User profiles for Dinesh Soares
Dinesh SoaresAmerican Society for Microbiology (formerly American Chemical Society / University of … Verified email at asmusa.org Cited by 4282 |
[PDF][PDF] SAF-A regulates interphase chromosome structure through oligomerization with chromatin-associated RNAs
RS Nozawa, L Boteva, DC Soares, C Naughton… - Cell, 2017 - cell.com
Higher eukaryotic chromosomes are organized into topologically constrained functional
domains; however, the molecular mechanisms required to sustain these complex interphase …
domains; however, the molecular mechanisms required to sustain these complex interphase …
[HTML][HTML] A structurally distinct TGF-β mimic from an intestinal helminth parasite potently induces regulatory T cells
Helminth parasites defy immune exclusion through sophisticated evasion mechanisms,
including activation of host immunosuppressive regulatory T (Treg) cells. The mouse parasite …
including activation of host immunosuppressive regulatory T (Treg) cells. The mouse parasite …
[PDF][PDF] HpARI protein secreted by a helminth parasite suppresses interleukin-33
Infection by helminth parasites is associated with amelioration of allergic reactivity, but
mechanistic insights into this association are lacking. Products secreted by the mouse parasite …
mechanistic insights into this association are lacking. Products secreted by the mouse parasite …
DISC1: structure, function, and therapeutic potential for major mental illness
Disrupted in schizophrenia 1 (DISC1) is well established as a genetic risk factor across a
spectrum of psychiatric disorders, a role supported by a growing body of biological studies, …
spectrum of psychiatric disorders, a role supported by a growing body of biological studies, …
[PDF][PDF] A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression
…, BS Pickard, A Maclean, MP Malloy, DC Soares… - The American Journal of …, 2009 - cell.com
Schizophrenia and bipolar disorder are leading causes of morbidity across all populations,
with heritability estimates of ∼80% indicating a substantial genetic component. Population …
with heritability estimates of ∼80% indicating a substantial genetic component. Population …
[HTML][HTML] RPGR: Its role in photoreceptor physiology, human disease, and future therapies
RD Megaw, DC Soares, AF Wright - Experimental eye research, 2015 - Elsevier
Mammalian photoreceptors contain specialised connecting cilia that connect the inner (IS)
to the outer segments (OS). Dysfunction of the connecting cilia due to mutations in ciliary …
to the outer segments (OS). Dysfunction of the connecting cilia due to mutations in ciliary …
DISC1 genetics, biology and psychiatric illness
…, ELV Malavasi, E Grünewald, DC Soares… - Frontiers in biology, 2013 - Springer
Psychiatric disorders are highly heritable, and in many individuals likely arise from the
combined effects of genes and the environment. A substantial body of evidence points toward …
combined effects of genes and the environment. A substantial body of evidence points toward …
DISC1 complexes with TRAK1 and Miro1 to modulate anterograde axonal mitochondrial trafficking
…, JE Eykelenboom, DC Soares… - Human molecular …, 2014 - academic.oup.com
Disrupted-In-Schizophrenia 1 (DISC1) is a candidate risk factor for schizophrenia, bipolar
disorder and severe recurrent depression. Here, we demonstrate that DISC1 associates …
disorder and severe recurrent depression. Here, we demonstrate that DISC1 associates …
[HTML][HTML] Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations
We identified four different missense mutations in the single-exon gene MAB21L2 in eight
individuals with bilateral eye malformations from five unrelated families via three independent …
individuals with bilateral eye malformations from five unrelated families via three independent …
[HTML][HTML] Structural models of human eEF1A1 and eEF1A2 reveal two distinct surface clusters of sequence variation and potential differences in phosphorylation
Background Despite sharing 92% sequence identity, paralogous human translation elongation
factor 1 alpha-1 (eEF1A1) and elongation factor 1 alpha-2 (eEF1A2) have different but …
factor 1 alpha-1 (eEF1A1) and elongation factor 1 alpha-2 (eEF1A2) have different but …