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American Journal of Human Genetics|May 13, 2004
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndromeMelissa A Parisi, Craig L Bennett, Melissa L Eckert, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
Engineered human lymph node stroma model for examining interstitial fluid flow and T cell egressJennifer H Hammel, Abhinav Arneja, Jessica Cunningham, et al.
Journal of Nuclear Medicine Technology|December 22, 2021
Global and Regional Variations in Transthyretin Cardiac Amyloidosis: A Comparison of Longitudinal Strain and 99mTc-Pyrophosphate ImagingChristopher Lee, Chieh-Ju Chao, Pradyumna Agasthi, et al.
Injury|August 5, 2022
A multicenter evaluation on the impact of non-therapeutic transfer in rural traumaJames M Bardes, Daniel J Grabo, Aimee LaRiccia, et al.
Protein Engineering|September 1, 1992
Altering the association properties of insulin by amino acid replacementD N Brems, L A Alter, M J Beckage, et al.
Biosensors & Bioelectronics|October 19, 2005
Fabricating optical fiber imaging sensors using ink jet printing technology: a pH sensor proof-of-conceptJ Chance Carter, Rosa M Alvis, Steve B Brown, et al.
Mycologia|February 16, 2024
Three new species in Russula subsection Xerampelinae supported by genealogical and phenotypic coherenceChance R Noffsinger, Katarína Adamčíková, Ursula Eberhardt, et al.
Human Genetics|November 1, 1991
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.
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