keyword
https://read.qxmd.com/read/38389734/comparative-evaluation-of-remineralization-potential-of-four-different-remineralization-agents-on-human-enamel-an-in-vitro-study
#21
JOURNAL ARTICLE
Giftlin Denny Xavier, George Thomas, Sunil Jose, V J Vivek, Kanimozhi Selvam, Ashish Ramakrishnan
AIM: The study aimed to assess the remineralizing potential of four different commercially available agents using a Scanning Electron Microscope (SEM), energy dispersive X-ray (EDX) analysis, and Vickers Microhardness (VMH) Test. MATERIALS AND METHODS: Forty-four specimens ( n = 11 per group) were prepared from extracted teeth. A window of 6 mm × 4 mm was made on all the specimens that represented three zones, namely, sound enamel, demineralized enamel, and remineralized enamel...
January 2024: J Conserv Dent Endod
https://read.qxmd.com/read/38388987/the-effect-of-nano-silver-fluoride-self-assembling-peptide-and-sodium-fluoride-varnish-on-salivary-cariogenic-bacteria-a-randomized-controlled-clinical-trial
#22
RANDOMIZED CONTROLLED TRIAL
Sara M Atteya, Hala A Amer, Susan M Saleh, Yara Safwat
OBJECTIVES: To compare the antibacterial effect of Nanosilver Fluoride varnish (NSF) varnish, P11-4 and Sodium Fluoride (NaF) varnish against salivary Streptococcus mutans (S. mutans) and Lactobacilli. METHODS: 66 patients aged 10-24 years old were randomly assigned to receive single application of NSF, P11-4 or NaF varnish. Baseline unstimulated saliva samples were collected before the agents were applied and S.mutans and Lactobacilli colony forming units (CFU) were counted...
February 23, 2024: Clinical Oral Investigations
https://read.qxmd.com/read/38357262/prenatal-diagnosis-of-a-de-novo-2q14-3-q22-1-deletion-with-complex-chromosomal-rearrangement
#23
JOURNAL ARTICLE
Yong Wu, Chuanning Liao, Yamei Xie, Lingxi Wang
INTRODUCTION: Chromosomal aberrations due to complex chromosomal rearrangements (CCRs) can cause abnormal phenotypes if accompanied by microdeletions or microduplications near the breakpoint, or gene breaks. CASE PRESENTATION: We report a prenatal diagnostic case of 2q14.3-q22.1 deletion with ultrasound suggestive of absent nasal bone accompanied by CCRs involving 6 chromosomes. Cytogenetic analysis revealed a karyotype of 46,XY,der(1)t(1;2)(p13.3;p11.2),der(2)t(1;2)inv(2)(q12q14...
February 2024: Molecular Syndromology
https://read.qxmd.com/read/38347522/novel-kmt2b-gene-mutation-in-muc4-positive-low-grade-fibromyxoid-sarcoma
#24
JOURNAL ARTICLE
Liying Zhang, Luqiao Luo, Chao Liu, Zhi Li
BACKGROUND: Low-grade Fibromyxoid Sarcoma(LGFM)is a rare fibrosarcoma, which mainly occurs in young people and is mostly seen in the trunk and limbs. The tumor is usually FUS-CREB3L2 fusion caused by t(7;16)(q32-34;p11)chromosome translocation, and rarely FUS-CREB3L1 and EWSR1-CREB3L1 fusion. MUC4 diffuse strong positive can be used as a specific index of LGFM. LGFM is similar to Sclerosing Epithelioid Fibrosarcoma(SEF) and may have the same origin. CASE PRESENTATION: We report a case of LGFM in the chest wall...
February 12, 2024: Diagnostic Pathology
https://read.qxmd.com/read/38310082/recent-progress-in-understanding-the-intracellular-domain-s-gating-and-functional-roles-in-trimeric-ligand-gated-ion-channels
#25
JOURNAL ARTICLE
Yan Lu, Yi Yu Lin, Jin Wang
Ligand-gated ion channels are a large category of essential ion channels, whose superfamily members may modulate their state by binding to specific ligands, allowing specific ions to pass through the cell membrane. Purinergic ligand- gated ion channel(P2X)and ASIC (acid-sensitive ion channel) are representative members of trimeric ligand-gated ion channels. Recent studies have shown that structural differences in the intracellular domain of P2X receptors (P2XR) may determine the desensitization process. The lateral fenestrations of P2XR potentially serve as a pathway for ion conduction and play a decisive role in ion selectivity...
