Search research articles
Contact Us
Filters
Showing results (431-440 of 688) with videos related to
Page
of 69
Sort By:
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 inhibitor
Christine 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 adults
A 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 lines
Sarah 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 Inhibitor
Lewis 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 variants
Xin 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 1993
D 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 carcinoma
Sarah 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 repeats
M 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 sociability
M 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 loss
Elina Kari, Lorida Llaci, John L Go, et al.
Page
of 69
Search research articles
Search
Showing results (431-440 of 688) with videos related to
Sort By:
Page
of 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 inhibitor
Christine 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 adults
A 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 lines
Sarah 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 Inhibitor
Lewis 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 variants
Xin 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 1993
D 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 carcinoma
Sarah 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 repeats
M 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 sociability
M 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 loss
Elina Kari, Lorida Llaci, John L Go, et al.
Page
of 69