Results 141 to 150 of about 1,982,012 (407)
Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison +3 more
wiley +1 more source
Journal of Pharmacy and Bioallied SciencesBackground: An adjuvant treatment, known as low-level laser therapy (LLLT), has been suggested to quicken orthodontic tooth movement and perhaps shorten the course of treatment. Materials and Methods: For 60 orthodontic patients aged between 15 and 25, a
Mohammad K. Alam +4 more
doaj +1 more source
Dental Journal, 2017 Background: Orthodontic tooth movement is a continual and balanced process between bone deposition and bone resorption in pressure and tension sites. Stichopus hermanii is one of the best fishery commodities in Indonesia.
Noengki Prameswari, Arya Brahmanta
doaj +1 more source
Divergent functional traits in three sympatric Arctic charr Salvelinus alpinus morphs are not coupled with the age of the lineage divergence [PDF]
, 2016 Three genetically discrete morphs of Arctic charr in Loch Rannoch, Scotland originated from a recent divergence within the lake (in situ) (piscivore and benthivore morphs) and from secondary contact of two older lineages (ex situ; a planktivore–piscivore/
Adams, Colin +4 more
core +2 more sources
Orthodontics & craniofacial research, 2019 The concept of fabricating aligners on setup casts for orthodontic tooth movement dates back to 19451 . Nowadays, the increasing demand for invisible orthodontics and aesthetic considerations, primarily across adult patients, has made the use of ...
Anna Iliadi +2 more
semanticscholar +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Heterozygous pathogenic variants in TBX3 cause Ulnar‐Mammary syndrome (UMS). The phenotype is classically characterized by upper limb defects, apocrine/mammary gland hypoplasia, hypogonadism, and various midline defects. However, the clinical spectrum is highly variable, and some individuals may present with a mild or atypical presentation ...
Ziv Halperin, Karin Weiss
wiley +1 more source
Machining of wood using a Rip Tooth: effects of work-piece variations on cutting mechanics [PDF]
, 2011 Genetics and environmental conditions during the growth of wood are known to affect the intrinsic characteristics influencing cutting mechanics.
Clahr, Emil +2 more
core
Meeting report: a hard look at the state of enamel research. [PDF]
, 2017 The Encouraging Novel Amelogenesis Models and Ex vivo cell Lines (ENAMEL) Development workshop was held on 23 June 2017 at the Bethesda headquarters of the National Institute of Dental and Craniofacial Research (NIDCR).
Bartlett, John D +13 more
core +1 more source
De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil +8 more
wiley +1 more source
Alveolar Bone Formation by Orthodontic Movement
Česká Stomatologie a Praktické Zubní Lékařství, 2012 Objectives: The ability to move tooth trough alveolar bone is one of the basic principles in orthodontics. Mechanical force generated by orthodontic appliance is transferred to periodontal ligament resulting in the remodeling of alveolar bone.
M. Šedivec +2 more
doaj +1 more source