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Showing results (431-440 of 688) with videos related to

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The American Journal of Pathology|July 24, 2003
Identification of genes up-regulated in urothelial tumors: the 67-kd laminin receptor and tumor-associated trypsin inhibitorChristine P Diggle, Sheena Cruickshank, Jonathon D Olsburgh, et al.
American Journal of Physical Anthropology|July 17, 1999
Developmental components of resting ventilation among high- and low-altitude Andean children and adultsA R Frisancho, P C Juliao, V Barcelona, et al.
Genes, Chromosomes & Cancer|March 29, 2002
Molecular genetic analysis of chromosome 9 candidate tumor-suppressor loci in bladder cancer cell linesSarah V Williams, Kathryn D Sibley, Alison M Davies, et al.
Journal of Medicinal Chemistry|November 15, 2021
From Fragment to Lead: De Novo Design and Development toward a Selective FGFR2 InhibitorLewis D Turner, Chi H Trinh, Ryan A Hubball, et al.
American Journal of Human Genetics|September 6, 2014
Transcriptome sequencing of a large human family identifies the impact of rare noncoding variantsXin Li, Alexis Battle, Konrad J Karczewski, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993D J Kwiatkowski, J Armour, A E Bale, et al.
Genes, Chromosomes & Cancer|May 13, 2010
High-resolution analysis of genomic alteration on chromosome arm 8p in urothelial carcinomaSarah V Williams, Fiona M Platt, Carolyn D Hurst, et al.
Human Biology|May 24, 2006
Applications of pooled DNA samples to the assessment of population affinities: short tandem repeatsM H Crawford, P Banerjee, D A Demarchi, et al.
Scientific Reports|February 4, 2018
Dlgap1 knockout mice exhibit alterations of the postsynaptic density and selective reductions in sociabilityM P Coba, M J Ramaker, E V Ho, et al.
Molecular Genetics & Genomic Medicine|October 10, 2019
A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing lossElina Kari, Lorida Llaci, John L Go, et al.
Pageof 69

Showing results (431-440 of 688) with videos related to

Sort By:
Pageof 69
The American Journal of Pathology|July 24, 2003
Identification of genes up-regulated in urothelial tumors: the 67-kd laminin receptor and tumor-associated trypsin inhibitorChristine P Diggle, Sheena Cruickshank, Jonathon D Olsburgh, et al.
American Journal of Physical Anthropology|July 17, 1999
Developmental components of resting ventilation among high- and low-altitude Andean children and adultsA R Frisancho, P C Juliao, V Barcelona, et al.
Genes, Chromosomes & Cancer|March 29, 2002
Molecular genetic analysis of chromosome 9 candidate tumor-suppressor loci in bladder cancer cell linesSarah V Williams, Kathryn D Sibley, Alison M Davies, et al.
Journal of Medicinal Chemistry|November 15, 2021
From Fragment to Lead: De Novo Design and Development toward a Selective FGFR2 InhibitorLewis D Turner, Chi H Trinh, Ryan A Hubball, et al.
American Journal of Human Genetics|September 6, 2014
Transcriptome sequencing of a large human family identifies the impact of rare noncoding variantsXin Li, Alexis Battle, Konrad J Karczewski, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993D J Kwiatkowski, J Armour, A E Bale, et al.
Genes, Chromosomes & Cancer|May 13, 2010
High-resolution analysis of genomic alteration on chromosome arm 8p in urothelial carcinomaSarah V Williams, Fiona M Platt, Carolyn D Hurst, et al.
Human Biology|May 24, 2006
Applications of pooled DNA samples to the assessment of population affinities: short tandem repeatsM H Crawford, P Banerjee, D A Demarchi, et al.
Scientific Reports|February 4, 2018
Dlgap1 knockout mice exhibit alterations of the postsynaptic density and selective reductions in sociabilityM P Coba, M J Ramaker, E V Ho, et al.
Molecular Genetics & Genomic Medicine|October 10, 2019
A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing lossElina Kari, Lorida Llaci, John L Go, et al.
Pageof 69