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Genomics|November 1, 1989
Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3M A Musarella, R G Weleber, W H Murphey, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|November 1, 2012
Aging-related geniohyoid muscle atrophy is related to aspiration status in healthy older adultsXin Feng, Tee Todd, Catherine R Lintzenich, et al.
Biopolymers|June 14, 2020
Mass spectrometry studies of the fragmentation patterns and mechanisms of protonated peptoidsJianhua Ren, Yuan Tian, Ekram Hossain, et al.
Cytogenetics and Cell Genetics|January 1, 1995
CEPH consortium map of chromosome 14D W Cox, G D Billingsley, A E Bale, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research GroupR A Ophoff, G M Terwindt, M N Vergouwe, et al.
Tissue Engineering. Part A|January 12, 2021
Implantation of Engineered Axon Tracts to Bridge Spinal Cord Injury Beyond the Glial Scar in RatsPatricia Zadnik Sullivan, Ahmed AlBayar, Justin C Burrell, et al.
ASN Neuro|March 22, 2026
Membrane Molecular Species Remodeling as a Signature of ω-3 Fatty Acid Action in Cultured Neural CellsKyndall R Nicholas, Hennrique Taborda Ribas, Kevin D Browne, et al.
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