Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hengameh Zahed"'
Autor:
Hengameh Zahed, Timothy J. Denison, José Rafael P. Zuzuárregui, Roee Gilron, Philip A. Starr, Simon Little
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 36(7)
Sleep disturbances are among the most common nonmotor complications of Parkinson's disease (PD), can present in prodromal stages, and progress with advancing disease. In addition to being a symptom of neurodegeneration, sleep disturbances may also co
Publikováno v:
Molecular Genetics & Genomic Medicine
Background When a family encounters the loss of a child early in life, extensive genetic testing of the affected neonate is sometimes not performed or not possible. However, the increasing availability of genomic sequencing may allow for direct appli
Autor:
Sarah L. Patterson, R. Krishna Chaganti, Kashif Jafri, Katherine D Wysham, Amber Nolan, Matthew D. Bucknor, Hengameh Zahed
Publikováno v:
Clinical rheumatology. 36(6)
Weakness, seizures, and encephalopathy have a broad differential diagnosis in patients with systemic lupus erythematosus (SLE). We present a case of a 26-year-old female with a recent diagnosis of SLE who experienced a clinical deterioration with qua
Publikováno v:
Radiation Research. 170:353-364
To determine whether the physical differences between high- and low-LET radiation are reflected in the biological responses of exposed cells, we detailed phospho-protein profiles of three proteins functional in radiation repair and signal transductio
Publikováno v:
The Journal of Pediatrics. 189:222-226.e1
We present cases of 3 children diagnosed with the same genetic condition, Gitelman syndrome, at different stages using various genetic methods: panel testing, targeted single gene sequencing, and exome sequencing. We discuss the advantages and disadv
Autor:
Joan S. Steffan, Kurt F. Weiberth, Aaron C. Daub, Alexander P. Osmand, Hengameh Zahed, Alice Lau, Ian H. Kratter, Steven Finkbeiner, Xiaofeng Gu, X. William Yang, Eliezer Masliah, Andrey S. Tsvetkov, Sandrine Humbert, Frédéric Saudou
Publikováno v:
The Journal of clinical investigation. 126(9)
Huntington's disease (HD) is a progressive, adult-onset neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the N-terminal region of the protein huntingtin (HTT). There are no cures or disease-modifying therapies for HD. HTT has
Autor:
Hengameh Zahed, Wei Chun Chang, Trieu Nguyen, Edward C. Hsiao, Jennifer K. Ng, Mark J. Scott, Bruce R. Conklin
Publikováno v:
Stem Cell Research & Therapy
Hsiao, Edward C; Nguyen, Trieu D; Ng, Jennifer K; Scott, Mark J; Chang, Wei Chun; Zahed, Hengameh; et al.(2011). Constitutive Gs activation using a single-construct tetracycline-inducible expression system in embryonic stem cells and mice. Stem Cell Research & Therapy, 2(2), 11. doi: http://dx.doi.org/10.1186/scrt52. Retrieved from: http://www.escholarship.org/uc/item/6762x12t
Hsiao, Edward C; Nguyen, Trieu D; Ng, Jennifer K; Scott, Mark J; Chang, Wei Chun; Zahed, Hengameh; et al.(2011). Constitutive Gs activation using a single-construct tetracycline-inducible expression system in embryonic stem cells and mice. Stem Cell Research & Therapy, 2(2), 11. doi: http://dx.doi.org/10.1186/scrt52. Retrieved from: http://www.escholarship.org/uc/item/6762x12t
Introduction The controlled expression of many genes, including G-protein coupled receptors (GPCRs), is important for delineating gene functions in complex model systems. Binary systems for inducible regulation of transgene expression are widely used