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Investigative Ophthalmology & Visual Science
|
January 8, 2010
Mutation discovered in a feline model of human congenital retinal blinding disease
Marilyn Menotti-Raymond, Koren Holland Deckman, Victor David, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
February 5, 2020
Maternal variants within the apolipoprotein L1 gene are associated with preeclampsia in a South African cohort of African ancestry
Semone Thakoordeen-Reddy, Cheryl Winkler, Jagidesa Moodley, et al.
Veterinary Ophthalmology
|
September 16, 2009
Retinal degeneration in the Abyssinian and Somali cat (rdAc): correlation between genotype and phenotype and rdAc allele frequency in two continents
Kristina Narfström, Victor David, Oswald Jarret, et al.
Frontiers in Molecular Biosciences
|
December 20, 2021
Structure-Function Relationship of the Disintegrin Family: Sequence Signature and Integrin Interaction
Ariana A Vasconcelos, Jorge C Estrada, Victor David, et al.
Zoological Letters
|
February 27, 2025
Potential of Garra rufa as a novel high-temperature resistant model fish: a review on current and future approaches
Yasuhito Shimada, Baki Aydın, Koto Kon-Nanjo, et al.
Scientific Data
|
May 9, 2025
Chromosome-level genome assembly of the doctor fish (Garra rufa)
Tetsuo Kon, Koto Kon-Nanjo, Kiki Syaputri Handayani, et al.
Toxins
|
August 9, 2018
Recombinant and Chimeric Disintegrins in Preclinical Research
Victor David, Barbara Barbosa Succar, João Alfredo de Moraes, et al.
The Journal of Heredity
|
March 13, 2014
Development of MHC-Linked Microsatellite Markers in the Domestic Cat and Their Use to Evaluate MHC Diversity in Domestic Cats, Cheetahs, and Gir Lions
Katrina M Morris, Katherine Kirby, Julia A Beatty, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 6, 2021
Association of GSTM1 Deletion With Progression of CKD in Children: Findings From the Chronic Kidney Disease in Children (CKiD) Study
Rebecca V Levy, Kimberly J Reidy, Thu H Le, et al.
Yi Chuan = Hereditas
|
July 11, 2006
[Association study of chromosome 4 STRs polymorphisms with nasopharyngeal carcinoma]
Xiu-Chan Guo, Stephen J O'Brien, Cheryl Winkler, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 69) with videos related to
Sort By:
Page
of 7
Investigative Ophthalmology & Visual Science
|
January 8, 2010
Mutation discovered in a feline model of human congenital retinal blinding disease
Marilyn Menotti-Raymond, Koren Holland Deckman, Victor David, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
February 5, 2020
Maternal variants within the apolipoprotein L1 gene are associated with preeclampsia in a South African cohort of African ancestry
Semone Thakoordeen-Reddy, Cheryl Winkler, Jagidesa Moodley, et al.
Veterinary Ophthalmology
|
September 16, 2009
Retinal degeneration in the Abyssinian and Somali cat (rdAc): correlation between genotype and phenotype and rdAc allele frequency in two continents
Kristina Narfström, Victor David, Oswald Jarret, et al.
Frontiers in Molecular Biosciences
|
December 20, 2021
Structure-Function Relationship of the Disintegrin Family: Sequence Signature and Integrin Interaction
Ariana A Vasconcelos, Jorge C Estrada, Victor David, et al.
Zoological Letters
|
February 27, 2025
Potential of Garra rufa as a novel high-temperature resistant model fish: a review on current and future approaches
Yasuhito Shimada, Baki Aydın, Koto Kon-Nanjo, et al.
Scientific Data
|
May 9, 2025
Chromosome-level genome assembly of the doctor fish (Garra rufa)
Tetsuo Kon, Koto Kon-Nanjo, Kiki Syaputri Handayani, et al.
Toxins
|
August 9, 2018
Recombinant and Chimeric Disintegrins in Preclinical Research
Victor David, Barbara Barbosa Succar, João Alfredo de Moraes, et al.
The Journal of Heredity
|
March 13, 2014
Development of MHC-Linked Microsatellite Markers in the Domestic Cat and Their Use to Evaluate MHC Diversity in Domestic Cats, Cheetahs, and Gir Lions
Katrina M Morris, Katherine Kirby, Julia A Beatty, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 6, 2021
Association of GSTM1 Deletion With Progression of CKD in Children: Findings From the Chronic Kidney Disease in Children (CKiD) Study
Rebecca V Levy, Kimberly J Reidy, Thu H Le, et al.
Yi Chuan = Hereditas
|
July 11, 2006
[Association study of chromosome 4 STRs polymorphisms with nasopharyngeal carcinoma]
Xiu-Chan Guo, Stephen J O'Brien, Cheryl Winkler, et al.
Page
of 7