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H Farkas

Showing results (141-150 of 162) with videos related to

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The American Journal of Surgical Pathology|December 19, 2019
"Renal Cell Carcinoma With Leiomyomatous Stroma" Harbor Somatic Mutations of TSC1, TSC2, MTOR, and/or ELOC (TCEB1): Clinicopathologic and Molecular Characterization of 18 Sporadic Tumors Supports a Distinct EntityRajal B Shah, Bradley A Stohr, Zheng Jin Tu, et al.
Investigative Ophthalmology & Visual Science|December 4, 2014
Targeted exon sequencing in Usher syndrome type IKinga M Bujakowska, Mark Consugar, Emily Place, et al.
Allergy|October 12, 2013
Repeat treatment with icatibant for multiple hereditary angioedema attacks: FAST-2 open-label studyM Baş, J Greve, T K Hoffmann, et al.
Clinical Chemistry|October 7, 2017
Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal TestingNilesh G Dharajiya, Daniel S Grosu, Daniel H Farkas, et al.
Investigative Ophthalmology & Visual Science|August 25, 2004
Identification of gene expression changes associated with the progression of retinal degeneration in the rd1 mouseAbigail S Hackam, Richelle Strom, Dongmei Liu, et al.
The Journal of Infectious Diseases|October 10, 2022
Alpha to Omicron: Disease Severity and Clinical Outcomes of Major SARS-CoV-2 VariantsFrank P Esper, Thamali M Adhikari, Zheng Jin Tu, et al.
Investigative Ophthalmology & Visual Science|April 28, 2004
Increased expression of iron-regulating genes in monkey and human glaucomaRonald H Farkas, Itay Chowers, Abigail S Hackam, et al.
JAMA Network Open|April 26, 2021
Genomic Epidemiology of SARS-CoV-2 Infection During the Initial Pandemic Wave and Association With Disease SeverityFrank P Esper, Yu-Wei Cheng, Thamali M Adhikari, et al.
Archives of Pathology & Laboratory Medicine|November 25, 2003
Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutationsSusan H Bernacki, Daniel H Farkas, Wenmei Shi, et al.
Archives of Pathology & Laboratory Medicine|November 4, 2020
Diagnostic Utility of a Custom 34-Gene Anchored Multiplex PCR-Based Next-Generation Sequencing Fusion Panel for the Diagnosis of Bone and Soft Tissue Neoplasms With Identification of Novel USP6 Fusion Partners in Aneurysmal Bone CystsJosephine K Dermawan, Yu Wei Cheng, Zheng Jin Tu, et al.
Pageof 17

Showing results (141-150 of 162) with videos related to

Sort By:
Pageof 17
The American Journal of Surgical Pathology|December 19, 2019
"Renal Cell Carcinoma With Leiomyomatous Stroma" Harbor Somatic Mutations of TSC1, TSC2, MTOR, and/or ELOC (TCEB1): Clinicopathologic and Molecular Characterization of 18 Sporadic Tumors Supports a Distinct EntityRajal B Shah, Bradley A Stohr, Zheng Jin Tu, et al.
Investigative Ophthalmology & Visual Science|December 4, 2014
Targeted exon sequencing in Usher syndrome type IKinga M Bujakowska, Mark Consugar, Emily Place, et al.
Allergy|October 12, 2013
Repeat treatment with icatibant for multiple hereditary angioedema attacks: FAST-2 open-label studyM Baş, J Greve, T K Hoffmann, et al.
Clinical Chemistry|October 7, 2017
Incidental Detection of Maternal Neoplasia in Noninvasive Prenatal TestingNilesh G Dharajiya, Daniel S Grosu, Daniel H Farkas, et al.
Investigative Ophthalmology & Visual Science|August 25, 2004
Identification of gene expression changes associated with the progression of retinal degeneration in the rd1 mouseAbigail S Hackam, Richelle Strom, Dongmei Liu, et al.
The Journal of Infectious Diseases|October 10, 2022
Alpha to Omicron: Disease Severity and Clinical Outcomes of Major SARS-CoV-2 VariantsFrank P Esper, Thamali M Adhikari, Zheng Jin Tu, et al.
Investigative Ophthalmology & Visual Science|April 28, 2004
Increased expression of iron-regulating genes in monkey and human glaucomaRonald H Farkas, Itay Chowers, Abigail S Hackam, et al.
JAMA Network Open|April 26, 2021
Genomic Epidemiology of SARS-CoV-2 Infection During the Initial Pandemic Wave and Association With Disease SeverityFrank P Esper, Yu-Wei Cheng, Thamali M Adhikari, et al.
Archives of Pathology & Laboratory Medicine|November 25, 2003
Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutationsSusan H Bernacki, Daniel H Farkas, Wenmei Shi, et al.
Archives of Pathology & Laboratory Medicine|November 4, 2020
Diagnostic Utility of a Custom 34-Gene Anchored Multiplex PCR-Based Next-Generation Sequencing Fusion Panel for the Diagnosis of Bone and Soft Tissue Neoplasms With Identification of Novel USP6 Fusion Partners in Aneurysmal Bone CystsJosephine K Dermawan, Yu Wei Cheng, Zheng Jin Tu, et al.
Pageof 17