Results 61 to 70 of about 1,174,028 (302)

Diversity and complexity in neural organoids

FEBS Letters, EarlyView.
Neural organoid research aims to expand genetic diversity on one side and increase tissue complexity on the other. Chimeroids integrate multiple donor genomes within single organoids. Self‐organising multi‐identity organoids, exogenous cell seeding, or enforced assembly of region‐specific organoids contribute to tissue complexity.
Ilaria Chiaradia, Madeline A. Lancaster
wiley   +1 more source

Identification of Deletion and Duplication Genotypes of the Pmp22 Gene Using Pcr-Rflp, Competitive Multiplex Pcr, and Multiplex Ligation- Dependent Probe Amplification: A Comparison

, 2009
We evaluated the efficacy of PCR-RFLP, competitive multiplex PCR, and a commercially available system of multiplex ligation-dependent probe amplification (MLPA) for the determination of deletion and duplication genotypes of the PMP22 gene.
HUNG, CHIA-CHENG;LEE, CHIEN-NAN;LIN, CHIA-YUN;CHENG, WEN-FANG;CHEN, CHI-AN;HSIEH, SUNG-TSANG;YANG, CHIH-CHAO;JONG, YUH- JYH;SU, YI-NING;LIN, WIN-LI, 洪加政;李建南;林佳儀;鄭文芳;陳祈安;謝松蒼;楊智超;鐘育志;蘇怡寧;林文澧   +1 more
core   +1 more source

Dominant-Negative Proteins in Herpesviruses – From Assigning Gene Function to Intracellular Immunization

Viruses, 2009
Investigating and assigning gene functions of herpesviruses is a process, which profits from consistent technical innovation. Cloning of bacterial artificial chromosomes encoding herpesvirus genomes permits nearly unlimited possibilities in the ...
Zsolt Ruzsics, Ulrich H. Koszinowski, Hermine Mühlbach, Christian A. Mohr   +3 more
doaj   +1 more source

Cryptography with Certified Deletion

, 2023
We propose a new, unifying framework that yields an array of cryptographic primitives with certified deletion. These primitives enable a party in possession of a quantum ciphertext to generate a classical certificate that the encrypted plaintext has been information-theoretically deleted, and cannot be recovered even given unbounded computational ...
James Bartusek, Dakshita Khurana
openaire   +4 more sources

Septin 9 PB domains coordinate centrosome positioning and microtubule acetylation to control epithelial polarity

FEBS Letters, EarlyView.
Septin 9 polybasic domains couple phosphoinositide‐rich membrane binding to centrosome positioning, Golgi organization, and microtubule acetylation to control epithelial polarity. Their loss disrupts this axis, causing centrosome mispositioning, Golgi fragmentation, reduced microtubule acetylation, and polarity inversion via upregulation of the ...
Ting ting Cai, Mohyeddine Omrane, Nassima Benzoubir, Didier Samuel, Ama Gassama‐Diagne   +4 more
wiley   +1 more source

Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-CardioFacial syndrome) [PDF]

, 2005
Deletion 22q11.2 syndrome (Del22) (DiGeorge/Velo-Cardio-Facial syndrome) is characterized by congenital heart defect (CHD), palatal anomalies, facial dysmorphisms, neonatal hypocalcemia, immune deficit, speech and learning disabilities. CHD is present
Marino, Bonnie, Capolino, Rossella, Digilio, Maria Cristina, Dallapiccola, B.   +3 more
core  

Deletion- type DVGs identified in viruses #1 and #2 using DVG-profiler.

, 2019
Deletion- type DVGs identified in viruses #1 and #2 using DVG-profiler.
Majid Laassri (4976732), Svetlana Petrovskaya (799917), Trent J. Bosma (6710897), Konstantinos Karagiannis (191147), Natalia Ilyushina (5194505), Steven Rubin (1877446), Tatiana Zagorodnyaya (799916), Vahan Simonyan (57547), Luis Santana-Quintero (576164), Christian J. Sauder (6710900), Raymond P. Donnelly (317850)   +10 more
core   +1 more source

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMAworking groups on CNVs [PDF]

, 2022
The Enhancing NeuroImaging Genetics through Meta‐Analysis copy number variant (ENIGMA‐CNV) and 22q11.2 Deletion Syndrome Working Groups (22q‐ENIGMA WGs) were created to gain insight into the involvement of genetic factors in human brain development and ...
Ge, T., Boomsma, D., Grabe, H., Jalbrzikowski, M., McDonald-McGinn, D., Hashimoto, R., Holmes, A., Vassos, E., Stefánsson, K., Martínez, K., Mathias, S., Paus, T., Rodriguez‐Herreros, B., Draganski, B. ; https://orcid.org/, Van der Meer, D., Liu, J., Craig, M., Hottenga, J., Amunts, K., Ayesa‐Arriola, R., Hansen, L., Armstrong, N., Chow, E., Vila‐Rodriguez, F., Westlye, L., van Ent, D., Bassett, A., Espeseth, T., Glahn, D., Vila-Rodriguez, F., Reis Marques, T., Jacquemont, S., Monereo Sánchez, J., Arango, C., Prieto, C., Ching, C., Roalf, D., Draganski, B., Calhoun, V., Rucker, J., Moreau, C., Wittfeld, K., Mather, K., Gutman, B., Cichon, S., Ulfarsson, M., Tamnes, C., Thompson, P., Reymond, A., Crespo‐Facorro, B., Djurovic, S., Repetto, G., Walters, G., Vajdi, A., Sun, D., Haavik, J., Pol, H., Gur, R., Rodriguez-Herreros, B., Vázquez-Bourgon, J., Sánchez, J., Crespo-Facorro, B., Stefansson, H., Agartz, I., McDonald‐McGinn, D., Bearden, C., Donohoe, G., Sønderby, I., Hulshoff Pol, H., Ehrlich, S., Kushan, L., Thomopoulos, S., Cunningham, A., Silva, A., McRae, A., Modenato, C., Moberget, T., Butcher, N., Martin‐Brevet, S., Zackai, E., Lundervold, A., Marques, T., Van den Bree, M., Dale, A., Hibar, D., Martin-Brevet, S., Mühleisen, T., Schmitt, J., Villalon‐Reina, J., Vázquez‐Bourgon, J., Medland, S., Ciufolini, S., Knowles, E., Pausova, Z., Bakker, G., Villalon-Reina, J., Linden, D., Wen, W., Bülow, R., Doherty, J., Emanuel, B., Van 't Ent, D., Stein, D., Tordesillas-Gutiérrez, D., Fisher, S., Andreassen, O., Håberg, A., Ragothaman, A., Reinbold, C., Tordesillas‐Gutiérrez, D., Caspers, S., De Zubicaray, G., Ayesa-Arriola, R., Schofield, P., Sachdev, P., Durdle, C., Dazzan, P.   +116 more
core   +1 more source

VERBAL GAPPING IN SERBIAN

Filolog, 2021
This paper explores the syntactic structure of verbal gapping in Serbian in the framework of the generative theoretical approach and the ways in which this type of ellipsis differs in Serbian and English.
Lazar S. Savković
doaj  

Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR

Hematology, 2022
Background The α-thalassemia is a highly prevalent disease in tropical and subtropical regions, including southern China, and is mainly caused by deletion in α-globin genes (HBA1 and HBA2). The clinical manifestation of α-thalassemia is highly correlated
Xiuqin Bao, Danqing Qin, Jian Ma, Xiangcheng Zhou, Jicheng Wang, Cuize Yao, Liang Zhang, Li Du   +7 more
doaj   +1 more source