Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fatimah A. Nahhas"'
Autor:
Michael A. Tainsky, Sorin Draghici, Judith Abrams, Gerard Tromp, Natalie N. Shirley, Nancy K. Levin, Robert Morris, Adnan Munkarah, David Fishman, Steven S. Witkin, Karen Lu, Fatimah A. Nahhas, Bin Ye, James Nowak, Xiaoju Wang, Rouba Ali-Fehmi, Gagandeep Bawa, Alexei Ionan, Saroj Mohapatra, Madhumita Chatterjee
A noninvasive screening test would significantly facilitate early detection of epithelial ovarian cancer. This study used a combination of high-throughput selection and array-based serologic detection of many antigens indicative of the presence of ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b12f6ef30bbfa0e60fcdda9f5b882c6
https://doi.org/10.1158/0008-5472.c.6495291
https://doi.org/10.1158/0008-5472.c.6495291
Autor:
Michael A. Tainsky, Sorin Draghici, Judith Abrams, Gerard Tromp, Natalie N. Shirley, Nancy K. Levin, Robert Morris, Adnan Munkarah, David Fishman, Steven S. Witkin, Karen Lu, Fatimah A. Nahhas, Bin Ye, James Nowak, Xiaoju Wang, Rouba Ali-Fehmi, Gagandeep Bawa, Alexei Ionan, Saroj Mohapatra, Madhumita Chatterjee
Supplementary Tables 1-4 from Diagnostic Markers of Ovarian Cancer by High-Throughput Antigen Cloning and Detection on Arrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11d85a240fe57ee599997d3f18c8a7b6
https://doi.org/10.1158/0008-5472.22366788.v1
https://doi.org/10.1158/0008-5472.22366788.v1
Autor:
Fatimah A. Nahhas, Linda Spencer, Allison Jay, Barry Wolf, Robert L. Conway, Gerald L. Feldman
Publikováno v:
Genetics in Medicine. 17:205-209
Biotinidase deficiency, if untreated, usually results in neurological and cutaneous symptoms. Biotin supplementation markedly improves and likely prevents symptoms in those treated early. All states in the United States and many countries perform new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b687108f180bf503d3a59e397b7de6e1
https://doi.org/10.1038/gim.2014.104
https://doi.org/10.1038/gim.2014.104
Publikováno v:
The Journal of Molecular Diagnostics. 16:689-696
Triple-primed PCR assays have become the preferred fragile X syndrome testing method. Using a commercially available assay, we detected a reproducible extra peak(s) in 0.5% of 13,161 clinical samples. The objectives of this study were to determine th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7274bbfacdb3952419d6cf8e3a97022f
https://doi.org/10.1016/j.jmoldx.2014.06.006
https://doi.org/10.1016/j.jmoldx.2014.06.006
Autor:
L. Spencer, J. Miller, A. Fribley, Robert L. Conway, Gerald L. Feldman, H. Li, Fatimah A. Nahhas, Barry Wolf
Publikováno v:
Molecular Genetics and Metabolism. 112:242-246
Biotinidase deficiency (BD) is an autosomal recessive disorder resulting in the inability to recycle the vitamin biotin. Individuals with biotinidase deficiency can develop neurological and cutaneous symptoms if they are not treated with biotin. To d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd75ef20d961e8776596892bbfe87fb0
https://doi.org/10.1016/j.ymgme.2014.04.002
https://doi.org/10.1016/j.ymgme.2014.04.002
Autor:
Patricia I. Botma, Sandi L. Talbott, Gerald L. Feldman, Jin Fang, Thomas W. Prior, Fatimah A. Nahhas, Thomas J. Monroe, Pamela J. Snyder
Publikováno v:
Genetic Testing and Molecular Biomarkers. 16:187-192
Fragile X syndrome (FXS) is caused by the absence of a functional fragile X mental retardation protein (FMRP). In most cases, the molecular mutation is an expansion and consequent methylation of the CGG trinucleotide repeat in the 5' end of the FMR1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::112288f15696c23b406f57b58ff760bf
https://doi.org/10.1089/gtmb.2011.0128
https://doi.org/10.1089/gtmb.2011.0128
Publikováno v:
American Journal of Medical Genetics Part A. :732-736
We report on a healthy 50-year-old woman who sought predictive testing due to a family history of Huntington disease (HD). Her 73-year-old mother had recently been confirmed to carry an HD allele of 42 CAG repeats, and started to show symptoms of HD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37b8f7709295c15c6fe4deb0c7b3c27e
https://doi.org/10.1002/ajmg.a.32720
https://doi.org/10.1002/ajmg.a.32720
Publikováno v:
American Journal of Medical Genetics Part A. :328-331
We report a 5(1/2)-year-old girl with a maternal family history of Huntington disease (HD), who presented clinically with unbalanced gait, impaired speech, and increasing difficulty with fine motor control. Onset of symptoms began at the age of 3(1/2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd1202b78b36ee3dc34d86e6e4cb516
https://doi.org/10.1002/ajmg.a.30891
https://doi.org/10.1002/ajmg.a.30891
Role for Human SIRT2 NAD-Dependent Deacetylase Activity in Control of Mitotic Exit in the Cell Cycle
Publikováno v:
Molecular and Cellular Biology. 23:3173-3185
Studies of yeast have shown that the SIR2 gene family is involved in chromatin structure, transcriptional silencing, DNA repair, and control of cellular life span. Our functional studies of human SIRT2, a homolog of the product of the yeast SIR2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5930ce927e95d46ac981ed3bdaca7dfa
https://doi.org/10.1128/mcb.23.9.3173-3185.2003
https://doi.org/10.1128/mcb.23.9.3173-3185.2003
Publikováno v:
The Journal of molecular diagnostics : JMD. 16(6)
Triple-primed PCR assays have become the preferred fragile X syndrome testing method. Using a commercially available assay, we detected a reproducible extra peak(s) in 0.5% of 13,161 clinical samples. The objectives of this study were to determine th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8e6c06683aafd63b17f7595d6e5b6215
https://pubmed.ncbi.nlm.nih.gov/25307758
https://pubmed.ncbi.nlm.nih.gov/25307758