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BMC Medical Genomics
|
February 12, 2024
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review
Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Aysan Moeinafshar, et al.
BMC Medical Genomics
|
August 5, 2024
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Mohammad-Reza Ghasemi, Hossein Sadeghi, Farzad Hashemi-Gorji, et al.
Oncotarget
|
April 28, 2016
Over-expression of the miR-483-3p overcomes the miR-145/TP53 pro-apoptotic loop in hepatocellular carcinoma
Laura Lupini, Felice Pepe, Manuela Ferracin, et al.
Oncoimmunology
|
January 27, 2017
Deficiency of the adaptor protein SLy1 results in a natural killer cell ribosomopathy affecting tumor clearance
Saeed Arefanian, Daniel Schäll, Stephanie Chang, et al.
Scientific Reports
|
June 25, 2017
Dacomitinib, a pan-inhibitor of ErbB receptors, suppresses growth and invasive capacity of chemoresistant ovarian carcinoma cells
Majid Momeny, Ghazaleh Zarrinrad, Farima Moghaddaskho, et al.
European Journal of Human Genetics : EJHG
|
January 26, 2024
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies
Parisa Vaseghi, Laleh Habibi, Julie A Neidich, et al.
American Journal of Medical Genetics. Part A
|
December 21, 2024
Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)
Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Afif Ben-Mahmoud, et al.
Genome Medicine
|
October 25, 2025
Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes
Yingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 8, 2025
Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes
Yingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
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Showing results (131-140 of 139) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 139 results.
BMC Medical Genomics
|
February 12, 2024
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review
Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Aysan Moeinafshar, et al.
BMC Medical Genomics
|
August 5, 2024
Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism
Mohammad-Reza Ghasemi, Hossein Sadeghi, Farzad Hashemi-Gorji, et al.
Oncotarget
|
April 28, 2016
Over-expression of the miR-483-3p overcomes the miR-145/TP53 pro-apoptotic loop in hepatocellular carcinoma
Laura Lupini, Felice Pepe, Manuela Ferracin, et al.
Oncoimmunology
|
January 27, 2017
Deficiency of the adaptor protein SLy1 results in a natural killer cell ribosomopathy affecting tumor clearance
Saeed Arefanian, Daniel Schäll, Stephanie Chang, et al.
Scientific Reports
|
June 25, 2017
Dacomitinib, a pan-inhibitor of ErbB receptors, suppresses growth and invasive capacity of chemoresistant ovarian carcinoma cells
Majid Momeny, Ghazaleh Zarrinrad, Farima Moghaddaskho, et al.
European Journal of Human Genetics : EJHG
|
January 26, 2024
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies
Parisa Vaseghi, Laleh Habibi, Julie A Neidich, et al.
American Journal of Medical Genetics. Part A
|
December 21, 2024
Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)
Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Afif Ben-Mahmoud, et al.
Genome Medicine
|
October 25, 2025
Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes
Yingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 8, 2025
Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes
Yingxi Wang, Eleanor I Sams, Rachel Slaugh, et al.
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of 14