Search research articles
Contact Us
Filters
Showing results (361-370 of 377) with videos related to
Page
of 38
Sort By:
Oncotarget
|
November 4, 2015
IRAK1 is a novel DEK transcriptional target and is essential for head and neck cancer cell survival
Allie K Adams, Lyndsey C Bolanos, Phillip J Dexheimer, et al.
Clinical Genetics
|
January 25, 2014
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome
S Lohan, M Spielmann, S C Doelken, et al.
Oncogene
|
March 11, 2014
DEK promotes HPV-positive and -negative head and neck cancer cell proliferation
A K Adams, G E Hallenbeck, K A Casper, et al.
Journal of the American Heart Association
|
April 7, 2026
Factors Influencing Quality Improvement Success in Primary Care: A Comparative Case Study of High- and Low-Performing Sites in Patient Hypertension Outcomes
Jacqueline M Knapke, Manpreet Kaur, Sonal J Patil, et al.
Scientific Reports
|
January 13, 2021
Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing
Shalini S Nayak, Pauline E Schneeberger, Siddaramappa J Patil, et al.
Journal Francais D'Ophtalmologie
|
December 16, 2019
MIIRetCam (Make In India Retina Camera) assisted retinal imaging in paediatric patients: Useful, artefacts, learning curve
A Sharma, Y Bilong, J Patil, et al.
American Journal of Medical Genetics. Part A
|
June 25, 2016
Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease
Prajnya Ranganath, Divya Matta, Gandham SriLakshmi Bhavani, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2024
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, et al.
Brain : a Journal of Neurology
|
September 18, 2024
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects
Elizabeth A Werren, Guillermo Rodriguez Bey, Purvi Majethia, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2024
Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia
Prince Jacob, Swati Singh, Gandham SriLakshmi Bhavani, et al.
Page
of 38
Search research articles
Search
Showing results (361-370 of 377) with videos related to
Sort By:
Page
of 38
Oncotarget
|
November 4, 2015
IRAK1 is a novel DEK transcriptional target and is essential for head and neck cancer cell survival
Allie K Adams, Lyndsey C Bolanos, Phillip J Dexheimer, et al.
Clinical Genetics
|
January 25, 2014
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome
S Lohan, M Spielmann, S C Doelken, et al.
Oncogene
|
March 11, 2014
DEK promotes HPV-positive and -negative head and neck cancer cell proliferation
A K Adams, G E Hallenbeck, K A Casper, et al.
Journal of the American Heart Association
|
April 7, 2026
Factors Influencing Quality Improvement Success in Primary Care: A Comparative Case Study of High- and Low-Performing Sites in Patient Hypertension Outcomes
Jacqueline M Knapke, Manpreet Kaur, Sonal J Patil, et al.
Scientific Reports
|
January 13, 2021
Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing
Shalini S Nayak, Pauline E Schneeberger, Siddaramappa J Patil, et al.
Journal Francais D'Ophtalmologie
|
December 16, 2019
MIIRetCam (Make In India Retina Camera) assisted retinal imaging in paediatric patients: Useful, artefacts, learning curve
A Sharma, Y Bilong, J Patil, et al.
American Journal of Medical Genetics. Part A
|
June 25, 2016
Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease
Prajnya Ranganath, Divya Matta, Gandham SriLakshmi Bhavani, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2024
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia, et al.
Brain : a Journal of Neurology
|
September 18, 2024
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects
Elizabeth A Werren, Guillermo Rodriguez Bey, Purvi Majethia, et al.
European Journal of Human Genetics : EJHG
|
December 20, 2024
Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia
Prince Jacob, Swati Singh, Gandham SriLakshmi Bhavani, et al.
Page
of 38