Results 121 to 130 of about 63,568 (308)

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone, Freddy Chafota, Miguel E. Rentería, Randi J. Hagerman, Ellery Santos, Anna Atkinson, Nicholas G. Martin, Elsdon Storey, Danuta Z. Loesch   +8 more
wiley   +1 more source

Genotypic variability for root nodulation and identification of high yielding chickpea (Cicer arietinum L.) genotypes

Electronic Journal of Plant Breeding
Evaluating diverse chickpea genotypes for growth, root nodule, and yield parameters can provide valuable insights to identify genotypes with desirable traits for improved crop production.
Jyoti Kumari, Rafat Sultana*, Zafar Imam, Mankesh Kumar and Reena Kumari
doaj   +1 more source

Phenotypic and Genotypic Correlation and Path Coefficients in Rainfed Upland Rice (Oryza sativa L.) Genotypes at Guraferda, Southwest Ethiopia

, 2018
A field experiment was conducted with the objective of determining the magnitude of association between yield and yield component characters. Fifteen rainfed upland rice genotypes were evaluated in randomized complete block design in three replications ...
Kampe, Abayneh Kacharo
core  

Genotypic phenotypic correlation in male breast cancer [PDF]

, 2018
© 2018 Dr. Siddhartha DebMale breast cancers (MBCs) are rare cancers, comprising less than 1% of all breast cancers and less than 1% of all cancers in men.
Deb, Siddhartha
core  

Genotypic prediction of HIV-1 subtype D tropism.

, 2011
International audienceUNLABELLED: ABSTRACT: BACKGROUND: HIV-1 subtype D infections have been associated with rapid disease progression and phenotypic assays have shown that CXCR4-using viruses are very prevalent.
Jacques Izopet, Delobel, Pierre, Patrick Bruel, Bruel, Patrick, Pierre Delobel, Marie-Laure Chaix, Raymond, Stéphanie, Bruno Marchou, Sandres-Sauné, Karine, Michelle Cazabat, Karine Sandres-Sauné, Patrice Massip, Marchou, Bruno, Chaix, Marie-Laure, Massip, Patrice, Stéphanie Raymond, Izopet, Jacques, Stéphanie Encinas, Cazabat, Michelle, Encinas, Stéphanie   +19 more
core   +1 more source

High‐Resolution MRI Revealed Different Etiology‐Specific Associations With Cerebral Infarction in Adult Moyamoya Vasculopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐resolution MRI enables detailed assessment of intracranial vessel wall pathology in moyamoya vasculopathy. We aimed to classify adult moyamoya vasculopathy etiologies using high‐resolution MRI and to examine subtype‐specific associations between high‐resolution MRI features and ischemic infarction.
Guangsong Han, Jiachun Pan, Yuehui Hong, Xiaoyuan Fan, Ming Yao, Lixin Zhou, Yicheng Zhu, Feng Feng, Jun Ni   +8 more
wiley   +1 more source

Genotype-Environment Correlation in the Era of DNA [PDF]

Behavior Genetics, 2014
One of John Loehlin's many contributions to the field of behavioral genetics involves gene-environment (GE) correlation. The empirical base for GE correlation was research showing that environmental measures are nearly as heritable as behavioral measures and that genetic factors mediate correlations between environment and behavior.
openaire   +4 more sources

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

Correlation between phenotypic (LPT) and genotypic (sequencing) amitraz resistance status.

, 2015
Discriminating dose of amitraz used was 250 ppm.a Larvae that were alive after the larval packet test assay was completed, meaning they were resistant to the amitraz concentrations applied.b Larvae that were susceptible to the concentrations of amitraz ...
Nicolaas A. van der Merwe (671342), Samantha Baron (767600), Maxime Madder (513977), Christine Maritz-Olivier (767601)   +3 more
core   +1 more source

Movement Disorders in Aicardi–Goutières Syndrome and Response to Immunomodulation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study characterizes movement disorders and treatment responses in seven children with Aicardi–Goutières syndrome (AGS). We retrospectively evaluated motor phenotypes, neuroimaging, and interferon signatures in patients treated with baricitinib or anifrolumab. Spasticity affected all patients, while dystonia was present in 4/7.
Enrique Gonzalez Saez‐Diez, Monica Ferrer Socorro, Kathryn Yang, Nicole Battaglia, Zainab Zaman, Mariko Bennett, Adeline Vanderver, Pui Y. Lee, Lauren A. Henderson, Milena M. Andzelm, Darius Ebrahimi‐Fakhari   +10 more
wiley   +1 more source