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Human Genomics
|
November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority population
LéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
Angewandte Chemie (International Ed. in English)
|
September 8, 2024
Dipole Moment Modulation of Terminal Groups Enables Asymmetric Acceptors Featuring Medium Bandgap for Efficient and Stable Ternary Organic Solar Cells
Bosen Zou, Anhai Liang, Pengbo Ding, et al.
Advanced Genetics (Hoboken, N.J.)
|
December 30, 2024
Extreme Phenotypic Variability of <i>ACTG1</i>-Related Disorders in Hearing Loss
Maria T Bernardi, Memoona Ramzan, Laura Calderon, et al.
Scientific Reports
|
January 17, 2025
Role of transforming growth factor-β1 in regulating adipocyte progenitors
Nguyen Quynh Phuong, Muhammad Bilal, Allah Nawaz, et al.
Advanced Materials (Deerfield Beach, Fla.)
|
May 28, 2024
Precisely Controlling Polymer Acceptors with Weak Intramolecular Charge Transfer Effect and Superior Coplanarity for Efficient Indoor All-Polymer Solar Cells with over 27% Efficiency
Bosen Zou, Ho Ming Ng, Han Yu, et al.
Scientific Reports
|
October 22, 2025
Tofogliflozin ameliorates cardiotoxin induced skeletal muscle injury and fibrosis in obesity
Muhammad Bilal, Nguyen Quynh Phuong, Tomonobu Kado, et al.
Human Molecular Genetics
|
June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humans
Zohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
NPJ Genomic Medicine
|
March 26, 2025
Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension
Sofia Karl, Ekkehard Grünig, Memoona Shaukat, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
June 19, 2026
Deletion of Tgf-β1 From CD206<sup>+</sup> M2 Macrophages Ameliorates Obesity-Induced Suppression of Myogenesis and AMPK Phosphorylation in Skeletal Muscle
Muhammad Bilal, Le Duc Anh, Nguyen Quynh Phuong, et al.
Human Mutation
|
July 15, 2021
Variants of human CLDN9 cause mild to profound hearing loss
Memoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
Page
of 25
Search research articles
Search
Showing results (221-230 of 241) with videos related to
Sort By:
Page
of 25
Human Genomics
|
November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority population
LéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
Angewandte Chemie (International Ed. in English)
|
September 8, 2024
Dipole Moment Modulation of Terminal Groups Enables Asymmetric Acceptors Featuring Medium Bandgap for Efficient and Stable Ternary Organic Solar Cells
Bosen Zou, Anhai Liang, Pengbo Ding, et al.
Advanced Genetics (Hoboken, N.J.)
|
December 30, 2024
Extreme Phenotypic Variability of <i>ACTG1</i>-Related Disorders in Hearing Loss
Maria T Bernardi, Memoona Ramzan, Laura Calderon, et al.
Scientific Reports
|
January 17, 2025
Role of transforming growth factor-β1 in regulating adipocyte progenitors
Nguyen Quynh Phuong, Muhammad Bilal, Allah Nawaz, et al.
Advanced Materials (Deerfield Beach, Fla.)
|
May 28, 2024
Precisely Controlling Polymer Acceptors with Weak Intramolecular Charge Transfer Effect and Superior Coplanarity for Efficient Indoor All-Polymer Solar Cells with over 27% Efficiency
Bosen Zou, Ho Ming Ng, Han Yu, et al.
Scientific Reports
|
October 22, 2025
Tofogliflozin ameliorates cardiotoxin induced skeletal muscle injury and fibrosis in obesity
Muhammad Bilal, Nguyen Quynh Phuong, Tomonobu Kado, et al.
Human Molecular Genetics
|
June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humans
Zohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
NPJ Genomic Medicine
|
March 26, 2025
Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension
Sofia Karl, Ekkehard Grünig, Memoona Shaukat, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
June 19, 2026
Deletion of Tgf-β1 From CD206<sup>+</sup> M2 Macrophages Ameliorates Obesity-Induced Suppression of Myogenesis and AMPK Phosphorylation in Skeletal Muscle
Muhammad Bilal, Le Duc Anh, Nguyen Quynh Phuong, et al.
Human Mutation
|
July 15, 2021
Variants of human CLDN9 cause mild to profound hearing loss
Memoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
Page
of 25