Results 1 to 10 of about 494 (136)

Clinical and Molecular Study of the NOG Gene in Families with Mandibular Micrognathism [PDF]

European Journal of Dentistry, 2021
AbstractObjectives Previous studies showed that noggin gene (NOG) sequence alterations, as well as epigenetic factors, could influence mandibular development. The aim of this study was to analyze clinical characteristics, NOG gene sequences, and promoter methylation sites in patients with mandibular micrognathism.Materials and Methods A total of 35 ...
Sandra Gutiérrez
exaly   +6 more sources

Genetic and Molecular Determinants of Familial Transmission of Skeletal Malocclusions. [PDF]

Orthod Craniofac Res
ABSTRACT Families studies conducted in different ethnic populations worldwide have helped elucidate the molecular and genetic factors involved in the development of skeletal class III malocclusion. Therefore, the aim of this study is to provide an updated summary.
Dehesa-Santos A, Carreño-Gomez L, Yañez-Vico R, Iglesias-Linares A.   +3 more
europepmc   +2 more sources

Congenital facial nerve palsy: Single center study [PDF]

Frontiers in Pediatrics, 2023
ObjectivesThis study will list the most common comorbidities of congenital facial nerve palsy and how to detect and treat them, with special attention for ENT-problems such as hearing loss.
Hermine Baelen, Hermine Baelen, Anne-Marie Esschendal, Yannick De Brucker, Ina Foulon, Ina Foulon, Vedat Topsakal, Vedat Topsakal, Frans Gordts, Frans Gordts   +9 more
doaj   +2 more sources

Prenatal diagnosis of micrognathia and postnatal identification of cleft soft palate: A case report [PDF]

Radiology Case Reports
This case report details the prenatal diagnosis of fetal micrognathia using advanced ultrasound techniques and highlights its role in anomaly detection and perinatal management.
Saburi Singhania, Shivali Kashikar, Vaishali Dhawan, Pratapsingh Parihar   +3 more
doaj   +2 more sources

Differential gene expression profiling reveals potential biomarkers and pharmacological compounds against SARS-CoV-2: Insights from machine learning and bioinformatics approaches

Frontiers in Immunology, 2022
The COVID-19 pandemic, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has created an urgent global situation. Therefore, it is necessary to identify the differentially expressed genes (DEGs) in COVID-19 patients to understand ...
M. Nazmul Hoque, Md. Murshed Hasan Sarkar, Md. Arif Khan, Md. Arif Khan, Md. Arju Hossain, Md. Imran Hasan, Md. Habibur Rahman, Md. Ahashan Habib, Shahina Akter, Tanjina Akhtar Banu, Barna Goswami, Iffat Jahan, Tasnim Nafisa, Md. Maruf Ahmed Molla, Mahmoud E. Soliman, Yusha Araf, Yusha Araf, M. Salim Khan, Chunfu Zheng, Chunfu Zheng, Tofazzal Islam   +20 more
doaj   +2 more sources

Bilateral mandibular distraction in micrognathism or hypoplasia of mandible, hazrat fatemeh hospital

Journal of Acute Disease, 2014
Objective: To determine the results of Bilateral Distraction Osteogenesis (DO) versus traditional methods in treatment of micrognathia. Methods: During 6 years we had 67 patients with micrognathia.
Hamid Karimi
exaly   +3 more sources

Single Nucleotide Polymorphisms (SNPs) of COL1A1 and COL11A1 in Class II Skeletal Malocclusion of Ethnic Javanese Patient [PDF]

Clinical, Cosmetic and Investigational Dentistry, 2020
I Gusti Aju Wahju Ardani,1 Aulanni’am,2 Indeswati Diyatri3 1Orthodontics Department, Faculty of Dental Medicine, Airlangga University, Surabaya, Indonesia; 2Biochemistry Department, Faculty of Veterinary Medicine, Brawijaya University, Malang ...
Ardani IGAW, Aulanni'am, Diyatri I
doaj   +2 more sources

Shprintzen-goldberg craniosynostosis: craniofacial and oral characteristics, diagnosis, and clinical management of a very rare syndrome

RGO: Revista Gaúcha de Odontologia, 2022
Shprintzen-Goldberg craniosynostosis syndrome, characterized by craniosynostosis and marfanoid habitus, is a very rare entity described in 75 individuals worldwide.
Danielle Monsores VIEIRA, Florense Gabriela SILVA, Michele Baffi DINIZ, Maria Cristina Duarte FERREIRA, Maria Teresa Botti Rodrigues dos SANTOS, Renata Oliveira GUARÉ   +5 more
doaj   +1 more source

Reliable Identification and Interpretation of Single‐Cell Molecular Heterogeneity and Transcriptional Regulation using Dynamic Ensemble Pruning

Advanced Science, Volume 10, Issue 22, August 4, 2023., 2023
A dynamic ensemble pruning framework (DEPF) is proposed to identify and interpret single‐cell molecular heterogeneity. In particular, a silhouette coefficient‐based indicator is developed and evaluated to determine the optimization direction of the bi‐objective function.
Yi Fan, Yunhe Wang, Fuzhou Wang, Lei Huang, Yuning Yang, Ka‐Chun Wong, Xiangtao Li   +6 more
wiley   +1 more source

A case of severe type of cerebro-costo-mandibular syndrome [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2016
Introduction. Cerebro-costo-mandibular syndrome (CCMS) is a rare disorder, with only 75 cases described in the literature to date. CCMS is characterized by association of micrognathia and specific multiple rib defects.
Matić Aleksandra, Velisavljev-Filipović Gordana, Lovrenski Jovan, Gajdobranski Đorđe   +3 more
doaj   +1 more source