Zobrazeno 1 - 10
of 215
pro vyhledávání: '"Khaled K Abu Amero"'
Autor:
Deepak P Edward, Hind Alkatan, Qundeel Rafiq, Charles Eberhart, Saleh Al Mesfer, Nicola Ghazi, Leen Al Safieh, Altaf A Kondkar, Khaled K Abu Amero
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0121706 (2015)
To study the differential expression of microRNA (miRNA) profiles between intraocular medulloepithelioma (ME) and normal control tissue (CT).Total RNA was extracted from formalin fixed paraffin embedded (FFPE) intraocular ME (n=7) and from age matche
Externí odkaz:
https://doaj.org/article/1a34181cd3af42e3875fed6be71420ee
Autor:
Altaf A. Kondkar, Tahira Sultan, Faisal A. Almobarak, Hatem Kalantan, Khaled K. Abu-Amero, Saleh A. Al-Obeidan
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Objective Plexin domain containing 2 (PLXDC2), a cell surface transmembrane protein receptor for pigment epithelium derived factor, is expressed in many tissues including the eye. Polymorphism rs7081455 flanking PLXDC2 has been associated wi
Externí odkaz:
https://doaj.org/article/2f2b8ed72624411e89063c53d65fcf55
Publikováno v:
BMC Evolutionary Biology, Vol 18, Iss 1, Pp 1-16 (2018)
Abstract Background The main unequivocal conclusion after three decades of phylogeographic mtDNA studies is the African origin of all extant modern humans. In addition, a southern coastal route has been argued for to explain the Eurasian colonization
Externí odkaz:
https://doaj.org/article/2977e50a374c4b76a5f83021a54dbe2a
Autor:
Hatem Kalantan, Altaf A. Kondkar, Tahira Sultan, Taif A. Azad, Nasser A. Alsabaani, Masoud Ali AlQahtani, Abdulrahman Almummar, Yuato Liu, Khaled K. Abu-Amero
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
Abstract Objective Polymorphism rs13334190 in the zinc finger protein 469 gene has been suggested to predispose toward a “thin” cornea, which then becomes keratoconic or is directly pathogenic. Thus, we genotyped polymorphism rs13334190 in 127 un
Externí odkaz:
https://doaj.org/article/ebf438a316274aba9bfbac5d19fb4169
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
Abstract Objective Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is known to be caused by mutations in KIF21A or TUBB3 or other known genes (SALL4, CHN1, HOXA1). However, affected children may harbor other genetic defects. Therefore,
Externí odkaz:
https://doaj.org/article/8db5309e3fbc4b679aed28169ceac2ef
Publikováno v:
BMC Evolutionary Biology, Vol 17, Iss 1, Pp 1-15 (2017)
Abstract Background The colonization of Eurasia and Australasia by African modern humans has been explained, nearly unanimously, as the result of a quick southern coastal dispersal route through the Arabian Peninsula, the Indian subcontinent, and the
Externí odkaz:
https://doaj.org/article/81fe4aec944448e1b0445a5085019b73
Autor:
Khaled K. Abu-Amero, Khaled S. Al-Hadyan, Nasser M. Al-Rajhi, Medhat M. El-Sebaie, Najla M. Al-Harbi, Ghazi A. Alsbeih
Purpose: Mitochondria and ionizing radiation overlap in a number of features; for instance, both generate harmful reactive oxygen species, and that radiation can induce cell death through the intermediary of mitochondria. Because a number of genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::459000997db8afd15c3c7f672fe097b9
https://doi.org/10.1158/1078-0432.c.6517662
https://doi.org/10.1158/1078-0432.c.6517662
Autor:
Khaled K. Abu-Amero, Khaled S. Al-Hadyan, Nasser M. Al-Rajhi, Medhat M. El-Sebaie, Najla M. Al-Harbi, Ghazi A. Alsbeih
Supplementary Data from Involvement of Mitochondrial DNA Sequence Variations and Respiratory Activity in Late Complications following Radiotherapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35bf37df467fef5177f381f081c02def
https://doi.org/10.1158/1078-0432.22440315.v1
https://doi.org/10.1158/1078-0432.22440315.v1
Publikováno v:
Pediatrics and Neonatology, Vol 56, Iss 6, Pp 393-401 (2015)
Data on the pattern of epilepsy caused by metabolic disorders in the first 2 years of life are limited in developing countries. We aimed to identify the metabolic causes of epilepsy presented in the first 2 years of life and to describe their clinica
Externí odkaz:
https://doaj.org/article/c2ae704037d84f878bbe32aa8cce45c0
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0129839 (2015)
The modern human colonization of Eurasia and Australia is mostly explained by a single-out-of-Africa exit following a southern coastal route throughout Arabia and India. However, dispersal across the Levant would better explain the introgression with
Externí odkaz:
https://doaj.org/article/42a0e79ff63c4d1698e384edc9e6d070