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Neurogenetics

Showing results (821-830 of 949) with videos related to

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Neurogenetics|January 11, 2007
The medial and lateral substantia nigra in Parkinson's disease: mRNA profiles associated with higher brain tissue vulnerabilityD C Duke, L B Moran, R K B Pearce, et al.
Neurogenetics|August 9, 2005
Differential expression of splice variant and wild-type parkin in sporadic Parkinson's diseaseE K Tan, H Shen, J M M Tan, et al.
Neurogenetics|January 12, 2007
Nf1 expression is dependent on strain background: implications for tumor suppressor haploinsufficiency studiesJessica J Hawes, Robert G Tuskan, Karlyne M Reilly
Neurogenetics|May 23, 2007
Identification of the porcine homologous of human disease causing trinucleotide repeat sequencesLone Bruhn Madsen, Bo Thomsen, Christina Ane Elisabeth Sølvsten, et al.
Neurogenetics|October 13, 2006
A novel deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like diseaseLeonardo Salviati, Eva Trevisson, Maria Cristina Baldoin, et al.
Neurogenetics|May 5, 2006
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM geneAsma Gul, Muhammad Jawad Hassan, Saqib Mahmood, et al.
Neurogenetics|November 26, 2022
Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patientsMiral M Refeat, Walaa El Naggar, Mostafa M El Saied, et al.
Neurogenetics|November 29, 2022
Delineating the phenotype and genetic basis of AMPD2-related pontocerebellar hypoplasiaTal Gilboa, Naama Elefant, Vardiella Meiner, et al.
Neurogenetics|November 20, 2019
Childhood-onset autosomal recessive ataxias: a cross-sectional study from TurkeyHatice Mutlu-Albayrak, Emre Kırat, Gürkan Gürbüz
Neurogenetics|November 2, 2019
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotypeAyşe Candayan, Gulshan Yunisova, Arman Çakar, et al.
Pageof 95

Showing results (821-830 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|January 11, 2007
The medial and lateral substantia nigra in Parkinson's disease: mRNA profiles associated with higher brain tissue vulnerabilityD C Duke, L B Moran, R K B Pearce, et al.
Neurogenetics|August 9, 2005
Differential expression of splice variant and wild-type parkin in sporadic Parkinson's diseaseE K Tan, H Shen, J M M Tan, et al.
Neurogenetics|January 12, 2007
Nf1 expression is dependent on strain background: implications for tumor suppressor haploinsufficiency studiesJessica J Hawes, Robert G Tuskan, Karlyne M Reilly
Neurogenetics|May 23, 2007
Identification of the porcine homologous of human disease causing trinucleotide repeat sequencesLone Bruhn Madsen, Bo Thomsen, Christina Ane Elisabeth Sølvsten, et al.
Neurogenetics|October 13, 2006
A novel deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like diseaseLeonardo Salviati, Eva Trevisson, Maria Cristina Baldoin, et al.
Neurogenetics|May 5, 2006
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM geneAsma Gul, Muhammad Jawad Hassan, Saqib Mahmood, et al.
Neurogenetics|November 26, 2022
Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patientsMiral M Refeat, Walaa El Naggar, Mostafa M El Saied, et al.
Neurogenetics|November 29, 2022
Delineating the phenotype and genetic basis of AMPD2-related pontocerebellar hypoplasiaTal Gilboa, Naama Elefant, Vardiella Meiner, et al.
Neurogenetics|November 20, 2019
Childhood-onset autosomal recessive ataxias: a cross-sectional study from TurkeyHatice Mutlu-Albayrak, Emre Kırat, Gürkan Gürbüz
Neurogenetics|November 2, 2019
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotypeAyşe Candayan, Gulshan Yunisova, Arman Çakar, et al.
Pageof 95