Zobrazeno 1 - 10
of 18
pro vyhledávání: '"M. K. Farhan"'
Publikováno v:
The Iraqi Journal of Agricultural science, Vol 54, Iss 2 (2023)
Using the policy of price has a significant impact to developing the production of a particular crop by increasing productivity, which is eventually reflected in achieving high rates of self-sufficiency of the crops. The research objective is to iden
Externí odkaz:
https://doaj.org/article/8a1878baafcc4564a1f59f0f06214e66
Autor:
Allison A. Dilliott, Abdalla Abdelhady, Kelly M. Sunderland, Sali M. K. Farhan, Agessandro Abrahao, Malcolm A. Binns, Sandra E. Black, Michael Borrie, Leanne K. Casaubon, Dar Dowlatshahi, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, Morris Freedman, David Grimes, Ayman Hassan, Mandar Jog, Sanjeev Kumar, Donna Kwan, Anthony E. Lang, Jennifer Mandzia, Mario Masellis, Adam D. McIntyre, Stephen H. Pasternak, Bruce G. Pollock, Tarek K. Rajji, Ekaterina Rogaeva, Demetrios J. Sahlas, Gustavo Saposnik, Christine Sato, Dallas Seitz, Christen Shoesmith, Thomas D. L. Steeves, Richard H. Swartz, Brian Tan, David F. Tang-Wai, Maria C. Tartaglia, John Turnbull, Lorne Zinman, ONDRI Investigators, Robert A. Hegele
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
Abstract Genetic factors contribute to neurodegenerative diseases, with high heritability estimates across diagnoses; however, a large portion of the genetic influence remains poorly understood. Many previous studies have attempted to fill the gaps b
Externí odkaz:
https://doaj.org/article/c14898e55b0f4ab5b45663002d305766
Autor:
Rossella Spataro, Maria Kousi, Sali M. K. Farhan, Jason R. Willer, Jay P. Ross, Patrick A. Dion, Guy A. Rouleau, Mark J. Daly, Benjamin M. Neale, Vincenzo La Bella, Nicholas Katsanis
Publikováno v:
Human Genomics, Vol 13, Iss 1, Pp 1-10 (2019)
Abstract Background Amyotrophic lateral sclerosis [1] is a genetically heterogeneous neurodegenerative disorder, characterized by late-onset degeneration of motor neurons leading to progressive limb and bulbar weakness, as well as of the respiratory
Externí odkaz:
https://doaj.org/article/2ca1793b76fd4a3483f28594050062e2
Publikováno v:
IRAQI JOURNAL OF AGRICULTURAL SCIENCES. 54:609-618
Using the policy of price has a significant impact to developing the production of a particular crop by increasing productivity, which is eventually reflected in achieving high rates of self-sufficiency of the crops. The research objective is to iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cebbfad993909fa9ac74227050bd48cf
https://doi.org/10.36103/ijas.v54i2.1737
https://doi.org/10.36103/ijas.v54i2.1737
Autor:
Sali M. K. Farhan, Jian Wang, John F. Robinson, Piya Lahiry, Victoria M. Siu, Chitra Prasad, Jonathan B. Kronick, David A. Ramsay, C. Anthony Rupar, Robert A. Hegele
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 1, Pp 73-80 (2014)
Abstract Iron‐sulfur (Fe‐S) clusters are a class of highly conserved and ubiquitous prosthetic groups with unique chemical properties that allow the proteins that contain them, Fe‐S proteins, to assist in various key biochemical pathways. Mutat
Externí odkaz:
https://doaj.org/article/1eb51256fe8f4b6ca24045e47c3b068a
Autor:
Jay P. Ross, Fulya Akcimen, Calwing Liao, Dan Spiegelman, Ben Weisburd, Nicolas Dupré, Patrick A. Dion, Guy A. Rouleau, Sali M. K. Farhan
Lowered expression of STMN2 is associated with TDP-43 pathology in amyotrophic lateral sclerosis (ALS). Recently, the number of dinucleotide CA repeats in an intron of the STMN2 gene was reported to be associated with increased risk for ALS. Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2dd993fbcbf659b85bbf39db7aa0bed
