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Katia Sol-Church

Showing results (51-60 of 68) with videos related to

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Molecular Human Reproduction|October 28, 2015
Polygenic inheritance of cryptorchidism susceptibility in the LE/orl ratJulia Spencer Barthold, Joan Pugarelli, Madolyn L MacDonald, et al.
American Journal of Medical Genetics. Part A|November 15, 2014
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndromeKaren W Gripp, Katherine M Robbins, Nara L Sobreira, et al.
Molecular Genetics & Genomic Medicine|August 7, 2015
SMN1 and SMN2 copy numbers in cell lines derived from patients with spinal muscular atrophy as measured by array digital PCRDeborah L Stabley, Ashlee W Harris, Jennifer Holbrook, et al.
American Journal of Medical Genetics. Part A|June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndromeKaren W Gripp, Angela E Lin, Linda Nicholson, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlationKaren W Gripp, Angela E Lin, Deborah L Stabley, et al.
Circulation. Arrhythmia and Electrophysiology|February 28, 2024
<i>HRAS</i>-Mutant Cardiomyocyte Model of Multifocal Atrial TachycardiaNelson A Rodríguez, Nihir Patel, Rafael Dariolli, et al.
Nature Communications|January 22, 2025
Microglia modulate the cerebrovascular reactivity through ectonucleotidase CD39Zhongxiao Fu, Mallikarjunarao Ganesana, Philip Hwang, et al.
American Journal of Medical Genetics. Part A|March 26, 2011
Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13CKaren W Gripp, Elizabeth Hopkins, Katia Sol-Church, et al.
Iscience|February 2, 2024
Nanosphere pharmacodynamics improves safety of immunostimulatory cytokine therapyRyan A Lacinski, Sebastian A Dziadowicz, Amanda Stewart, et al.
BMC Urology|October 23, 2016
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidismYanping Wang, Jin Li, Thomas F Kolon, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Molecular Human Reproduction|October 28, 2015
Polygenic inheritance of cryptorchidism susceptibility in the LE/orl ratJulia Spencer Barthold, Joan Pugarelli, Madolyn L MacDonald, et al.
American Journal of Medical Genetics. Part A|November 15, 2014
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndromeKaren W Gripp, Katherine M Robbins, Nara L Sobreira, et al.
Molecular Genetics & Genomic Medicine|August 7, 2015
SMN1 and SMN2 copy numbers in cell lines derived from patients with spinal muscular atrophy as measured by array digital PCRDeborah L Stabley, Ashlee W Harris, Jennifer Holbrook, et al.
American Journal of Medical Genetics. Part A|June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndromeKaren W Gripp, Angela E Lin, Linda Nicholson, et al.
American Journal of Medical Genetics. Part A|December 6, 2005
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlationKaren W Gripp, Angela E Lin, Deborah L Stabley, et al.
Circulation. Arrhythmia and Electrophysiology|February 28, 2024
<i>HRAS</i>-Mutant Cardiomyocyte Model of Multifocal Atrial TachycardiaNelson A Rodríguez, Nihir Patel, Rafael Dariolli, et al.
Nature Communications|January 22, 2025
Microglia modulate the cerebrovascular reactivity through ectonucleotidase CD39Zhongxiao Fu, Mallikarjunarao Ganesana, Philip Hwang, et al.
American Journal of Medical Genetics. Part A|March 26, 2011
Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13CKaren W Gripp, Elizabeth Hopkins, Katia Sol-Church, et al.
Iscience|February 2, 2024
Nanosphere pharmacodynamics improves safety of immunostimulatory cytokine therapyRyan A Lacinski, Sebastian A Dziadowicz, Amanda Stewart, et al.
BMC Urology|October 23, 2016
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidismYanping Wang, Jin Li, Thomas F Kolon, et al.
Pageof 7