Search research articles
Contact Us
Filters
Showing results (1-10 of 22) with videos related to
Page
of 3
Sort By:
Molecular Genetics and Genomics : MGG
|
August 8, 2022
A missense mutation in TTC8/BBS8 affecting mRNA splicing in patients with non-syndromic retinitis pigmentosa
Shiwali Goyal, Vanita Vanita
Diabetes/Metabolism Research and Reviews
|
January 2, 2025
The Rise of Type 2 Diabetes in Children and Adolescents: An Emerging Pandemic
Shiwali Goyal, Vanita Vanita
Current Diabetes Reviews
|
January 19, 2021
Genetic and Non-genetic Determinants of Cardiovascular Disease in South Asians
Shiwali Goyal, Dharambir K Sanghera
Stem Cell Reviews and Reports
|
July 16, 2025
Gene and Stem Cell-Based Therapies for Retinal Degenerative Diseases: Update, Challenges, and Future Directions
Mohd Akbar Bhat, Shiwali Goyal
Biochemical Genetics
|
March 9, 2022
Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms with Coronary Artery Disease in North Indian Punjabi Population
Mohd Akbar Bhat, Jatinder Singh, Shiwali Goyal
Clinical & Experimental Ophthalmology
|
January 29, 2020
Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin
Shiwali Goyal, Indu R Singh, Vanita Vanita
Molecular Biology Reports
|
September 26, 2025
A 15 bp non-canonical splice-site deletion in ABCA4 linked with retinitis pigmentosa and myopia: insights into splicing defects and phenotypic variability
Vanita Vanita, Shiwali Goyal, Indu R Singh
World Journal of Clinical Pediatrics
|
June 10, 2025
Genetic and environmental factors contributing to anophthalmia and microphthalmia: Current understanding and future directions
Shiwali Goyal, Shailja Tibrewal, Ria Ratna, et al.
BMC Ophthalmology
|
May 11, 2023
A nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India
Shiwali Goyal, Kabir Singh, Aashna Uppal, et al.
Frontiers in Pediatrics
|
December 19, 2022
Molecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in <i>GJA8</i> and <i>GJA3</i>
Vanita Vanita, Shiwali Goyal, Shailja Tibrewal, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Molecular Genetics and Genomics : MGG
|
August 8, 2022
A missense mutation in TTC8/BBS8 affecting mRNA splicing in patients with non-syndromic retinitis pigmentosa
Shiwali Goyal, Vanita Vanita
Diabetes/Metabolism Research and Reviews
|
January 2, 2025
The Rise of Type 2 Diabetes in Children and Adolescents: An Emerging Pandemic
Shiwali Goyal, Vanita Vanita
Current Diabetes Reviews
|
January 19, 2021
Genetic and Non-genetic Determinants of Cardiovascular Disease in South Asians
Shiwali Goyal, Dharambir K Sanghera
Stem Cell Reviews and Reports
|
July 16, 2025
Gene and Stem Cell-Based Therapies for Retinal Degenerative Diseases: Update, Challenges, and Future Directions
Mohd Akbar Bhat, Shiwali Goyal
Biochemical Genetics
|
March 9, 2022
Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms with Coronary Artery Disease in North Indian Punjabi Population
Mohd Akbar Bhat, Jatinder Singh, Shiwali Goyal
Clinical & Experimental Ophthalmology
|
January 29, 2020
Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin
Shiwali Goyal, Indu R Singh, Vanita Vanita
Molecular Biology Reports
|
September 26, 2025
A 15 bp non-canonical splice-site deletion in ABCA4 linked with retinitis pigmentosa and myopia: insights into splicing defects and phenotypic variability
Vanita Vanita, Shiwali Goyal, Indu R Singh
World Journal of Clinical Pediatrics
|
June 10, 2025
Genetic and environmental factors contributing to anophthalmia and microphthalmia: Current understanding and future directions
Shiwali Goyal, Shailja Tibrewal, Ria Ratna, et al.
BMC Ophthalmology
|
May 11, 2023
A nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India
Shiwali Goyal, Kabir Singh, Aashna Uppal, et al.
Frontiers in Pediatrics
|
December 19, 2022
Molecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in <i>GJA8</i> and <i>GJA3</i>
Vanita Vanita, Shiwali Goyal, Shailja Tibrewal, et al.
Page
of 3