Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Harem Othman Smail"'
Autor:
Harem Othman Smail
Publikováno v:
Kurdistan Journal of Applied Research, Vol 9, Iss 2 (2024)
The primary epigenetic alteration is DNA methylation. This study examined variations in DNA methylation in patients with type 2 diabetes at various time intervals, concentrating on the Calpain-10 (CAPN10), ATP binding cassette subfamily C member 8 (A
Externí odkaz:
https://doaj.org/article/2dfa1a0205614e4e8590cb5a22142b41
Publikováno v:
Journal of Experimental and Molecular Biology (2024)
The purpose of the experiment was to investigate onion (Allium cepa) root growth, cell division, and mitotic index. The onions were placed into four different water samples (Control water, Azadi bridge, Sar Razan, and Sar Baskan) for 72 hours in beak
Externí odkaz:
https://doaj.org/article/5c9abef8b2d04e6b8771acf11188dbe7
Autor:
Harem Othman Smail
Publikováno v:
Polytechnic, Vol 13, Iss 2, Pp 23-27 (2023)
Micronuclei in lymphocytes can indicate DNA damage or chromosomal instability. This study aimed to compare the Micronuclei to the different period diagnoses of type 2 diabetes mellitus. Four groups were created out of 140 people: type 2 diabetes mell
Externí odkaz:
https://doaj.org/article/885a6f7756ce43c390511e83f9717728
Autor:
Harem Othman Smail
Publikováno v:
Biology, Medicine & Natural Product Chemistry, Vol 12, Iss 1, Pp 45-53 (2022)
The review aimed to understand and explain the association between some major endocrine conditions and COVID-19. Since March 2019, COVID-19 has been identified as a pandemic by the World Health Organization (WHO) and has infected millions of individu
Externí odkaz:
https://doaj.org/article/2466ebd0be4a4955b656bb6ac7b43395
Autor:
Harem Othman smail
Publikováno v:
Journal of Experimental and Molecular Biology (2023)
This analysis aimed to clarify the molecular basis of fragile X syndrome and explain the role of genetic material in the genetic disease's development and treatment. Fragile X syndrome is an X-linked mutation inheritance disorder. The mutated gene is
Externí odkaz:
https://doaj.org/article/6ac3e6740fbe4f74aa7dc6f9b2655a22
Autor:
Harem Othman Smail
Publikováno v:
Biology, Medicine & Natural Product Chemistry, Vol 11, Iss 1, Pp 45-54 (2022)
This paper aimed to understand and compare the two popular cytogenetic techniques of fluorescence in situ hybridization (FISH) and comparative genomic hybridization (CGH) in detecting breast cancer chromosomal abnormality. Several chromosomal anomali
Externí odkaz:
https://doaj.org/article/84234b7f402d49e280de418632729f4c
Autor:
Harem Othman smail
Publikováno v:
Journal of Experimental and Molecular Biology (2023)
From this review, I discussed the epigenetics of panic disorder .epigenetic is the changes in the heritable phenotype without any change from the DNA sequence. The roles of different types of epigenetics (DNA methylation and chromatin remodeling) hav
Externí odkaz:
https://doaj.org/article/14c04eaf969848f7be4a197d82dea6bc
Autor:
Harem Othman Smail
Publikováno v:
Biology, Medicine & Natural Product Chemistry, Vol 9, Iss 2, Pp 57-64 (2020)
The main aims of this review were to understand the roles of gene therapy in the treatment and prevention of type 1 diabetes mellitus and I will discuss a brief history, approaches, vector types with the future of diabetes following clinical use. Typ
Externí odkaz:
https://doaj.org/article/59c9d09c680a4becbbbc0cd170b379e4
Autor:
Harem Othman Smail
Publikováno v:
AIMS Genetics, Vol 6, Iss 4, Pp 88-97 (2019)
The aims of this review were to understand the roles of bitter taste genes in humans. Some of the peoples have the capacity to taste some chemical substance such as phenylthiocarbamide (PTC) while others cant not based on the dietary hazards and food
Externí odkaz:
https://doaj.org/article/a1b3c225829341b99d4e1cb983bd4a14
Autor:
Harem Othman Smail
Publikováno v:
AIMS Genetics, Vol 6, Iss 3, Pp 36-45 (2019)
The objectives of this review were once to understand the roles of the epigenetics mechanism in different types of diabetes, obesity, overweight, and cardiovascular disease. Epigenetics represents a phenomenon of change heritable phenotypic expressio
Externí odkaz:
https://doaj.org/article/14c0c18e71b445e9888878776a6f2c64