Results 111 to 120 of about 248,402 (331)

An ITPR1 Variant in the IP3‐ITPR1 Binding Pocket Associated With a Clinical Phenotype of Athetoid Cerebral Palsy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT A de novo, missense variant in ITPR1‐inositol 1,4,5‐trisphosphate receptor type 1 (ITPR1), p.(Tyr567Cys), was identified by trio whole‐genome sequencing in an individual diagnosed with Spinocerebellar ataxia 29 (SCA29) who was affected by cerebral palsy and global developmental delay.
Thania Ordaz, Jagadish Chandrabose Sundaramurthi, Adam S. Arterbery, Anita M. Bagley, Michael A Gargano, Jeremy P Bauer, Daniel Danis, Philip Giampietro, Ellen Raney, Lauren Rekerle, Mallory Shingle, Jon R. Davids, Peter N. Robinson   +12 more
wiley   +1 more source

DETERMINANTAL IDENTITIES FOR k LUCAS SEQUENCE

Journal of New Theory, 2016
Abstaract−In this paper, we defined new relationship between k Lucas sequences and determi- nants of their associated matrices, this approach is different and never tried in k Fibonacci sequence ...
Ashok Dnyandeo Godase, Machindra Baban Dhakne   +1 more
doaj  

On Diophantine equations involving Lucas sequences

Open Mathematics, 2019
In this paper, we shall study the Diophantine equation un = R(m)P(m)Q(m), where un is a Lucas sequence and R, P and Q are polynomials (under weak assumptions).
Trojovský Pavel
doaj   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

On some identities for the DGC Leonardo sequence [PDF]

Notes on Number Theory and Discrete Mathematics
In this study, we examine the Leonardo sequence with dual-generalized complex (DGC) coefficients for 𝔭∈ℝ. Firstly, we express some summation formulas related to the DGC Fibonacci, DGC Lucas, and DGC Leonardo sequences.
Çiğdem Zeynep Yılmaz, Gülsüm Yeliz Saçlı   +1 more
doaj   +1 more source

Geometric Aspects of Lucas Sequences, I

Tokyo Journal of Mathematics, 2020
This article is a sequel of $\langle$Geometric aspects of Lucas sequences, I$\rangle$, which presents a way of viewing Lucas sequences in the framework of group scheme theory. This enables us to treat the Lucas sequences from a geometric and functorial viewpoint, which was suggested by Laxton $\langle$On groups of linear recurrences, I$\rangle$ and by ...
openaire   +3 more sources

A Dynamical Property Unique to the Lucas Sequence

The Fibonacci Quarterly, 2001
9 ...
Puri, Y., Ward, T.
openaire   +2 more sources

The Politics of Framing the Student Problem: Inquiries Into Australian Civics Education, 2006–2024

Australian Journal of Social Issues, EarlyView.
ABSTRACT Recurring debates about civics, the kinds of history that should, and should not, be taught in school, and ‘standards debates’ about the ‘basics’ typically follow on the heels of recurring moral panics about the ‘declining’ state of ‘our’ education system.
Patrick O'Keeffe, Judith Bessant, Madeline Drake   +2 more
wiley   +1 more source

On Squares in Lucas Sequences

, 2013
In this short paper, we prove, by only using elementary tools, general cases when $U_n(P,Q) \neq \square$, where $U_n(P,Q)$ is the Lucas sequence of the first type.
openaire   +2 more sources

Establishment and molecular profiling of a PDX model of a metachronous brain tumor in a patient with constitutional mismatch repair deficiency with biallelic MSH6 variant

Animal Models and Experimental Medicine, EarlyView.
A 6½‐year‐old girl was diagnosed with a medulloblastoma, SHH activated, subtype 3 and TP53 mutant (somatic). After surgery and chemotherapy, she was monitored with quarterly magnetic resonance imaging (MRI) scans and remained free of disease for almost 4 years.
Daniel Antunes Moreno, Bruna Minniti Mançano, Mirella Baroni, Eric Allison Philot, Felipe Antonio de Oliveira Garcia, Murilo Bonatelli, Flávia Escremim de Paula, Iara Viana Vidigal Santana, Gustavo Ramos Teixeira, Mauricio Yamanari, Luciane Sussuchi da Silva, André Escremim de Paula, Augusto Perazzolo Antoniazzi, Adrian Willig, Xiaobin Xing, Zhenyu Xu, Lucas Lourenço, Carlos Almeida Junior, Silvia Aparecida Teixeira, Rui Manuel Reis   +19 more
wiley   +1 more source