Results 21 to 30 of about 3,449 (171)

Perbedaan Ciri Tradisional Sashimi Jepang dan Sashimi di Medan

open access: yes, 2023
This study aims to determine Japanese food restaurants in Medan that provide Sashimi food and the form of difference from sashimi food in downtown Medan with Kyubey Tokyo.
Oktavia, Tri Arta
core  

生食用ホタテガイ貝柱の品質維持および冷蔵中硬化メカニズムに関する研究 [PDF]

open access: yes, 2023
岩手大学博士(農学)原著論文 Niu, Y., Dong, S., Shimakage, N., Wei, H., Yu, K., Yuan, C., & Takaki, K. Differentiation between fresh and frozen‐thawed scallop adductor muscle as raw materials for sashimi during cold storage Journal of Food Science 86(12), 5262-5271 ...
牛, 雅斌, NIU, Yabin
core   +1 more source

Sashimi plots for total RNA time-courses of WT and Δvhs infection.

open access: yes, 2022
For an explanation of sashimi plots see caption to Fig 3. Circular splice junctions are marked in red, linear splice junctions in the same color as read coverage. (PDF)
Adam W. Whisnant (5007887)   +7 more
core   +1 more source

Comparison of sashimi plots generated by ggsashimi and IGV.

open access: yes, 2018
Sashimi plots of 12 ENCODE samples belonging to 3 cell type groups (endothelial, epithelial and mesenchymal) for the region chr10:27040584-27048100 obtained by ggsashimi (A) and the sashimi-plot utility within IGV (B).
Diego Garrido-Martín (5641523)   +3 more
core   +1 more source

Pemanfaatan Iradiasi Gamma pada Ikan Tuna dalam Pembuatan Sushi/Sashimi [PDF]

open access: yes, 2018
Sushi/sashimi merupakan makanan yang berisiko tinggi menyebabkan foodborne disease. Teknik suhu tinggi tidak dapat diterapkan pada makanan ini karena menyebabkan perubahan tekstur yang signifikan.
Kiyat, Warsono El   +2 more
core   +2 more sources

SASHIMI-SIDM: semi-analytical subhalo modelling for self-interacting dark matter at sub-galactic scales [PDF]

open access: yes
: We combine the semi-analytical structure formation model, SASHIMI, which predicts subhalo populations in collisionless, cold dark matter (CDM), with a parametric model that maps CDM halos to self-interacting dark matter (SIDM) halos ...
Horigome, Shunichi   +4 more
core   +1 more source

Sashimi plots for mock, WT-F and ΔICP22 infection at 8 h p.i.

open access: yes, 2022
For an explanation of sashimi plots see caption to Fig 3. Circular splice junctions are marked in red, linear splice junctions in the same color as read coverage. (PDF)
Adam W. Whisnant (5007887)   +7 more
core   +1 more source

Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4

open access: yesMovement Disorders, EarlyView.
Abstract Background SRRM4 is an exclusively neural‐expressed splicing‐factor gene not yet associated with a monogenic condition. Objective We sought to delineate movement disorders caused by SRRM4 variants. De novo splice‐donor‐site variants at position +2 of intron 5 of SRRM4 (c.464+2T>C, c.464+2T>A) occurred in three unrelated patients with dystonia ...
Philip Harrer   +24 more
wiley   +1 more source

The state of knowledge on four families of Syngnathoidei fishes (Teleostei: Syngnathiformes): Aulostomidae, Centriscidae, Fistulariidae and Solenostomidae

open access: yesJournal of Fish Biology, EarlyView.
Abstract Knowledge on the ecology and life‐history traits of coastal marine species is vital to inform their conservation and management, especially as their coastal habitats come under increasing threats. However, such data have never been collated for four of the five families in the suborder Syngnathoidei—the close relatives of the better‐studied ...
Syd J. Ascione   +3 more
wiley   +1 more source

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1719-1724, July 2026.
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi   +11 more
wiley   +1 more source

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