Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Moinuddin, Moinuddin"'
Publikováno v:
Pakistan Journal of Medicine and Dentistry, Vol 4, Iss 1 (2024)
Chronic myelogenous leukemia (CML) results from neoplastic transformation of a hematopoietic stem cell. It is cytogenetically characterized by the presence of Philadelphia chromosome which results from reciprocal translocation t(9;22) that juxtaposes
Externí odkaz:
https://doaj.org/article/a4989d7a1e39405e89738e4ec2d2e611
Publikováno v:
Turkish Journal of Hematology, Vol 26, Iss 04, Pp 167-170 (2009)
Objective: Thalassemia is one of the most common genetic disorders worldwide. Cap +1 mutation which causes ‘silent beta thalassemia’ is present around all ethnic groups of Pakistan. This study was designed to detect the frequency of Cap+1 mutatio
Externí odkaz:
https://doaj.org/article/d76a64d34eab4cd787f9b8c82e085fea
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 9, Iss 3, Pp 305-310 (2009)
Objectives: Thalassemia is one of the most common autosomal single-gene disorder worldwide. The highest prevalence of the disease is in the “thalassemia belt” which includes the Mediterranean region, parts of the Middle East, the Indian subcontin
Externí odkaz:
https://doaj.org/article/016ff6d1639d4ba3a9b6dfe417a2ddc6
Autor:
ASHRAF, Shakila1 shakila@squ.edu.om, MOINUDDIN, Moinuddin2
Publikováno v:
UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi. 2015, Vol. 25 Issue 4, p230-235. 6p.
Autor:
Moinuddin Moinuddin, Shakila Ashraf
Publikováno v:
International Journal of Hematology and Oncology. 25:230-235
Thalassemia intermedia lies between asymptomatic β-thalassemia carrier state to severe thalassemia Major. XmnI polymorphism is one of the modifying factors of intermedia phenotype. This study intendeds to determine the frequency of Xmn-I polymorphis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14dd86ba13bb252fa35ea77d901b6be3
https://doi.org/10.4999/uhod.1052
https://doi.org/10.4999/uhod.1052
Publikováno v:
Malaysian Journal of Medical Sciences. Mar-May2013, Vol. 20 Issue 2, p62-66. 5p.
Autor:
Karim, Muhammad Usman Abdul1 staytune1@hotmail.com, Moinuddin, Moinuddin1, Babar, Sadia Usman1
Publikováno v:
Turkish Journal of Hematology. Dec2009, Vol. 26 Issue 4, p167-170. 4p. 1 Black and White Photograph, 1 Chart.
Publikováno v:
Pakistan Journal of Medical Sciences
Background and Objective: Breakpoint cluster region-Abelson (BCR-ABL) rearrangement or Philadelphia (Ph) chromosome in Chronic Myeloid Leukemia (CML) is derived from a reciprocal chromosomal translocation between ABL gene on chromosome 9 and BCR gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e261bfe50c399b9ac1bcea4e9f9caef5
http://europepmc.org/articles/PMC4121711
http://europepmc.org/articles/PMC4121711
Publikováno v:
Pakistan Journal of Medical Sciences
Background and Objective: Co-existence of myeloproliferative disorders (MPD) and Janus associated kinase 2 mutation (JAK2 V617F) is a well-established fact. Only few case reports are available showing presence of JAK2 V617F mutation in chronic myeloi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d86b3855d908cc312db5d08cdf618d62
http://europepmc.org/articles/PMC3955569
http://europepmc.org/articles/PMC3955569
Autor:
Saqib Hussain Ansari, Tasneem Farzana, Mushtaq Ashraf, Mohammed Tahir Khan, Tahir Shamsi, Sajida Erum, Tabassum Mehboob, Saima Munzir, Moinuddin Moinuddin, Kousar Perveen
Publikováno v:
Journal of Pediatric Hematology/Oncology. 35:e153-e156
β-thalassemia is characterized by impaired β-chain synthesis leading to ineffective erythropoiesis, severe anemia, and a need for blood transfusion. Presence of Xmn I polymorphism (-158 C-T nucleotide change) in γ-globin gene is associated with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec024d6650ce378b88a9100f59bc90ae
https://doi.org/10.1097/mph.0b013e31827e8662
https://doi.org/10.1097/mph.0b013e31827e8662