Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Anthony W. Herren"'
Autor:
Katharine Nichole Holm, Anthony W. Herren, Sandra L. Taylor, Jamie L. Randol, Kyoungmi Kim, Glenda Espinal, Verónica Martínez-Cerdeño, Isaac N. Pessah, Randi J. Hagerman, Paul J. Hagerman
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Externí odkaz:
https://doaj.org/article/4c677ac9e0ab44618a1bf3f14f97af69
Autor:
Lisa Ma, Anthony W. Herren, Glenda Espinal, Jamie Randol, Bridget McLaughlin, Veronica Martinez-Cerdeño, Isaac N. Pessah, Randi J. Hagerman, Paul J. Hagerman
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-26 (2019)
Abstract Fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder associated with a premutation repeat expansion (55–200 CGG repeats) in the 5′ noncoding region of the FMR1 gene. Solitary intranuclear inclusions within
Externí odkaz:
https://doaj.org/article/0a0bedd09cce4ced972fc66e7b5aa022
Autor:
Katharine Nichole Holm, Anthony W. Herren, Sandra L. Taylor, Jamie L. Randol, Kyoungmi Kim, Glenda Espinal, Verónica Martínez-Cerdeño, Isaac N. Pessah, Randi J. Hagerman, Paul J. Hagerman
Publikováno v:
Frontiers in Molecular Biosciences, Vol 7 (2021)
Background: Fragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset neurodegenerative disorder associated with premutation CGG-repeat expansions (55–200 repeats) in the 5′ non-coding portion of the fragile X mental retardation 1 (FM
Externí odkaz:
https://doaj.org/article/029f09aa65424d889bdefeeff229c7b7
Autor:
Viju Vijayan Pillai, Luiz G. Siqueira, Moubani Das, Tiffany G. Kei, Lan N. Tu, Anthony W. Herren, Brett S. Phinney, Soon Hon Cheong, Peter J. Hansen, Vimal Selvaraj
Publikováno v:
Biology Open, Vol 8, Iss 5 (2019)
Trophectoderm of blastocysts mediate early events in fetal-maternal communication, enabling implantation and establishment of a functional placenta. Inadequate or impaired developmental events linked to trophoblasts directly impact early embryo survi
Externí odkaz:
https://doaj.org/article/464d89be562f4ecf99afe14f4feda415
Autor:
Stefano Morotti, M. Wallner, Samuel Sossalla, Michael Holzer, Julia Voglhuber, Donald M. Bers, Michael Sacherer, Ingrid Matzer, Stefan Wagner, Natasa Djalinac, Senka Ljubojevic-Holzer, Mahmoud Abdellatif, Simon Sedej, Snjezana Radulovic, Milan Ivanov, Burkert Pieske, Joan Heller Brown, Julie Bossuyt, Brent M. Wood, Anthony W. Herren, Dirk von Lewinski
Publikováno v:
Circulation Research
Rationale: CaMKII (Ca 2+ -Calmodulin dependent protein kinase) δC activation is implicated in pathological progression of heart failure (HF) and CaMKIIδC transgenic mice rapidly develop HF and arrhythmias. However, little is known about early spati
Autor:
James E. Goldman, Alice Tang, Michelle L. Olsen, Natasha L. Pacheco, Jiangtao Li, Daniel Flint, Brett S. Phinney, Anthony W. Herren, Fatima Khan, Michael R. Heaven
Publikováno v:
Molecular & cellular proteomics : MCP, vol 21, iss 1
Molecular & Cellular Proteomics : MCP
Molecular & Cellular Proteomics : MCP
Alexander disease (AxD) is a rare and fatal neurodegenerative disorder caused by mutations in the gene encoding glial fibrillary acidic protein (GFAP). In this report, a mouse model of AxD (GFAPTg;Gfap+/R236H) was analyzed that contains a heterozygou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27db73f1a1ae5cb5705d0a860adbda89
https://hdl.handle.net/10919/111277
https://hdl.handle.net/10919/111277
Autor:
Chad M. Warren, Monika Halas, Paul H. Goldspink, Han-Zhong Feng, Anthony W. Herren, Beata M. Wolska, Pieter P. de Tombe, Jian-Ping Jin, R. John Solaro
Publikováno v:
Molecular and Cellular Biochemistry
Molecular and Cellular Biochemistry, In press, ⟨10.1007/s11010-022-04414-3⟩
Molecular and Cellular Biochemistry, In press, ⟨10.1007/s11010-022-04414-3⟩
International audience; The cardiac isoform of troponin I has a unique N-terminal extension (~ 1-30 amino acids), which contributes to the modulation of cardiac contraction and relaxation. Hearts of various species including humans produce a truncate
Autor:
Brett S. Phinney, Heather E. McKiernan, Kevin M. Legg, Michelle Salemi, Zachary C. Goecker, Glendon J. Parker, Anthony W. Herren
Publikováno v:
Journal of proteome research. 20(10)
Protein is a major component of all biological evidence. Proteomic genotyping is the use of genetically variant peptides that contain single amino acid polymorphisms to infer the genotype of matching non-synonymous single nucleotide polymorphisms for
Publikováno v:
Proteomics. Clinical applicationsREFERENCES. 15(2-3)
Purpose Nonsyndromic craniosynostosis (NCS), the premature fusion of cranial sutures, results in an abnormal skull shape and is associated with a significant morbidity. Proteomics is a promising tool for disease characterization and biomarker discove