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Showing results (1531-1540 of 2,138) with videos related to
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Plos Genetics
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March 25, 2010
Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform
Pamela R Pretorius, Lisa M Baye, Darryl Y Nishimura, et al.
Human Mutation
|
July 26, 2006
Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His
Michael A Grassi, John H Fingert, Todd E Scheetz, et al.
Investigative Ophthalmology & Visual Science
|
April 27, 2007
IDOCS: intelligent distributed ontology consensus system--the use of machine learning in retinal drusen phenotyping
George Thomas, Michael A Grassi, John R Lee, et al.
Translational Vision Science & Technology
|
December 7, 2018
Correlation of Optical Coherence Tomography and Retinal Histology in Normal and Pro23His Retinal Degeneration Pig
Justine Cheng, Elliott H Sohn, Chunhua Jiao, et al.
Leukemia & Lymphoma
|
February 20, 2016
Clinical impact of ABL1 kinase domain mutations and IKZF1 deletion in adults under age 60 with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL): molecular analysis of CALGB (Alliance) 10001 and 9665
Rebecca DeBoer, Gregory Koval, Flora Mulkey, et al.
MMWR. Morbidity and Mortality Weekly Report
|
January 31, 2020
Syndromic Surveillance of Suicidal Ideation and Self-Directed Violence - United States, January 2017-December 2018
Marissa L Zwald, Kristin M Holland, Francis B Annor, et al.
Journal of the American College of Surgeons
|
March 30, 2020
Impact of Procedure Type, Case Duration, and Adjunctive Equipment on Surgeon Intraoperative Musculoskeletal Discomfort
Liyun Yang, Samuel R Money, Melissa M Morrow, et al.
Experimental Eye Research
|
May 5, 2007
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)
B Bakall, R A Radu, J B Stanton, et al.
Science (New York, N.Y.)
|
February 26, 2000
Virus-induced neuronal apoptosis blocked by the herpes simplex virus latency-associated transcript
G C Perng, C Jones, J Ciacci-Zanella, et al.
Nature Genetics
|
September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndrome
A M Slavotinek, E M Stone, K Mykytyn, et al.
Page
of 214
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Showing results (1531-1540 of 2,138) with videos related to
Sort By:
Page
of 214
Plos Genetics
|
March 25, 2010
Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform
Pamela R Pretorius, Lisa M Baye, Darryl Y Nishimura, et al.
Human Mutation
|
July 26, 2006
Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His
Michael A Grassi, John H Fingert, Todd E Scheetz, et al.
Investigative Ophthalmology & Visual Science
|
April 27, 2007
IDOCS: intelligent distributed ontology consensus system--the use of machine learning in retinal drusen phenotyping
George Thomas, Michael A Grassi, John R Lee, et al.
Translational Vision Science & Technology
|
December 7, 2018
Correlation of Optical Coherence Tomography and Retinal Histology in Normal and Pro23His Retinal Degeneration Pig
Justine Cheng, Elliott H Sohn, Chunhua Jiao, et al.
Leukemia & Lymphoma
|
February 20, 2016
Clinical impact of ABL1 kinase domain mutations and IKZF1 deletion in adults under age 60 with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL): molecular analysis of CALGB (Alliance) 10001 and 9665
Rebecca DeBoer, Gregory Koval, Flora Mulkey, et al.
MMWR. Morbidity and Mortality Weekly Report
|
January 31, 2020
Syndromic Surveillance of Suicidal Ideation and Self-Directed Violence - United States, January 2017-December 2018
Marissa L Zwald, Kristin M Holland, Francis B Annor, et al.
Journal of the American College of Surgeons
|
March 30, 2020
Impact of Procedure Type, Case Duration, and Adjunctive Equipment on Surgeon Intraoperative Musculoskeletal Discomfort
Liyun Yang, Samuel R Money, Melissa M Morrow, et al.
Experimental Eye Research
|
May 5, 2007
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)
B Bakall, R A Radu, J B Stanton, et al.
Science (New York, N.Y.)
|
February 26, 2000
Virus-induced neuronal apoptosis blocked by the herpes simplex virus latency-associated transcript
G C Perng, C Jones, J Ciacci-Zanella, et al.
Nature Genetics
|
September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndrome
A M Slavotinek, E M Stone, K Mykytyn, et al.
Page
of 214