February 2, 2024: Zhejiang da Xue Xue Bao. Yi Xue Ban, Journal of Zhejiang University. Medical Sciences
https://read.qxmd.com/read/38254992/non-invasive-prenatal-test-analysis-opens-a-pandora-s-box-identification-of-very-rare-cases-of-sry-positive-healthy-females-segregating-for-three-generations-thanks-to-preferential-inactivation-of-the-xqyp-translocated-chromosome
#26
Cristina Politi, Katia Grillone, Donatella Nocera, Emma Colao, Michelle Li Bellisario, Sara Loddo, Giorgia Catino, Antonio Novelli, Nicola Perrotti, Iuliano Rodolfo, Paola Malatesta
The translocation of the testis-determining factor, the SRY gene, from the Y to the X chromosome is a rare event that causes abnormalities in gonadal development. In all cases of males and females carrying this translocation, disorder of sex development is reported. In our study, we described a peculiar pedigree with the first evidence of four healthy females from three generations who are carriers of the newly identified t(X;Y)(q28;p11.2)(SRY+) translocation with no evidence of ambiguous genitalia or other SRY-dependent alterations...
January 16, 2024: Genes
https://read.qxmd.com/read/38237357/genetic-recombination-and-genotype-diversity-of-norovirus-gi-in-children-with-acute-gastroenteritis-in-thailand-2015-2021
#27
JOURNAL ARTICLE
Pattara Khamrin, Kattareeya Kumthip, Arpaporn Yodmeeklin, Shoko Okitsu, Kazushi Motomura, Shintaro Sato, Hiroshi Ushijima, Niwat Maneekarn
BACKGROUND: Human norovirus is a predominant etiological agent responsible for acute gastroenteritis across all age groups. Recently, norovirus recombinant strains have been reported as the cause of norovirus outbreaks in several settings and the strains that cause outbreaks mostly belong to the norovirus GII. However, yet, the norovirus GI recombinant strains have never been reported previously in Thailand. The aims of this study were to investigate the genetic recombination and genotype diversity of norovirus GI strains in children hospitalized with acute gastroenteritis in Chiang Mai, Thailand during a period of seven years from 2015 to 2021...
January 12, 2024: Journal of Infection and Public Health
https://read.qxmd.com/read/38235171/intranasal-insulin-attenuates-hypoxia-ischemia-induced-short-term-sensorimotor-behavioral-disturbances-neuronal-apoptosis-and-brain-damage-in-neonatal-rats
#28
JOURNAL ARTICLE
Chirag P Talati, Jonathan W Lee, Silu Lu, Norma B Ojeda, Varsha Prakash, Nilesh Dankhara, Tanner C Nielson, Sara P Sandifer, Gene L Bidwell, Yi Pang, Lir-Wan Fan, Abhay J Bhatt
There is a significant need for additional therapy to improve outcomes for newborns with acute Hypoxic-ischemic (HI) encephalopathy (HIE). New evidence suggests that insulin could be neuroprotective. This study aimed to investigate whether intranasal insulin attenuates HI-induced brain damage and neurobehavioral dysfunction in neonatal rats. Postnatal day 10 (P10), Sprague-Dawley rat pups were randomly divided into Sham + Vehicle, Sham + Insulin, HI + Vehicle, and HI + Insulin groups with equal male-to-female ratios...
2024: Current research in neurobiology
https://read.qxmd.com/read/38216246/detection-of-45-x-46-x-r-x-p11-3q22-1-in-a-17-year-old-girl-with-secondary-amenorrhea-short-stature-and-normal-intelligence
#29
JOURNAL ARTICLE
Chih-Ping Chen
No abstract text is available yet for this article.
January 2024: Taiwanese Journal of Obstetrics & Gynecology
https://read.qxmd.com/read/38195439/white-spot-lesions-diagnosis-and-treatment-a-systematic-review
#30
JOURNAL ARTICLE
Pedro C Lopes, Teresa Carvalho, Ana T P C Gomes, Nelio Veiga, Letícia Blanco, Maria José Correia, Anna Carolina Volpi Mello-Moura
BACKGROUND: White spot lesions represent the first stage of caries and their prevalence has been increasing in recent years, particularly in patients undergoing orthodontic treatment. DIferential diagnosis and lesion activity are essential to decide on the clinical approaches to treatment. The aim of this study is to understand if the new diagnostic tools such as fluorescence, microradiography and computed microtomography have the potential to change the conventional treatment of white spots"...
