Results 231 to 240 of about 256,625 (325)

Tau‐targeting active immunotherapy slows progression and reduces pathology in mouse models of tauopathy

open access: yesBrain Pathology, EarlyView.
The efficacy of the novel anti‐tau active immunotherapy, p5555kb, was tested using two mouse models of tau pathology. p5555kb inoculation increased the survival rate and reduced tau pathology in tau‐overexpressing P301L mice and decreased tau seeding in the brains of C57BL/6 mice injected with human‐purified Alzheimer's disease tau.
Christopher M. Brown   +7 more
wiley   +1 more source

ADIPOQ polymorphisms and haplotypes affect circulating adiponectin levels and their association with gestational hypertension and preeclampsia. [PDF]

open access: yesFront Physiol
Fróes de Castro RN   +8 more
europepmc   +1 more source

Haplotype-resolved assembly of diploid and polyploid genomes using quantum computing [PDF]

open access: gold
Yibo Chen   +5 more
openalex   +1 more source

Median-joining network for PpSP29 <i>P</i>. <i>papatasi</i> haplotypes.

open access: green, 2020
Catherine M. Flanley   +13 more
openalex   +2 more sources

A century of theories of balancing selection

open access: yesBiological Reviews, EarlyView.
ABSTRACT Traits that affect organismal fitness are often highly genetically variable. This genetic variation is vital for populations to adapt to their environments, but it is also surprising given that nature – after all – ‘selects’ the best genotypes at the expense of those that fall short.
Filip Ruzicka   +10 more
wiley   +1 more source

Genetic diversity and geographic distribution of Fasciola species from cattle in eight provinces of South Africa. [PDF]

open access: yesSci Rep
Nukeri S   +6 more
europepmc   +1 more source

Haplotyp [PDF]

open access: yes, 2018
openaire   +1 more source

Fetal Fraction Signatures: A Quality Control Tool to Detect Potentially Confounding Situations in NonInvasive Prenatal Diagnosis of Monogenic Conditions

open access: yesClinical Genetics, EarlyView.
Noninvasive prenatal diagnosis for monogenic diseases (NIPD‐M) to detect inherited mutations is performed in parallel with fetal fraction signatures, to detect various anomalies that may compromise diagnosis. An extra regression analysis may be necessary to resolve mosaic situations. ABSTRACT Noninvasive prenatal diagnosis relies on the analysis of the
Jean‐Louis Blouin   +2 more
wiley   +1 more source

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