Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Lina Zelinger"'
Autor:
Lina Zelinger, Charmeine Ko, Francys Alarcon, Samuel Koo, Kenneth Thomas, Hyunjun Nam, Fernando Lopez Diaz, Segun Jung, Fei Ye, Shashikant Kulkarni
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100109- (2023)
Externí odkaz:
https://doaj.org/article/b8d2249ccede4bd8bcf779e33c1c6d7b
Autor:
Samer Khateb, Lina Zelinger, Tamar Ben-Yosef, Saul Merin, Ornit Crystal-Shalit, Menachem Gross, Eyal Banin, Dror Sharon
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51566 (2012)
We used a combined approach of homozygosity mapping and whole exome sequencing (WES) to search for the genetic cause of autosomal recessive retinitis pigmentosa (arRP) in families of Yemenite Jewish origin. Homozygosity mapping of two arRP Yemenite J
Externí odkaz:
https://doaj.org/article/e8b1e0f29bd4411081dfc0412eb8b1ad
Abstract 219: Single-tube NGS profiling allows identification of molecular signature in ALL patients
Autor:
Lina Zelinger, Samuel Koo, Charmeine Ko, Francys Alarcon, Kenneth B. Thomas, Segun C. Jung, Fernando J. Lopez Diaz, Fei Ye, Shashikant Kulkarni
Publikováno v:
Cancer Research. 83:219-219
Background: Acute lymphoblastic leukemia (ALL) can be classified to subtypes by molecular signatures correlating to prognosis and treatment regimen, making accurate molecular profiling of interest for both clinical and research communities. NGS techn
Autor:
Michal Krawczyk, Chaugiang Duong, Lina Zelinger, Fei Ye, Hyunjun Nam, Brad Thomas, Vincent Funari, Shashikant Kulkarni, Fernando Lopez-Diaz
Publikováno v:
Cancer Research. 83:1401-1401
Background: WHO recognizes 23 genomic rearrangements or fusions which define subclasses of AML, MDS/MPN and related neoplasms, and their detection is essential for patient management. Discerning true fusions from artificial calls in RNAseq-based test
Autor:
Lina Zelinger, Tammy M. Martin, Jayshree Advani, Laura Campello, Milton A. English, Alan Kwong, Claire Weber, Jennifer Maykoski, Yuri V. Sergeev, Robert Fariss, Emily Y. Chew, Michael L. Klein, Anand Swaroop
Publikováno v:
iScience. 26:106417
Autor:
Lina Zelinger, Samuel Koo, Francys Alarcon, Charmeine Ko, Brad B Thomas, Segun C Jung, Ying Wang, Fei Ye, Shashikant Kulkarni
Publikováno v:
Blood. 140:11870-11871
Autor:
Lina Zelinger, Anand Swaroop
Publikováno v:
Journal of Clinical Investigation. 130:62-64
Mitochondrial dysfunction or loss is evident in neurodegenerative diseases. Furthermore, mitochondrial DNA (mtDNA) mutations associated with NADH dehydrogenase subunits and nuclear gene mutations that affect mitochondrial function result in optic neu
Autor:
Karen Hendler, Claudia Yahalom, Isabelle Audo, Dror Sharon, Samer Khateb, Alaa AlTalbishi, Christina Zeitz, Prasanthi Namburi, Ruth Sheffer, Eyal Banin, Lina Zelinger
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9, pp.12047. ⟨10.1038/s41598-019-46811-7⟩
Scientific Reports, 2019, 9, pp.12047. ⟨10.1038/s41598-019-46811-7⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-6 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9, pp.12047. ⟨10.1038/s41598-019-46811-7⟩
Scientific Reports, 2019, 9, pp.12047. ⟨10.1038/s41598-019-46811-7⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-6 (2019)
Precise genetic and phenotypic characterization of congenital stationary night blindness (CSNB) patients is needed for future therapeutic interventions. The aim of this study was to estimate the prevalence of CSNB in our populations and to study clin
Autor:
Lina Zelinger, Anand Swaroop
Publikováno v:
Trends in genetics : TIG. 34(5)
For decades, RNA served in a supporting role between the genetic carrier (DNA) and the functional molecules (proteins). Finally, it is time for RNA to take the center stage in all aspects of biology. The retina provides a unique opportunity to dissec
Autor:
Samuel G. Jacobson, Sharon B. Schwartz, Alexander Sumaroka, Susanne Kohl, Alejandro J. Roman, Dror Sharon, Artur V. Cideciyan, Boris Rosin, Bernd Wissinger, Lina Zelinger, Eyal Banin, Anat Blumenfeld, Ada Rosenmann, Cassondra Brown, Dalia Eli, Xunda Luo
Publikováno v:
Ophthalmology. 122:997-1007
Purpose Achromatopsia (ACHM) is a congenital, autosomal recessive retinal disease that manifests cone dysfunction, reduced visual acuity and color vision, nystagmus, and photoaversion. Five genes are known causes of ACHM. The present study took steps