January 9, 2024: BMC Oral Health
https://read.qxmd.com/read/38184822/establishment-and-characterization-of-a-highly-metastatic-hepatocellular-carcinoma-cell-line
#31
JOURNAL ARTICLE
Jiacheng Huang, Mengqing Sun, Menglan Wang, Anning Yu, Huilin Zheng, Chiwen Bu, Jie Zhou, Yu Zhang, Yiting Qiao, Zhenhua Hu
The prevalence of alcohol-related hepatocellular carcinoma (HCC) has been increasing during the last decade. Cancer research requires cell lines suitable for both in vitro and in vivo assays. However, there is a lack of cell lines with a high in vivo metastatic capacity for this HCC subtype. Herein, a new HCC cell line was established, named HCC-ZJ, using cells from a patient diagnosed with alcohol-related HCC. The karyotype of HCC-ZJ was 46, XY, del (p11.2). Whole-exome sequencing identified several genetic variations in HCC-Z that occur frequently in alcohol-associated HCC, such as mutations in TERT , CTNNB1 , ARID1A , CDKN2A , SMARCA2 , and HGF ...
December 2024: Bioengineered
https://read.qxmd.com/read/38178530/distinct-linear-polarization-of-core-shell-particles-at-near-backscattering-directions
#32
JOURNAL ARTICLE
Meng Li, Lei Bi, Wushao Lin
The degree of linear polarization (-P12 /P11 ) of scattered light by particles with a core-shell structure may display a distinct negative minimum at near-backscattering directions. However, the specific range of microphysical parameters within which this phenomenon occurs and the underlying physical mechanism are still unclear. Therefore, this study systematically investigated the impacts of particle size, shell-core ratio and refractive index on the negative minimum of -P12 /P11 at near-backscattering angles for both coated spheres and coated super-spheroids...
December 18, 2023: Optics Express
https://read.qxmd.com/read/38159712/microsatellite-markers-for-genotyping-of-kodamaea-ohmeri-demonstrating-outbreaks-based-on-a-multicenter-surveillance-study-in-china
#33
JOURNAL ARTICLE
Yanbing Li, Yuyan Huang, Mei Kang, Xiangyang Chen, Liwen Liu, Hongmei Zhao, Zhongju Chen, Meng Xiao, Yingchun Xu, Qiaolian Yi, Menglan Zhou
Kodamaea ohmeri, an emerging human pathogen, caused both sporadic and nosocomial infections among immunocompromised people with high mortality. However, there is limited research on the molecular epidemiology of K. ohmeri. A total of fifty microsatellite loci were designed based on K. ohmeri type strain NRRL Y-1932 and three loci were finally selected for microsatellite analysis. Non-duplicated K. ohmeri isolates and strains of other species were collected across China as a part of CHIF-NET program for sensitivity and specificity verification...
December 28, 2023: Infection, Genetics and Evolution
https://read.qxmd.com/read/38149542/antibody-reactivity-to-mycobacterium-tuberculosis-specific-regions-of-differences-1-and-regions-of-differences-9-proteins-and-peptides-in-rabbits-mice-and-humans
#34
JOURNAL ARTICLE
Shumaila N M Hanif, R Al-Attiyah, A S Mustafa
BACKGROUND: The major antigens encoded by Mycobacterium tuberculosis-specific genomic regions of differences (RDs) could be useful in the development of new vaccines and/or diagnostic reagents using T-cell and/or antibody assays. In particular, RD1 proteins PE35, PPE68, ESXA, ESXB, and RD9 protein ESXV and their peptides have been identified as major T-cell antigens. However, little is known about their antibody reactivities in different mammalian species. This study aims to determine the antigen-specific antibody reactivities to the above antigens and their peptides in three different mammalian species, i...
2023: International Journal of Mycobacteriology
https://read.qxmd.com/read/38137045/expanding-genotype-phenotype-correlation-in-2p11-2-p12-microdeletion-syndrome
#35
JOURNAL ARTICLE
Alessandra Ferrario, Nijas Aliu, Claudine Rieubland, Sébastian Vuilleumier, Hilary M Grabe, Pascal Escher
Chromosomal abnormalities on the short arm of chromosome 2 in the region p11.2 have been associated with developmental delay, intellectual disability, facial anomalies, abnormal ears, skeletal and genital malformations. Here we describe a patient with a de novo interstitial heterozygous microdeletion on the short arm of chromosome 2 in the region p11.2-p12. He presents with facial dysmorphism characterized by a broad and low root of the nose and low-set protruding ears. Clinical examinations during follow-up visits revealed congenital pendular nystagmus, decreased visual acuity and psychomotor development disorder including intellectual disability...
