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Developmental Biology
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October 5, 2014
Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression
Anita M Quintana, Elizabeth A Geiger, Nate Achilly, et al.
Oral Oncology
|
November 10, 2018
Aurora kinases are a novel therapeutic target for HPV-positive head and neck cancers
Mushfiq H Shaikh, Adi Idris, Newell W Johnson, et al.
BMC Bioinformatics
|
February 6, 2010
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
Xiaowu Gai, Juan C Perin, Kevin Murphy, et al.
Scientific Reports
|
September 24, 2024
Retraction Note: Performance of graphene-zinc oxide nanocomposite coated-glassy carbon electrode in the sensitive determination of para-nitrophenol
Riyaz Ahmad Dar, Gowhar Ahmad Naikoo, Ashwini Kumar Srivastava, et al.
Scientific Reports
|
January 8, 2022
Performance of graphene-zinc oxide nanocomposite coated-glassy carbon electrode in the sensitive determination of para-nitrophenol
Riyaz Ahmad Dar, Gowhar Ahmad Naikoo, Ashwini Kumar Srivastava, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners
|
May 1, 2023
Evaluation of oncology infusion pharmacy practices: A nationwide survey
A M Boyd, C Sue, A Khandoobhai, et al.
HGG Advances
|
January 20, 2022
Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans
Megan Null, Feyza Yilmaz, David Astling, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 12, 2009
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors
Eric M Jackson, Angela J Sievert, Xiaowu Gai, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy
Hung-Chun Yu, Curtis R Coughlin, Elizabeth A Geiger, et al.
BMC Medical Genomics
|
May 18, 2021
Genome-wide copy number variations in a large cohort of bantu African children
Feyza Yilmaz, Megan Null, David Astling, et al.
Page
of 24
Search research articles
Search
Showing results (171-180 of 236) with videos related to
Sort By:
Page
of 24
Developmental Biology
|
October 5, 2014
Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression
Anita M Quintana, Elizabeth A Geiger, Nate Achilly, et al.
Oral Oncology
|
November 10, 2018
Aurora kinases are a novel therapeutic target for HPV-positive head and neck cancers
Mushfiq H Shaikh, Adi Idris, Newell W Johnson, et al.
BMC Bioinformatics
|
February 6, 2010
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
Xiaowu Gai, Juan C Perin, Kevin Murphy, et al.
Scientific Reports
|
September 24, 2024
Retraction Note: Performance of graphene-zinc oxide nanocomposite coated-glassy carbon electrode in the sensitive determination of para-nitrophenol
Riyaz Ahmad Dar, Gowhar Ahmad Naikoo, Ashwini Kumar Srivastava, et al.
Scientific Reports
|
January 8, 2022
Performance of graphene-zinc oxide nanocomposite coated-glassy carbon electrode in the sensitive determination of para-nitrophenol
Riyaz Ahmad Dar, Gowhar Ahmad Naikoo, Ashwini Kumar Srivastava, et al.
Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners
|
May 1, 2023
Evaluation of oncology infusion pharmacy practices: A nationwide survey
A M Boyd, C Sue, A Khandoobhai, et al.
HGG Advances
|
January 20, 2022
Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans
Megan Null, Feyza Yilmaz, David Astling, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 12, 2009
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors
Eric M Jackson, Angela J Sievert, Xiaowu Gai, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy
Hung-Chun Yu, Curtis R Coughlin, Elizabeth A Geiger, et al.
BMC Medical Genomics
|
May 18, 2021
Genome-wide copy number variations in a large cohort of bantu African children
Feyza Yilmaz, Megan Null, David Astling, et al.
Page
of 24