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P Dane Witmer

Showing results (1-10 of 23) with videos related to

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Cancer Biology & Therapy|July 31, 2007
DNA methylation regulates MicroRNA expressionLiangfeng Han, P Dane Witmer, Emily Casey, et al.
The Journal of Biological Chemistry|June 29, 2007
MicroRNA (miRNA) transcriptome of mouse retina and identification of a sensory organ-specific miRNA clusterShunbin Xu, P Dane Witmer, Stephen Lumayag, et al.
Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
Haematologica|March 6, 2016
Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemiaRuijuan Li, Nara Sobreira, P Dane Witmer, et al.
Scientific Reports|July 19, 2020
Spectrum of genetic variants in moderate to severe sporadic hearing loss in PakistanMemoona Ramzan, Rasheeda Bashir, Midhat Salman, et al.
Scientific Reports|June 21, 2024
Identification and analyses of exonic and copy number variants in spastic paraplegiaAnum Shafique, Ayesha Nadeem, Faiza Aslam, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
miRNA mutations are not a common cause of deafnessMichael S Hildebrand, P Dane Witmer, Shunbin Xu, et al.
Cell Genomics|June 27, 2022
Lumping versus splitting: How to approach defining a disease to enable accurate genomic curationCourtney Thaxton, Jennifer Goldstein, Marina DiStefano, et al.
Frontiers in Genetics|June 21, 2024
Rare exonic <i>CELSR3</i> variants identified in Bladder Exstrophy Epispadias ComplexAngie C Jelin, Nikolai Sopko, Nara Sobreira, et al.
Prenatal Diagnosis|January 30, 2020
The utility of exome sequencing for fetal pleural effusionsAngie C Jelin, Nara Sobreira, Elizabeth Wohler, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Cancer Biology & Therapy|July 31, 2007
DNA methylation regulates MicroRNA expressionLiangfeng Han, P Dane Witmer, Emily Casey, et al.
The Journal of Biological Chemistry|June 29, 2007
MicroRNA (miRNA) transcriptome of mouse retina and identification of a sensory organ-specific miRNA clusterShunbin Xu, P Dane Witmer, Stephen Lumayag, et al.
Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
Haematologica|March 6, 2016
Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemiaRuijuan Li, Nara Sobreira, P Dane Witmer, et al.
Scientific Reports|July 19, 2020
Spectrum of genetic variants in moderate to severe sporadic hearing loss in PakistanMemoona Ramzan, Rasheeda Bashir, Midhat Salman, et al.
Scientific Reports|June 21, 2024
Identification and analyses of exonic and copy number variants in spastic paraplegiaAnum Shafique, Ayesha Nadeem, Faiza Aslam, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
miRNA mutations are not a common cause of deafnessMichael S Hildebrand, P Dane Witmer, Shunbin Xu, et al.
Cell Genomics|June 27, 2022
Lumping versus splitting: How to approach defining a disease to enable accurate genomic curationCourtney Thaxton, Jennifer Goldstein, Marina DiStefano, et al.
Frontiers in Genetics|June 21, 2024
Rare exonic <i>CELSR3</i> variants identified in Bladder Exstrophy Epispadias ComplexAngie C Jelin, Nikolai Sopko, Nara Sobreira, et al.
Prenatal Diagnosis|January 30, 2020
The utility of exome sequencing for fetal pleural effusionsAngie C Jelin, Nara Sobreira, Elizabeth Wohler, et al.
Pageof 3