Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sabita K. Murthy"'
Autor:
Stylianos E. Antonarakis, Mahmoud Taleb Al-Ali, Samuel Deutsch, Sabita K. Murthy, Najib Al-Khaja, Sarah Al-Hajali, Armand Bottani, Uppala Radhakrishna, Mohammed Naveed, Swapan K. Nath
Publikováno v:
American Journal of Medical Genetics. A, Vol. 140, No 13 (2006) pp. 1440-1446
Ectrodactyly with aplasia of long bones syndrome is one of the most recognizable defects involving the extremities. We have studied a very large eight-generation consanguineous Arab family from the United Arab Emirates (UAE) with multiple severe limb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6418a8deef82a857d9f1c5b0f7d72b56
https://doi.org/10.1002/ajmg.a.31239
https://doi.org/10.1002/ajmg.a.31239
Autor:
Gudrun Amann, Jonathan M. Lee, Meredith Wernick, Joe W. Gray, Sabita K. Murthy, Lisa A. Porter, Nisha Anand, Colin Collins, Joachim Diebold, Doug J. Demetrick, I. Howard Cukier
Publikováno v:
Biological Sciences Publications
We have found that EEF1A2, the gene encoding protein elongation factor EEF1A2 (also known as eEF-1 alpha 2), is amplified in 25% of primary ovarian tumors and is highly expressed in approximately 30% of ovarian tumors and established cell lines. We h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97e16d78c3a89555794a355a26b2c648
https://doi.org/10.1038/ng904
https://doi.org/10.1038/ng904
Autor:
Sabita K. Murthy, Michael A. Walter, J. S. Friedman, Doug J. Demetrick, Robert J. Winkfein, Joseph Tucker, Paul P. M. Schnetkamp
Publikováno v:
Human Genetics. 103:411-414
The retinal rod Na-Ca+K exchanger is a unique calcium extrusion protein found only in the outer segments of retinal rod photoreceptors. Rod Na-Ca+K exchanger cDNA (NCKX1) has been cloned from bovine and human retinas. Here, we have used fluorescent i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5594e9a9cc2684df0b15134dd0243ad0
https://doi.org/10.1007/s004390050842
https://doi.org/10.1007/s004390050842
Autor:
Sabita K. Murthy, K. Prabhakara
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 331:175-180
Hyperthermic induction of chromosomal aberrations was examined in human lymphocytes. For this purpose, whole blood cultures were exposed to an elevated temperature (43 degrees C) at the 46th h of culture initiation, followed by 24 h of recovery. Deta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77cdab571f0d781ab5ee486c61a0c8dc
https://doi.org/10.1016/0027-5107(95)00066-r
https://doi.org/10.1016/0027-5107(95)00066-r
Autor:
Sabita K, Murthy, Douglas J, Demetrick
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 319
Fluorescence in situ hybridization (FISH) is a nonisotopic labeling and detection method that provides a direct way to determine the relative location or copy number of specific DNA sequences in nuclei or chromosomes. With recent advancements, this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b7ba00ff72291165a2cddf364c14628
https://pubmed.ncbi.nlm.nih.gov/16719359
https://pubmed.ncbi.nlm.nih.gov/16719359
Autor:
Douglas J. Demetrick, Sabita K. Murthy
Publikováno v:
Cell Imaging Techniques ISBN: 9781588291578
Fluorescence in situ hybridization (FISH) is a nonisotopic labeling and detection method that provides a direct way to determine the relative location or copy number of specific DNA sequences in nuclei or chromosomes. With recent advancements, this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65a039866ffda62a41fce07b6a629585
https://doi.org/10.1007/978-1-59259-993-6_12
https://doi.org/10.1007/978-1-59259-993-6_12
Autor:
Sabita K. Murthy, Eman Essa Mohd Al-Rowaished, Maryam Essa A. Shara, Mahmoud Taleb Al-Ali, Ashok K. Malhotra, Sehba Naveed, Sara Mani, Abdulla Ibrahim AlKhayat
Publikováno v:
Medical principles and practice : international journal of the Kuwait University, Health Science Centre. 16(1)
Objective: To describe incidence of Down syndrome in Dubai, United Arab Emirates (UAE). Subjects and Methods: A total of 63,398 newborn babies in Dubai (24,250 UAE nationals and 39,148 non-UAE) during a 5-year period of 1999–2003 were routinely exa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ef461b892cac90b8c75944348da3be6
https://pubmed.ncbi.nlm.nih.gov/17159360
https://pubmed.ncbi.nlm.nih.gov/17159360
Publikováno v:
Archives of pathologylaboratory medicine. 129(1)
Context.—The Topoisomerase IIα (TOP2A) protein is the target of the anthracycline class of chemotherapeutic agents. TOP2A is frequently coamplified with c-erb-B2 and consequently might be a prognostic and/or predictive factor for breast cancer pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32021e18b2026dde59a2a0540c28993e
https://pubmed.ncbi.nlm.nih.gov/15628907
https://pubmed.ncbi.nlm.nih.gov/15628907
Autor:
Clemens F M, Prinsen, Conan B, Cooper, Robert T, Szerencsei, Sabita K, Murthy, Douglas J, Demetrick, Paul P M, Schnetkamp
Publikováno v:
Advances in experimental medicine and biology. 514
The past few years has seen significant progress in our understanding of the retinal rod and cone Na+/Ca2+-K+ exchanger (NCKX) genes. The human rod and cone NCKX genes were localized to chromosomes 15q22 and 9p22, respectively. In situ hybridization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cad8779082087271a33ececebe3689e2
https://pubmed.ncbi.nlm.nih.gov/12596925
https://pubmed.ncbi.nlm.nih.gov/12596925
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 15(12)
Loss of heterozygosity is commonly assumed to be due to deletion of the appropriate genomic region in one chromosome within a neoplastic cell but may be due to other mechanisms such as mitotic non-disjunction or somatic recombination leading to unipa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd9171612cf938b02465d31cfb8de175
https://pubmed.ncbi.nlm.nih.gov/12481003
https://pubmed.ncbi.nlm.nih.gov/12481003