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A Grebe

Showing results (11-20 of 44) with videos related to

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Journal of Clinical and Experimental Neuropsychology|October 18, 2024
Cognitive reserve in individuals with frontotemporal dementia: a systematic reviewLauren A Grebe, Jet M J Vonk, Elizabeth E Galletta, et al.
Molecular and Cellular Biology|February 25, 2000
Acetyl coenzyme A stimulates RNA polymerase II transcription and promoter binding by transcription factor IID in the absence of histonesS K Galasinski, T N Lively, A Grebe De Barron, et al.
American Journal of Medical Genetics. Part A|February 11, 2021
A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocationBeate Peter, Nancy Scherer, Winnie S Liang, et al.
American Journal of Medical Genetics|August 1, 1993
Further delineation of the epidermal nevus syndrome: two cases with new findings and literature reviewT A Grebe, M E Rimsza, S F Richter, et al.
Life (Basel, Switzerland)|June 26, 2026
Chromosomal Microarray Analysis in Critically Ill Neonates and Children: Diagnostic Yield and Clinical UtilityJoshua Meyer, Emily Hershman, Ananditha Sivakumaran, et al.
Blood|July 15, 1995
A conserved TATA-less proximal promoter drives basal transcription from the urokinase-type plasminogen activator receptor geneE Soravia, A Grebe, P De Luca, et al.
Pediatrics|February 22, 2012
Prevalence of autism spectrum disorders in Hispanic and non-Hispanic white childrenAnita Pedersen, Sydney Pettygrove, F John Meaney, et al.
Genetics in Medicine Open|October 13, 2025
Clinical utility of runs of homozygosity in the identification of genetic causes in individuals with rare diseasesTheru A Sivakumaran, Bilal Azab, Emily Hershman, et al.
Pediatric Dermatology|January 22, 2025
Granulomatous Variant of Giant Centrifugal Miliaria Profunda in an 8-Month-Old Boy: Expanding the Dermatologic Phenotype of Cardiofaciocutaneous SyndromeHannah C Tolson, Fatmah Alzahrani, Raj Singh, et al.
Biochemical and Biophysical Research Communications|October 26, 1999
Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiencyG He, B Z Yang, D S Roe, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Journal of Clinical and Experimental Neuropsychology|October 18, 2024
Cognitive reserve in individuals with frontotemporal dementia: a systematic reviewLauren A Grebe, Jet M J Vonk, Elizabeth E Galletta, et al.
Molecular and Cellular Biology|February 25, 2000
Acetyl coenzyme A stimulates RNA polymerase II transcription and promoter binding by transcription factor IID in the absence of histonesS K Galasinski, T N Lively, A Grebe De Barron, et al.
American Journal of Medical Genetics. Part A|February 11, 2021
A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocationBeate Peter, Nancy Scherer, Winnie S Liang, et al.
American Journal of Medical Genetics|August 1, 1993
Further delineation of the epidermal nevus syndrome: two cases with new findings and literature reviewT A Grebe, M E Rimsza, S F Richter, et al.
Life (Basel, Switzerland)|June 26, 2026
Chromosomal Microarray Analysis in Critically Ill Neonates and Children: Diagnostic Yield and Clinical UtilityJoshua Meyer, Emily Hershman, Ananditha Sivakumaran, et al.
Blood|July 15, 1995
A conserved TATA-less proximal promoter drives basal transcription from the urokinase-type plasminogen activator receptor geneE Soravia, A Grebe, P De Luca, et al.
Pediatrics|February 22, 2012
Prevalence of autism spectrum disorders in Hispanic and non-Hispanic white childrenAnita Pedersen, Sydney Pettygrove, F John Meaney, et al.
Genetics in Medicine Open|October 13, 2025
Clinical utility of runs of homozygosity in the identification of genetic causes in individuals with rare diseasesTheru A Sivakumaran, Bilal Azab, Emily Hershman, et al.
Pediatric Dermatology|January 22, 2025
Granulomatous Variant of Giant Centrifugal Miliaria Profunda in an 8-Month-Old Boy: Expanding the Dermatologic Phenotype of Cardiofaciocutaneous SyndromeHannah C Tolson, Fatmah Alzahrani, Raj Singh, et al.
Biochemical and Biophysical Research Communications|October 26, 1999
Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiencyG He, B Z Yang, D S Roe, et al.
Pageof 5