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International Journal of Molecular Sciences|October 27, 2019
Insights on Calcium-Dependent Protein Kinases (CPKs) Signaling for Abiotic Stress Tolerance in PlantsRana Muhammad Atif, Luqman Shahid, Muhammad Waqas, et al.
Genes|April 28, 2023
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial PolydactylySafeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, et al.
Functional & Integrative Genomics|September 12, 2023
Genome-wide association studies: an intuitive solution for SNP identification and gene mapping in treesM N Ashwath, Shivaji Ajinath Lavale, A V Santhoshkumar, et al.
Frontiers in Genetics|December 1, 2022
Progress and prospectus in genetics and genomics of Phytophthora root and stem rot resistance in soybean (Glycine max L.)Subhash Chandra, Mukesh Choudhary, Pravin K Bagaria, et al.
Journal of Human Genetics|October 29, 2019
Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairmentKhurram Liaqat, Shabir Hussain, Muhammad Bilal, et al.
Journal of Human Genetics|December 3, 2021
Novel variants in the LRP4 underlying Cenani-Lenz Syndactyly syndromeHammal Khan, Angie En Qi Chong, Muhammad Bilal, et al.
The International Journal of Biochemistry & Cell Biology|July 18, 2018
Molecular and in silico analyses validates pathogenicity of homozygous mutations in the NPR2 gene underlying variable phenotypes of Acromesomelic dysplasia, type MaroteauxIrfanullah, Amir Zeb, Naila Shinwari, et al.
Human Genetics|July 5, 2018
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Khurram Liaqat, et al.
Molecules (Basel, Switzerland)|December 10, 2021
Secondary Metabolite Profiling, Anti-Inflammatory and Hepatoprotective Activity of Neptunia triquetra (Vahl) BenthNasir Aziz Wagay, Shah Rafiq, Mohammad Aslam Rather, et al.
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