December 16, 2023: Genes
https://read.qxmd.com/read/38077073/-p-aeruginosa-controls-both-c-elegans-attraction-and-pathogenesis-by-regulating-nitrogen-assimilation
#36
Jacob G Marogi, Coleen T Murphy, Cameron Myhrvold, Zemer Gitai
Detecting chemical signals is important for identifying food sources and avoiding harmful agents. Like most animals, C. elegans use olfaction to chemotax towards their main food source, bacteria. However, little is known about the bacterial compounds governing C. elegans attraction to bacteria and the physiological importance of these compounds to bacteria. Here, we address these questions by investigating the function of a small RNA, P11, in the pathogen, Pseudomonas aeruginosa, that was previously shown to mediate learned pathogen avoidance...
November 29, 2023: bioRxiv
https://read.qxmd.com/read/38056049/clinical-whole-genome-sequencing-and-fish-identify-two-different-fusion-partners-for-nup98-in-a-patient-with-acute-myeloid-leukemia-a-case-report
#37
Bahareh A Mojarad, Zachary D Crees, Molly C Schroeder, Zhifu Xiang, Justin Vader, Jason Sina, Meagan Jacoby, John L Frater, Eric J Duncavage, David H Spencer, Kory Lavine, Julie A Neidich, Ina Amarillo
BACKGROUND: Only rare cases of acute myeloid leukemia (AML) have been shown to harbor a t(8;11)(p11.2;p15.4). This translocation is believed to involve the fusion of NSD3 or FGFR1 with NUP98; however, apart from targeted mRNA quantitative PCR analysis, no molecular approaches have been utilized to define the chimeric fusions present in these rare cases. CASE PRESENTATION: Here we present the case of a 51-year-old female with AML with myelodysplastic-related morphologic changes, 13q deletion and t(8;11), where initial fluorescence in situ hybridization (FISH) assays were consistent with the presence of NUP98 and FGFR1 rearrangements, and suggestive of NUP98/FGFR1 fusion...
January 2024: Cancer Genetics
https://read.qxmd.com/read/38005073/optimization-of-functional-toothpaste-formulation-containing-nano-hydroxyapatite-and-birch-extract-for-daily-oral-care
#38
JOURNAL ARTICLE
Alexandra-Diana Florea, Cristina Teodora Dobrota, Rahela Carpa, Csaba-Pal Racz, Gheorghe Tomoaia, Aurora Mocanu, Alexandra Avram, Olga Soritau, Lucian Cristian Pop, Maria Tomoaia-Cotisel
This research work aims to develop functional toothpastes with combined enamel remineralization and antibacterial effects using nano-hydroxyapatites (nHAPs) and birch extract. Eleven toothpastes (notated as P1-P11) were designed featuring different concentrations of birch extract and a constant concentration of pure nHAPs or substituted nHAPs (HAP-5%Zn, HAP-0.23%Mg-3.9%Zn-2%Si-10%Sr, and HAP-2.5%Mg-2.9%Si-1.34%Zn). In vitro assessments involved treating artificially demineralized enamel slices and analyzing surface repair and remineralization using Atomic Force Microscopy (AFM)...
November 13, 2023: Materials
https://read.qxmd.com/read/37994123/-prenatal-genetic-diagnosis-of-a-case-with-ring-chromosome-13
#39
JOURNAL ARTICLE
Lu Sun, Juan Wen, Guoming Chu, Guangrui Lai, Rong He
OBJECTIVE: To carry out cyto- and molecular genetic analysis for a fetus with a ring chromosome identified through non-invasive prenatal testing (NIPT). METHODS: A pregnant woman presented at the Shengjing Hospital Affiliated to China Medical University on May 11, 2021 was selected as the study subject. Maternal peripheral blood sample was screened by NIPT, and G-banded chromosomal karyotyping was carried out on amniotic fluid and peripheral blood samples from the couple...
December 10, 2023: Zhonghua Yi Xue Yi Chuan Xue za Zhi, Zhonghua Yixue Yichuanxue Zazhi, Chinese Journal of Medical Genetics
https://read.qxmd.com/read/37993435/reduction-of-p11-in-dorsal-raphe-nucleus-serotonergic-neurons-mediates-depression-like-behaviors
#40
JOURNAL ARTICLE
Wei Li, Zuqi Shen, Xuan Yin, Weiqi Chang, Xiaorong Chen, Jin Yu, Shifen Xu
The pathology of depression is related to the imbalance of various neurotransmitters. The dorsal raphe nucleus (DRN), the main brain region producing 5-HT, is crucially involved in the pathophysiology of depression. It contains several neuron types, in which GABAergic neurons are activated by stimuli associated with negative experiences and 5-HT neurons are activated by reward signals. However, little is known about its underlying molecular mechanisms. Here, we found that p11, a multifunctional protein associated with depression, was down-regulated by chronic social defeat stress in 5-HTDRN neurons...
November 22, 2023: Translational Psychiatry
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