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Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 2014
Neutral genomic regions refine models of recent rapid human population growth
Elodie Gazave, Li Ma, Diana Chang, et al.
Life Sciences
|
October 10, 2020
NF-κB and STAT3 co-operation enhances high glucose induced aggressiveness of cholangiocarcinoma cells
Charupong Saengboonmee, Chatchai Phoomak, Suangson Supabphol, et al.
Science (New York, N.Y.)
|
April 9, 1993
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy
Y H Fu, D L Friedman, S Richards, et al.
The Journal of Pediatrics
|
November 5, 2020
Loop Diuretics in Severe Bronchopulmonary Dysplasia: Cumulative Use and Associations with Mortality and Age at Discharge
Nicolas A Bamat, Timothy D Nelin, Eric C Eichenwald, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
June 8, 2022
Factors associated with discontinuation of pulmonary vasodilator therapy in children with bronchopulmonary dysplasia-associated pulmonary hypertension
Catherine M Avitabile, Xuemei Zhang, Steve B Ampah, et al.
Genome Research
|
December 19, 2009
A SNP discovery method to assess variant allele probability from next-generation resequencing data
Yufeng Shen, Zhengzheng Wan, Cristian Coarfa, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
May 2, 2025
Pulmonary vasodilator use in very preterm infants in United States children's hospitals
Tomas F Vega, Matthew Huber, Erik A Jensen, et al.
Pediatric Blood & Cancer
|
December 21, 2012
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing
Bradford C Powell, Lichun Jiang, Donna M Muzny, et al.
Molecular Genetics and Metabolism
|
September 26, 2018
Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical gene panels versus genome-wide approaches to molecular diagnosis
Jaya Punetha, Loren Mackay-Loder, Tamar Harel, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria
David R Murdock, Gary D Clark, Matthew N Bainbridge, et al.
Page
of 117
Search research articles
Search
Showing results (591-600 of 1,165) with videos related to
Sort By:
Page
of 117
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 2014
Neutral genomic regions refine models of recent rapid human population growth
Elodie Gazave, Li Ma, Diana Chang, et al.
Life Sciences
|
October 10, 2020
NF-κB and STAT3 co-operation enhances high glucose induced aggressiveness of cholangiocarcinoma cells
Charupong Saengboonmee, Chatchai Phoomak, Suangson Supabphol, et al.
Science (New York, N.Y.)
|
April 9, 1993
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy
Y H Fu, D L Friedman, S Richards, et al.
The Journal of Pediatrics
|
November 5, 2020
Loop Diuretics in Severe Bronchopulmonary Dysplasia: Cumulative Use and Associations with Mortality and Age at Discharge
Nicolas A Bamat, Timothy D Nelin, Eric C Eichenwald, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
June 8, 2022
Factors associated with discontinuation of pulmonary vasodilator therapy in children with bronchopulmonary dysplasia-associated pulmonary hypertension
Catherine M Avitabile, Xuemei Zhang, Steve B Ampah, et al.
Genome Research
|
December 19, 2009
A SNP discovery method to assess variant allele probability from next-generation resequencing data
Yufeng Shen, Zhengzheng Wan, Cristian Coarfa, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
May 2, 2025
Pulmonary vasodilator use in very preterm infants in United States children's hospitals
Tomas F Vega, Matthew Huber, Erik A Jensen, et al.
Pediatric Blood & Cancer
|
December 21, 2012
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing
Bradford C Powell, Lichun Jiang, Donna M Muzny, et al.
Molecular Genetics and Metabolism
|
September 26, 2018
Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical gene panels versus genome-wide approaches to molecular diagnosis
Jaya Punetha, Loren Mackay-Loder, Tamar Harel, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria
David R Murdock, Gary D Clark, Matthew N Bainbridge, et al.
Page
of 117