Search research articles
Contact Us
Filters
Showing results (871-880 of 934) with videos related to
Page
of 94
Sort By:
Journal of Alzheimer'S Disease : JAD
|
March 7, 2022
Mitochondrial Targeting of Amyloid-β Protein Precursor Intracellular Domain Induces Hippocampal Cell Death via a Mechanism Distinct from Amyloid-β
Alexandra A Sandberg, Evan Manning, Heather M Wilkins, et al.
Cancer Genetics and Cytogenetics
|
October 1, 1992
Cytogenetic and molecular studies of a familial renal cell carcinoma
H J Decker, B Wullich, J M Whaley, et al.
Ultrasound Quarterly
|
March 15, 2019
Sonographic Diagnosis of Velamentous and Marginal Placental Cord Insertion
Brendan P Kelley, Chad L Klochko, Sarah Atkinson, et al.
American Journal of Medical Genetics
|
August 8, 1997
Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection
Z Chen, T A Grebe, X Y Guan, et al.
Cancer
|
October 15, 1994
Cytogenetic findings in 19 malignant bone tumors
Y Y Ozisik, A M Meloni, A Peier, et al.
Cancer Genetics and Cytogenetics
|
October 1, 1984
Convention on nomenclature for DNA cytometry. Committee on Nomenclature, Society for Analytical Cytology
W Hiddemann, J Schumann, M Andreef, et al.
Investigative Ophthalmology & Visual Science
|
August 31, 2001
Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1)
E L Berson, J L Grimsby, S M Adams, et al.
Human Molecular Genetics
|
March 8, 2007
Mpp4 is required for proper localization of plasma membrane calcium ATPases and maintenance of calcium homeostasis at the rod photoreceptor synaptic terminals
Jun Yang, Basil Pawlyk, Xiao-Hong Wen, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1993
Chromosome instability and the FAMMM syndrome
H T Lynch, R M Fusaro, A A Sandberg, et al.
The New England Journal of Medicine
|
November 8, 1990
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
T P Dryja, T L McGee, L B Hahn, et al.
Page
of 94
Search research articles
Search
Showing results (871-880 of 934) with videos related to
Sort By:
Page
of 94
Journal of Alzheimer'S Disease : JAD
|
March 7, 2022
Mitochondrial Targeting of Amyloid-β Protein Precursor Intracellular Domain Induces Hippocampal Cell Death via a Mechanism Distinct from Amyloid-β
Alexandra A Sandberg, Evan Manning, Heather M Wilkins, et al.
Cancer Genetics and Cytogenetics
|
October 1, 1992
Cytogenetic and molecular studies of a familial renal cell carcinoma
H J Decker, B Wullich, J M Whaley, et al.
Ultrasound Quarterly
|
March 15, 2019
Sonographic Diagnosis of Velamentous and Marginal Placental Cord Insertion
Brendan P Kelley, Chad L Klochko, Sarah Atkinson, et al.
American Journal of Medical Genetics
|
August 8, 1997
Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection
Z Chen, T A Grebe, X Y Guan, et al.
Cancer
|
October 15, 1994
Cytogenetic findings in 19 malignant bone tumors
Y Y Ozisik, A M Meloni, A Peier, et al.
Cancer Genetics and Cytogenetics
|
October 1, 1984
Convention on nomenclature for DNA cytometry. Committee on Nomenclature, Society for Analytical Cytology
W Hiddemann, J Schumann, M Andreef, et al.
Investigative Ophthalmology & Visual Science
|
August 31, 2001
Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1)
E L Berson, J L Grimsby, S M Adams, et al.
Human Molecular Genetics
|
March 8, 2007
Mpp4 is required for proper localization of plasma membrane calcium ATPases and maintenance of calcium homeostasis at the rod photoreceptor synaptic terminals
Jun Yang, Basil Pawlyk, Xiao-Hong Wen, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1993
Chromosome instability and the FAMMM syndrome
H T Lynch, R M Fusaro, A A Sandberg, et al.
The New England Journal of Medicine
|
November 8, 1990
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
T P Dryja, T L McGee, L B Hahn, et al.
Page
of 94