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Experimental Eye Research
|
March 21, 2016
Genetic analysis of consanguineous families presenting with congenital ocular defects
Ehsan Ullah, Muhammad Arif Nadeem Saqib, Sundus Sajid, et al.
Archiv Der Pharmazie
|
July 25, 2019
Densely substituted piperidines as a new class of elastase inhibitors: Synthesis and molecular modeling studies
Syeda S Hamdani, Bilal A Khan, Aamer Saeed, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2025
REASONING BEYOND ACCURACY: EXPERT EVALUATION OF LARGE LANGUAGE MODELS IN DIAGNOSTIC PATHOLOGY
Asim Waqas, Asma Khan, Zarifa Gahramanli Ozturk, et al.
Journal of Lipid Research
|
February 5, 2025
A multi-ancestry genome-wide association study and evaluation of polygenic scores of LDL-C levels
Umm-Kulthum Ismail Umlai, Salman M Toor, Yasser A Al-Sarraj, et al.
Journal of Nanobiotechnology
|
July 16, 2022
Protective role of small extracellular vesicles derived from HUVECs treated with AGEs in diabetic vascular calcification
Bei Guo, Su-Kang Shan, Feng Xu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 10, 2020
A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis
Elena R Schiff, Malena Daich Varela, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science
|
September 13, 2018
Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa
Zahid Latif, Imen Chakchouk, Isabelle Schrauwen, et al.
Scientific Reports
|
October 7, 2016
Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum
Maleeha Maria, Ideke J C Lamers, Miriam Schmidts, et al.
Human Mutation
|
March 10, 2022
Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study
Robert B Hufnagel, Wendi Liang, Jacque L Duncan, et al.
Frontiers in Cardiovascular Medicine
|
June 9, 2022
Cellular Crosstalk in the Vascular Wall Microenvironment: The Role of Exosomes in Vascular Calcification
Yun-Yun Wu, Su-Kang Shan, Xiao Lin, et al.
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Search research articles
Search
Showing results (211-220 of 233) with videos related to
Sort By:
Page
of 24
Experimental Eye Research
|
March 21, 2016
Genetic analysis of consanguineous families presenting with congenital ocular defects
Ehsan Ullah, Muhammad Arif Nadeem Saqib, Sundus Sajid, et al.
Archiv Der Pharmazie
|
July 25, 2019
Densely substituted piperidines as a new class of elastase inhibitors: Synthesis and molecular modeling studies
Syeda S Hamdani, Bilal A Khan, Aamer Saeed, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2025
REASONING BEYOND ACCURACY: EXPERT EVALUATION OF LARGE LANGUAGE MODELS IN DIAGNOSTIC PATHOLOGY
Asim Waqas, Asma Khan, Zarifa Gahramanli Ozturk, et al.
Journal of Lipid Research
|
February 5, 2025
A multi-ancestry genome-wide association study and evaluation of polygenic scores of LDL-C levels
Umm-Kulthum Ismail Umlai, Salman M Toor, Yasser A Al-Sarraj, et al.
Journal of Nanobiotechnology
|
July 16, 2022
Protective role of small extracellular vesicles derived from HUVECs treated with AGEs in diabetic vascular calcification
Bei Guo, Su-Kang Shan, Feng Xu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 10, 2020
A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis
Elena R Schiff, Malena Daich Varela, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science
|
September 13, 2018
Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa
Zahid Latif, Imen Chakchouk, Isabelle Schrauwen, et al.
Scientific Reports
|
October 7, 2016
Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum
Maleeha Maria, Ideke J C Lamers, Miriam Schmidts, et al.
Human Mutation
|
March 10, 2022
Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study
Robert B Hufnagel, Wendi Liang, Jacque L Duncan, et al.
Frontiers in Cardiovascular Medicine
|
June 9, 2022
Cellular Crosstalk in the Vascular Wall Microenvironment: The Role of Exosomes in Vascular Calcification
Yun-Yun Wu, Su-Kang Shan, Xiao Lin, et al.
Page
of 24