Zobrazeno 1 - 10
of 437
pro vyhledávání: '"Lugar P"'
Assuming the Riemann hypothesis, we prove estimates for the variance of the real and imaginary part of the logarithm of the Riemann zeta-function in short intervals. We give three different formulations of these results. Assuming a conjecture of Chan
Externí odkaz:
http://arxiv.org/abs/2211.14918
Autor:
Zhang Jenny, Grubor Vladimir, Love Cassandra L, Banerjee Anjishnu, Richards Kristy L, Miezcowski Piotr, Dunphy Cherie H, Choi William WL, Auv Wing-Yan, Srivastava Gopesh, Lugar Patricia L, Rizzieri David A, Lagoo Anand S, Bernal-Mizrachi Leon, Mann Karen P, Flowers Christopher R, Naresh Kikkeri N, Evens Andrew M, Gordon Leo I, Czader Magdalena B, Gill Javed I, Hsi Eric D, Liu Qingquan, Fan Alice, Walsh Katherine, Jima Dereje D, Luftig Micah, Ni Ting, Zhu Jun, Chadburn Amy, Levy Shawn, Dunson David B, Dave Sandeep S
Publikováno v:
Infectious Agents and Cancer, Vol 7, Iss Suppl 1, p O1 (2012)
Externí odkaz:
https://doaj.org/article/7638f72d0bc74a6b8be901eec52d3afa
Autor:
Gerson Ascencio, Matthew A de Cruz, Judy Abuel, Sydney Alvarado, Yuma Arriaga, Emily Conrad, Alonso Castro, Katharine Eichelberger, Laura Galvan, Grace Gundy, Jorge Alberto Inojoza Garcia, Alyssa Jimenez, Nhein Tuyet Lu, Catharine Lugar, Ronald Marania, Tserendavaa Mendsaikhan, Jose Ortega, Natasha Nand, Nicole S Rodrigues, Khayla Shabazz, Cynnie Tam, Emmanuel Valenciano, Clive Hayzelden, Anthony S Eritano, Blake Riggs
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 13, Iss 7 (2023)
AbstractThe mechanism surrounding chromosome inheritance during cell division has been well documented, however, organelle inheritance during mitosis is less understood. Recently, the endoplasmic reticulum (ER) has been shown to reorganize during mit
Externí odkaz:
https://doaj.org/article/3d51cddcea8d4c018798a9da598acd29
Autor:
Sarah A. Eisenstein, Raveena S. Boodram, Courtney L. Sutphen, Heather M. Lugar, Brian A. Gordon, Bess A. Marshall, Fumihiko Urano, Anne M. Fagan, Tamara Hershey
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Wolfram syndrome is a rare disease caused by pathogenic variants in the WFS1 gene with progressive neurodegeneration. As an easily accessible biomarker of progression of neurodegeneration has not yet been found, accurate tracking of the neurodegenera
Externí odkaz:
https://doaj.org/article/463b40b8474c45639d3e1a1833e7082c
Autor:
Revista Entre-Lugar
Publikováno v:
Entre-Lugar, Vol 11, Iss 21, Pp 285-292 (2020)
Externí odkaz:
https://doaj.org/article/435ad501c9e74a1586b5ebee97b4c3c2
Autor:
Revista Entre-Lugar
Publikováno v:
Entre-Lugar, Vol 11, Iss 21, Pp 297-309 (2020)
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Externí odkaz:
https://doaj.org/article/a8dd23b805264237adf651a5b81a17e5
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Abstract Background Wolfram syndrome is a rare genetic disease characterized by insulin-dependent diabetes, optic nerve atrophy, sensorineural hearing loss and neurodegeneration. Although olfactory dysfunction, a classical clinical marker of neurodeg
Externí odkaz:
https://doaj.org/article/830f508bfd9c43c98de0c61a75d4b3a4
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Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background Wolfram syndrome is a rare disorder associated with diabetes mellitus, diabetes insipidus, optic nerve atrophy, hearing and vision loss, and neurodegeneration. Sleep complaints are common but have not been studied with objective m
Externí odkaz:
https://doaj.org/article/08e631205e1d4614a133a31d5560ba0b
Autor:
Heather M. Lugar, Jonathan M. Koller, Jerrel Rutlin, Sarah A. Eisenstein, Olga Neyman, Anagha Narayanan, Ling Chen, Joshua S. Shimony, Tamara Hershey
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Abstract Wolfram syndrome is a rare disease caused by mutations in the WFS1 gene leading to symptoms in early to mid-childhood. Brain structural abnormalities are present even in young children, but it is not known when these abnormalities arise. Suc
Externí odkaz:
https://doaj.org/article/41b133a9020c497c8b1dc5bf0c1d1452