Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nicole E Naiman"'
Autor:
David A Davis, Nicole E Naiman, Victoria Wang, Prabha Shrestha, Muzammel Haque, Duosha Hu, Holda A Anagho, Robert F Carey, Katharine S Davidoff, Robert Yarchoan
Publikováno v:
PLoS Pathogens, Vol 11, Iss 7, p e1005064 (2015)
Kaposi's sarcoma-associated herpesvirus (KSHV), also known as human herpesvirus-8, is the causative agent of three hyperproliferative disorders: Kaposi's sarcoma, primary effusion lymphoma (PEL) and multicentric Castleman's disease. During viral late
Externí odkaz:
https://doaj.org/article/d6c410bf28204d7a844e0f158cf3ed42
Autor:
Zak A. Yaffe, Nicole E. Naiman, Jennifer Slyker, Bruce D. Wines, Barbra A. Richardson, P. Mark Hogarth, Rose Bosire, Carey Farquhar, Dorothy Mbori Ngacha, Ruth Nduati, Grace John-Stewart, Julie Overbaugh
Publikováno v:
Cell Reports Medicine, Vol 2, Iss 4, Pp 100254- (2021)
Summary: Defining immune responses that protect humans against diverse HIV strains has been elusive. Studying correlates of protection from mother-to-child transmission provides a benchmark for HIV vaccine protection because passively transferred HIV
Externí odkaz:
https://doaj.org/article/e8da019acae44d7ab5f82c776a75e2a0
Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice
Autor:
Amit K. Srivastava, Samantha R. Renusch, Nicole E. Naiman, Shuping Gu, Amita Sneh, W. David Arnold, Zarife Sahenk, Stephen J. Kolb
Publikováno v:
Neurobiology of Disease, Vol 47, Iss 2, Pp 163-173 (2012)
The small heat shock protein HSPB1 is a multifunctional, α-crystallin-based protein that has been shown to be neuroprotective in animal models of motor neuron disease and peripheral nerve injury. Missense mutations in HSPB1 result in axonal Charcot
Externí odkaz:
https://doaj.org/article/fc27c65b4f7c4ed58e4597788f46a901
Autor:
Nicole E. Naiman, Jennifer Slyker, Barbra A. Richardson, Grace John-Stewart, Ruth Nduati, Julie M. Overbaugh
Publikováno v:
EBioMedicine, Vol 47, Iss, Pp 257-268 (2019)
Background: Antibody-dependent cellular cytotoxicity (ADCC) has been associated with improved infant outcome in mother-to-child transmission (MTCT) of HIV-1. Epitopes of these ADCC-mediating antibodies remain unidentified. CD4-inducible (CD4i) epitop
Publikováno v:
The Journal of Infectious Diseases
Mother-to-child transmission of human immunodeficiency virus (HIV) occurs in the setting of maternal and passively acquired antibodies, providing a unique window into immune correlates of HIV risk. We compared plasma antibody binding to HIV antigens
Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice
Autor:
Nicole E. Naiman, Samantha R. Renusch, Shuping Gu, Zarife Sahenk, W. David Arnold, Stephen J. Kolb, Amit K. Srivastava, Amita Sneh
Publikováno v:
Neurobiology of Disease, Vol 47, Iss 2, Pp 163-173 (2012)
The small heat shock protein HSPB1 is a multifunctional, α-crystallin-based protein that has been shown to be neuroprotective in animal models of motor neuron disease and peripheral nerve injury. Missense mutations in HSPB1 result in axonal Charcot
Autor:
Robert F. Carey, Muzammel Haque, Katharine S. Davidoff, Duosha Hu, Nicole E. Naiman, Prabha Shrestha, David A. Davis, Holda A. Anagho, Robert Yarchoan, Victoria Wang
Publikováno v:
PLoS Pathogens
PLoS Pathogens, Vol 11, Iss 7, p e1005064 (2015)
PLoS Pathogens, Vol 11, Iss 7, p e1005064 (2015)
Kaposi’s sarcoma-associated herpesvirus (KSHV), also known as human herpesvirus-8, is the causative agent of three hyperproliferative disorders: Kaposi’s sarcoma, primary effusion lymphoma (PEL) and multicentric Castleman’s disease. During vira
Autor:
David A. Davis, Sarah I. Daniels, Nicole E. Naiman, Robert Yarchoan, Katharine S. Davidoff, Erin E. Soule
Publikováno v:
Antimicrobial agents and chemotherapy. 56(7)
Inhibitors of HIV protease have proven to be important drugs in combination anti-HIV therapy. These inhibitors were designed to target mature protease and prevent viral particle maturation by blocking Gag and Gag-Pol processing by mature protease. Cu