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Indentification of C-kit exon 11 mutations and prognostic imortance in acute myeloid leukemia (AML) patients from Pakistan (Record no. 21870)

MARC details
000 -LEADER
fixed length control field 02435nam a22001697a 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20221018164512.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 221018b ||||| |||| 00| 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number hbk
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 591
Item number Id26
100 ## - MAIN ENTRY--PERSONAL NAME
Student name Sana Akbar,
Class BS Zoology,
Session 2015-2019,
Supervisor Supervised by Dr. Afia M. Akram
245 ## - TITLE STATEMENT
Title Indentification of C-kit exon 11 mutations and prognostic imortance in acute myeloid leukemia (AML) patients from Pakistan
Statement of responsibility, etc / Sana Akbar
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Lahore :
Name of publisher, distributor, etc Division of Science & Technology, University of Education,
Date of publication, distribution, etc 2019
300 ## - PHYSICAL DESCRIPTION
Extent xiii, 58 p.
Accompanying material CD
520 ## - SUMMARY, ETC.
Summary, etc Leukemia is designated as abnormal division of blood cells. Blood cells begin to proliferate<br/>abnormally and fail to differentiate into normal cells. Acute myeloid leukemia is a<br/>heterogeneous disorder characterized by abnormal proliferation and immature production of<br/>hematopoietic stem cells. Major causes of AML might be mutations, translocations or any<br/>chromosomal abnormality. C-kit is a proto oncogene which is related to Receptor Tyrosine<br/>Kinase family and have a significant influence on cell proliferation, maturation and survival.<br/>Exon 11 of c-kit gene is sequenced and analyzed to study its prognosis and role in AML among<br/>Pakistani patients. Aim of this study are to focus on hematological (blast cells percentage,<br/>TLCs, hemoglobin level etc.) and clinical parameters (hepatomegaly, splenomegaly, FAB<br/>classification etc.) associated with mutation in exon 11 of c-kit gene and its prognosis.<br/>Mutations in exon 11 of c-kit gene are studied by polymerase chain reaction (PCR) and Sanger<br/>sequencing technique in current investigations. All sequences are studied by genius prime 2019<br/>and statistically analyzed by Chi square Fischer’s exact test. Two out of 31 patients of AML<br/>are observed having mutation in this exon at codon 555. Both patients have same mutation<br/>resulted glutamic acid in place of valine. Mutations in exon 11 of c-kit gene are only found<br/>associated with cytogenetic, statistically. However all other parameters are not significantly<br/>associated with this exon and have p value higher than 0.05. Prognostic implications of c-kit<br/>are still unclear. However, mutations RTK have poor influence on outcome. These findings<br/>helped us to study prognosis of c-kit and its association with hematological and clinical<br/>parameters among AML patients.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Zoology--Acute Myeloid--Leukemia--Patients--Pakistan
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Theses
Holdings
Withdrawn status Damaged status Home library Current library Date acquired Full call number Barcode Date last seen Price effective from Koha item type
    UE-Central Library UE-Central Library 18.10.2022 591 Id26 TTH180 18.10.2022 18.10.2022 Theses
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