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Iqbal Unnisa Ali

Researcher at National Institutes of Health

Publications -  58
Citations -  4461

Iqbal Unnisa Ali is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Cancer & Gene. The author has an hindex of 32, co-authored 56 publications receiving 4332 citations. Previous affiliations of Iqbal Unnisa Ali include Science Applications International Corporation & University of Karachi.

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Mutational Spectra of PTEN/MMAC1 Gene: a Tumor Suppressor With Lipid Phosphatase Activity

TL;DR: The mutational spectra of the PTEN/MMAC1 gene in tumors from various tissues, especially endometrium, brain, prostate, and ovary, are reviewed, suggesting that depending on the tissue type, the gene appears to be involved in the initiation or the progression of cancers.
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Expression of the vascular permeability factor/vascular endothelial growth factor gene in central nervous system neoplasms.

TL;DR: A significant role for VEGPF is suggested in the development of CNS tumor neovascularity and peritumoral edema and in capillary hemangioblastomas.
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Progress in Cancer chemoprevention : Development of diet-derived chemopreventive agents

TL;DR: Because of their safety and the fact that they are not perceived as "medicine," food-derived products are highly interesting for development as chemopreventive agents that may find widespread, long-term use in populations at normal risk.
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Amplification and/or Overexpression of Platelet-derived Growth Factor Receptors and Epidermal Growth Factor Receptor in Human Glial Tumors

TL;DR: Analysis of genomic organization and expression of platelet-derived growth factor receptors (PDGFR) and epidermal growth factor receptor (EGFR) in human malignant gliomas showed amplification and overexpression of both receptors in distinct subsets of tumors.
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Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

TL;DR: The results presented here demonstrate a loss of heterozygosity of several genes on chromosome 11 in primary breast tumors, and restriction fragment length polymorphism analysis of these DNAs suggests that the most frequent loss of sequences in breast tumors occurs between the beta-globin and parathyroid hormone loci on the short arm of chromosome 11.