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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
January 17, 2025
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant Inheritance
Aline L Petrin, Ligiane Alves Machado-Paula, Austin Hinkle, et al.
American Journal of Human Genetics
|
May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
James O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
The Journal of Pediatrics
|
January 18, 2013
Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births
Nansi S Boghossian, Grier P Page, Edward F Bell, et al.
Nature Genetics
|
September 6, 2000
Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease
A Kinoshita, T Saito, H Tomita, et al.
American Journal of Medical Genetics. Part A
|
May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome
Nicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
Scientific Reports
|
October 15, 2022
Pericytes take up and degrade α-synuclein but succumb to apoptosis under cellular stress
Taylor J Stevenson, Rebecca H Johnson, Jimmy Savistchenko, et al.
The Lancet. Infectious Diseases
|
September 3, 2022
The Johns Hopkins University Center for Systems Science and Engineering COVID-19 Dashboard: data collection process, challenges faced, and lessons learned
Ensheng Dong, Jeremy Ratcliff, Tamara D Goyea, et al.
BMC Public Health
|
February 16, 2024
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research
Abimbola M Oladayo, Oluwakemi Odukoya, Veronica Sule, et al.
Nature Medicine
|
June 1, 2010
Recovery of motoneuron and locomotor function after spinal cord injury depends on constitutive activity in 5-HT2C receptors
Katherine C Murray, Aya Nakae, Marilee J Stephens, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
April 18, 2021
Randomized Trial of the Efficacy and Safety of Berotralstat (BCX7353) as an Oral Prophylactic Therapy for Hereditary Angioedema: Results of APeX-2 Through 48 Weeks (Part 2)
H James Wedner, Emel Aygören-Pürsün, Jonathan Bernstein, et al.
Page
of 147
Search research articles
Search
Showing results (1251-1260 of 1,465) with videos related to
Sort By:
Page
of 147
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
January 17, 2025
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant Inheritance
Aline L Petrin, Ligiane Alves Machado-Paula, Austin Hinkle, et al.
American Journal of Human Genetics
|
May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
James O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
The Journal of Pediatrics
|
January 18, 2013
Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births
Nansi S Boghossian, Grier P Page, Edward F Bell, et al.
Nature Genetics
|
September 6, 2000
Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease
A Kinoshita, T Saito, H Tomita, et al.
American Journal of Medical Genetics. Part A
|
May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome
Nicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
Scientific Reports
|
October 15, 2022
Pericytes take up and degrade α-synuclein but succumb to apoptosis under cellular stress
Taylor J Stevenson, Rebecca H Johnson, Jimmy Savistchenko, et al.
The Lancet. Infectious Diseases
|
September 3, 2022
The Johns Hopkins University Center for Systems Science and Engineering COVID-19 Dashboard: data collection process, challenges faced, and lessons learned
Ensheng Dong, Jeremy Ratcliff, Tamara D Goyea, et al.
BMC Public Health
|
February 16, 2024
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research
Abimbola M Oladayo, Oluwakemi Odukoya, Veronica Sule, et al.
Nature Medicine
|
June 1, 2010
Recovery of motoneuron and locomotor function after spinal cord injury depends on constitutive activity in 5-HT2C receptors
Katherine C Murray, Aya Nakae, Marilee J Stephens, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
April 18, 2021
Randomized Trial of the Efficacy and Safety of Berotralstat (BCX7353) as an Oral Prophylactic Therapy for Hereditary Angioedema: Results of APeX-2 Through 48 Weeks (Part 2)
H James Wedner, Emel Aygören-Pürsün, Jonathan Bernstein, et al.
Page
of 147