Background Hemophilia A (HA) is an inherited X‐linked recessive coagulation disorder caused by factor VIII (F8) deficiency. F8 rearrangements involving intron 22 (int22) and intron 1 (int1) account for almost half of severe HA phenotype also a hots
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f26992febc0f6c0d89e308a1b990e1a
https://doi.org/10.1002/mgg3.1575
https://doi.org/10.1002/mgg3.1575