Results 181 to 190 of about 41,964 (225)

Developing early intervention/support services for deaf children and their families [PDF]

, 2002

core  

Caenorhabditis elegans as an in vivo model system for human inherited primary arrhythmia syndromes

The Journal of Physiology, EarlyView.
Abstract figure legend Most genes involved in inherited primary arrhythmia syndromes (IPAS) are conserved in Caenorhabditis elegans, where genetic manipulation enables functional characterization of variants, identification of regulatory proteins, and in vivo drug testing.
Antoine Delinière, Thomas Boulin, Maëlle Jospin, Alexandre Janin, Gilles Millat, Philippe Chevalier, Olga Andrini   +6 more
wiley   +1 more source

Birth of a Language in the Backlands of Brazil. [PDF]

Cogn Sci
Almeida-Silva A, Nitschke R, Valls Yoshida F, Nóbrega V, Miyagawa S.   +4 more
europepmc   +1 more source

Neurophysiological sensitivity to envelope and pulse timing interaural time differences in cochlear implanted rats with different hearing experiences

The Journal of Physiology, EarlyView.
Abstract figure legend Graphical summary of our study. Rats with varying hearing experiences were bilaterally implanted with cochlear implants (CIs), and neural responses were recorded from the inferior colliculus (IC), an auditory midbrain region (left).
S. Fang, T. Fleiner, F. Peng, S. Buchholz, M. Zeeshan, N. Rosskothen‐Kuhl, J. W. Schnupp   +6 more
wiley   +1 more source

Understanding the decision of parents to opt‐out of medically actionable secondary findings offered through genome sequencing

Journal of Genetic Counseling, Volume 35, Issue 3, June 2026.
Abstract Genomic sequencing (GS) for patients and families with rare disease creates the opportunity for precise diagnosis as well as the option to learn about medically actionable secondary findings (SF). Debate persists internationally on how to manage the analysis and disclosure of SF, especially in settings where service delivery models for GS are ...
Abigail Hansen, Stephanie Luca, Olivia Moran, Riyana Babul‐Hirji, Teresa B. Coe, Kalin Wilk, Daniel Assamad, Katharine Fooks, Viji Venkataramanan, Salma Shickh, Joyce Yan, Vercancy Wu, Lauren Badalato, Tugce B. Balci, Virginie Beausejour Ladouceur, Lauren Chad, Caitlin Chisholm, Meredith K. Gillespie, Lijia Huang, Olga Jarinova, Lynette Lau, Whiwon Lee, Michael P. Mackley, Christian R. Marshall, Roberto Mendoza‐Londono, Chantal F. Morel, Julie Richer, Sarah Sawyer, Dimitrios James Stavropoulos, Anna Szuto, Mark Tarnopolsky, Anita Villani, Laura Zahavich, Martin J. Somerville, Kym M. Boycott, Wendy J. Ungar, Robin Z. Hayeems   +36 more
wiley   +1 more source

Neural associations between fingerspelling, print, and signs: An ERP priming study with deaf readers. [PDF]

Brain Lang
Lee B, Ortega SE, Martinez PM, Midgley KJ, Holcomb PJ, Emmorey K.   +5 more
europepmc   +1 more source

Functional reassessment of extended splice region variants in MYO7A with hearing loss and Usher syndrome

The Journal of Pathology, Volume 269, Issue 2, Page 222-231, June 2026.
Abstract MYO7A is a causal gene, underlying Usher syndrome type 1B (USH1B) and both autosomal recessive (DFNB2) and dominant (DFNA11) non‐syndromic hearing loss. Despite the large number of reported MYO7A variants (over 2,200), variants located in an extended splice region remain difficult to interpret and are often classified as variants of uncertain ...
Tao Shi, Yu Huang, Xiaohuan Su, Lisheng Yu, Yixin Zhao, Jing Cheng   +5 more
wiley   +1 more source

Reading ability in both deaf and hearing adults is linked to neural representations of abstract phonology derived from visual speech

Evans S, Price CJ, Diedrichsen J, Twomey T, Beedie I, Fraser M, MacSweeney M.   +6 more
europepmc   +1 more source

Delayed First Language Exposure Negatively Impacts Representation of Small Quantities: Evidence from Deaf and Hard-of-Hearing Children. [PDF]

Open Mind (Camb)
Quam M, Carrigan E, Walker K, Shusterman A, Coppola M.   +4 more
europepmc   +1 more source