Results 121 to 130 of about 104,096 (218)

A Molecularly Defined Medullary Network for Control of Respiratory Homeostasis

open access: yesAdvanced Science, EarlyView.
The dynamic interplay between central respiratory chemoreceptors and the respiratory central pattern generator is essential for maintaining stable respiratory rhythm and patterns, particularly during sleep. This study offers novel insights into the anatomical, molecular, and functional characteristics of a medullary network involving the nucleus ...
Tianjiao Deng   +16 more
wiley   +1 more source

1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 445-458, February 2023., 2023
Abstract Chromosome 1p36 deletion syndrome (1p36DS) is one of the most common terminal deletion syndromes (incidence between 1/5000 and 1/10,000 live births in the American population), due to a heterozygous deletion of part of the short arm of chromosome 1.
Clémence Jacquin   +47 more
wiley   +1 more source

Increasing hourly heavy rainfall in Austria reflected in flood changes. [PDF]

open access: yesNature
Haslinger K   +8 more
europepmc   +1 more source

Enhanced Field‐Like Torque Generated from the Anisotropic Spin‐Split Effect in Triple‐Domain RuO2 for Energy‐Efficient Spin–Orbit Torque Magnetic Random‐Access Memory

open access: yesAdvanced Science, EarlyView.
This study shows an unexplored avenue toward engineering spin‐split effect‐induced spin‐orbit torque (SOT) in triple‐domain structured (100) RuO2/Co‐Fe‐B system where the field‐like torque is significantly enhanced compared with the Slonzewsky‐like torque.
Thi Van Anh Nguyen   +8 more
wiley   +1 more source

Further expansion and confirmation of phenotype in rare loss of YWHAE gene distinct from Miller–Dieker syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 526-539, February 2023., 2023
Abstract Deletion of 17p13.3 has varying degrees of severity on brain development based on precise location and size of the deletion. The most severe phenotype is Miller–Dieker syndrome (MDS) which is characterized by lissencephaly, dysmorphic facial features, growth failure, developmental disability, and often early death.
Elizabeth K. Baker   +9 more
wiley   +1 more source

Leveraging synthetic data to improve regional sea level predictions. [PDF]

open access: yesSci Rep
Tong G   +5 more
europepmc   +1 more source

Deep‐UV Light‐Emitting Based on the hBN:S/hBN: Mg Homojunction

open access: yesAdvanced Science, EarlyView.
S‐atoms are selected as donor dopants to achieve the n‐type conductivity of the hBN film. A theoretical model of S‐doping hBN using DFT calculation and experimentally prepared S‐doped hBN multilayers with a recorded doping concentration of 1.21% is established.
Ransheng Chen   +10 more
wiley   +1 more source

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