https://doi.org/10.1101/2022.04.30.22273566
https://doi.org/10.1101/2022.04.30.22273566
Autor:
Jay P, Ross, Fulya, Akçimen, Calwing, Liao, Dan, Spiegelman, Ben, Weisburd, Nicolas, Dupré, Patrick A, Dion, Guy A, Rouleau, Sali M K, Farhan
Publikováno v:
Neurology. Genetics. 8(4)
Recently, the number of dinucleotide CA repeats in an intron of theHere, we used whole-genome sequencing and tested theWe find that repeats well above the previously reported pathogenic threshold of 19 are commonly observed in unaffected individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3585d295be8658dc0b3cc58b4a82b3e5
https://pubmed.ncbi.nlm.nih.gov/35923349
https://pubmed.ncbi.nlm.nih.gov/35923349
Autor:
Ekaterina Rogaeva, Leanne K. Casaubon, David F. Tang-Wai, Corinne E. Fischer, Michael Borrie, Morris Freedman, Christen Shoesmith, Donna Kwan, Elizabeth Finger, Brian Tan, Maria Carmela Tartaglia, Gustavo Saposnik, Sanjeev Kumar, Malcolm A. Binns, Dallas Seitz, Sandra E. Black, Mandar Jog, Richard H. Swartz, Sali M K Farhan, John Turnbull, Andrew Frank, Abdalla Abdelhady, Bruce G. Pollock, Kelly M Sunderland, Robert A. Hegele, David Grimes, Agessandro Abrahao, Stephen H. Pasternak, Thomas Steeves, Demetrios J. Sahlas, Dar Dowlatshahi, Christine Sato, Ayman Hassan, Anthony E. Lang, Lorne Zinman, Ondri Investigators, Mario Masellis, Adam D. McIntyre, Allison A Dilliott, Tarek K. Rajji, Jennifer Mandzia
Publikováno v:
NPJ Genomic Medicine
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
Genetic factors contribute to neurodegenerative diseases, with high heritability estimates across diagnoses; however, a large portion of the genetic influence remains poorly understood. Many previous studies have attempted to fill the gaps by perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2cb199ee23b0bbf2488d4744c489aeb
https://doi.org/10.1038/s41525-021-00243-3
https://doi.org/10.1038/s41525-021-00243-3
Autor:
Patrick M. Dooley, Bradley T. Hyman, Pia Kivisäkk, James D. Berry, Teresa Gomez-Isla, Tiziana Petrozziello, Steven E. Arnold, Ghazaleh Sadri-Vakili, Bianca A. Trombetta, Ana C. Amaral, James Chan, Tara L. Spires-Jones, Alexandra N. Mills, Derek H. Oakley, Anubrata Ghosal, Caitlin Commins, Merit Cudkowicz, Simon Dujardin, Sali M K Farhan, Theresa R Connors, Evan A. Bordt, Spencer E. Kim
Publikováno v:
Brain pathology (Zurich, Switzerland). 32(2)
Although the molecular mechanisms underlying amyotrophic lateral sclerosis (ALS) are not yet fully understood, several studies report alterations in tau phosphorylation in both sporadic and familial ALS. Recently, we have demonstrated that phosphoryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1213b8764c788efc75c47803b3709591
https://pubmed.ncbi.nlm.nih.gov/34779076
https://pubmed.ncbi.nlm.nih.gov/34779076
Autor:
Allison A. Dilliott, Catherine M. Andary, Meaghan Stoltz, Andrey A. Petropavlovskiy, Sali M. K. Farhan, Martin L. Duennwald
Publikováno v:
International Journal of Molecular Sciences. 23:4076
Protein misfolding is a common basis of many neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). Misfolded proteins, such as TDP-43, FUS, Matrin3, and SOD1, mislocalize and form the hallmark cytoplasmic and nuclear inclusions in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47393ad78cc4fabbfb248c316a01de42
https://doi.org/10.3390/ijms23084076
https://doi.org/10.3390/ijms23084076