Results 161 to 170 of about 791,916 (337)

Non-Syndromic Familial Unerupted Teeth: A Rare Contidion

open access: yesCumhuriyet Dental Journal, 2015
A tooth that remains unerupted beyond the normal time of eruption and fails to erupt is called an impacted tooth. Maxillofacial surgeons encounter the problem of impacted teeth very often.
Akif Türer   +3 more
doaj  

In situ molecular organization and heterogeneity of the Legionella Dot/Icm T4SS

open access: yesFEBS Letters, EarlyView.
We present a nearly complete in situ model of the Legionella Dot/Icm type IV secretion system, revealing its central secretion channel and identifying new components. Using cryo‐electron tomography with AI‐based modeling, our work highlights the structure, variability, and mechanism of this complex nanomachine, advancing understanding of bacterial ...
Przemysław Dutka   +11 more
wiley   +1 more source

Sequence determinants of RNA G‐quadruplex unfolding by Arg‐rich regions

open access: yesFEBS Letters, EarlyView.
We show that Arg‐rich peptides selectively unfold RNA G‐quadruplexes, but not RNA stem‐loops or DNA/RNA duplexes. This length‐dependent activity is inhibited by acidic residues and is conserved among SR and SR‐related proteins (SRSF1, SRSF3, SRSF9, U1‐70K, and U2AF1).
Naiduwadura Ivon Upekala De Silva   +10 more
wiley   +1 more source

Patient-reported disease burden and health care utilization of HAE-nl-C1INH: insights from a real-world survey. [PDF]

open access: yesClin Exp Med
Jones D   +8 more
europepmc   +1 more source

Hereditary Orders [PDF]

open access: yesTransactions of the American Mathematical Society, 1963
openaire   +1 more source

Structural instability impairs function of the UDP‐xylose synthase 1 Ile181Asn variant associated with short‐stature genetic syndrome in humans

open access: yesFEBS Letters, EarlyView.
The Ile181Asn variant of human UDP‐xylose synthase (hUXS1), associated with a short‐stature genetic syndrome, has previously been reported as inactive. Our findings demonstrate that Ile181Asn‐hUXS1 retains catalytic activity similar to the wild‐type but exhibits reduced stability, a looser oligomeric state, and an increased tendency to precipitate ...
Tuo Li   +2 more
wiley   +1 more source

A novel mutation in the transthyretin gene in amyloidosis: A cluster case report in Vietnam

open access: yesVietnam Journal of Science, Technology and Engineering
Transthyretin amyloidosis (ATTR) is a slowly progressive condition characterised by the abnormal accumulation of a protein called amyloid in the body’s organs and tissues.
Ngoc Lan Thi Nguyen   +5 more
doaj  

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