Results 91 to 100 of about 82,236 (297)
, 2019 We provide an $O(n \log n)$ algorithm computing the linear maximum induced matching width of a tree and an optimal layout.
Svein Høgemo +2 more
openaire +2 more sources
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Autoinflammatory disorders (AIDs) are a clinically heterogeneous group of inborn errors of immunity primarily caused by dysregulation in the innate immune system. Clinical diagnosis is often challenging due to clinical heterogeneity and the overlapping phenotypes with other inborn errors of immunity and monogenic conditions that mimic AIDs ...
Vaishnavi Ashok Badiger +28 more
wiley +1 more source
Pracì Mìžnarodnogo Geometričnogo Centru, 2015 The notion of idempotent measure is a counterpart of that of probability measure in the idempotent mathematics. In this note, we consider a metric on the set of compact, idempotent measure spaces (mim-spaces) and prove that this space is separable and non-complete.
Brydun, Viktoriya +2 more
openaire +2 more sources
Toxicity of [C2mim]Cl to E. coli DH1 upon addition of [C2mim]Cl during exponential growth.
, 2014 Red: 0 mM [C2mim]Cl, purple: 50 mM [C2mim]Cl, blue: 100 mM [C2mim]Cl, green: 150 mM [C2mim]Cl, yellow: 200 mM [C2mim]Cl, orange: 400 mM [C2mim]Cl. Error bars represent standard errors.
Marijke Frederix (591031) +13 more
core +1 more source
A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Most pathogenic tubulin variants arise de novo in sporadic patients, causing severe brain malformations and significant neurodevelopmental impairment. The resulting reproductive disadvantage typically prevents these mutations from being transmitted to offspring.
Elena Cellini +9 more
wiley +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT CHARGE syndrome is a rare congenital disorder primarily attributed to heterozygous pathogenic variants of the CHD7 gene. Most pathogenic CHD7 variants are loss‐of‐function (LoF) variants, whereas the interpretation of missense variants remains challenging in the absence of functional evidence for their pathogenicity.
Takashi Okuno +8 more
wiley +1 more source
Push Pull Mooring dan Pyschological Ownership terhadap Perilaku Beralih Pengguna Instant Messaging
Indonesian Journal of Information Systems, 2019 Hasil survei tentang perilaku pengguna Mobile Instant Messaging (MIM) di Indonesia menjelaskan bahwa terjadi arus migrasi pengguna MIM. Perilaku beralih mengakibatkan penurunan pengguna dan profitabilitas layanan pada MIM yang ditinggalkan.
Vicky Djusmin, Raden Teduh Dirgahayu
doaj +1 more source
, 2012 In this work, we show that by using Metal-Insulator-Metal (MIM) structures integrated in series to the gateof submicron Metal-Oxide-Semiconductor Field-Effect Transistor (MOSFET) devices, highly-sensitive and ultra-lowpower consumption pH sensors can be ...
MARIA TERESA SANZ PASCUAL +5 more
core
, 2020 Introdução do livro "Orfeu Sem Mim", obra vencedora do Concurso de Poesia Joaquim Pessoa ...
Vila Maior, Dionísio
core
Systematic Review of Females With Intellectual Disability and MECP2 Duplication
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT MECP2 Duplication Syndrome (MDS) is a rare, X‐linked neurodevelopmental disorder typically affecting males. Females with MDS have been reported and are compiled here. We conducted a systematic review (PROSPERO CRD420250652426) of PubMed, EMBASE, and Google Scholar extracting individual participant data.
Paul Malik +10 more
wiley +1 more source