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A Nechiporuk

Showing results (11-20 of 24) with videos related to

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Human Molecular Genetics|December 1, 1993
CA-repeat polymorphism at the D22S430 locus adjacent to NF2J Sainz, A Nechiporuk, U J Kim, et al.
Human Molecular Genetics|July 21, 1998
The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expressionT Nechiporuk, D P Huynh, K Figueroa, et al.
Voenno-Meditsinskii Zhurnal|October 1, 1995
[The respiratory recovery therapy of respiratory failure in the sanatorium rehabilitation of pulmonary patients]Iu N Savvin, L M Kliachkin, S A Nechiporuk, et al.
Developmental Biology|June 6, 2000
Roles for Fgf signaling during zebrafish fin regenerationK D Poss, J Shen, A Nechiporuk, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D22S351 locusJ Sainz, M Rasmussen, A Nechiporuk, et al.
Nature Communications|October 1, 2024
Cryo-EM structures of the human P2X1 receptor reveal subtype-specific architecture and antagonism by supramolecular ligand-bindingAdam C Oken, Nicolas E Lisi, Ismayn A Ditter, et al.
American Journal of Ophthalmology|November 1, 1995
Ocular abnormalities in neurofibromatosis 2N K Ragge, M E Baser, J Klein, et al.
American Journal of Medical Genetics|May 1, 1993
Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scoresA Nechiporuk, P Fain, E Kort, et al.
Neurology|November 1, 1996
Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinationsM E Baser, V F Mautner, N K Ragge, et al.
Human Genetics|April 1, 1996
Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical mapT Nechiporuk, A Nechiporuk, X Guan, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|December 1, 1993
CA-repeat polymorphism at the D22S430 locus adjacent to NF2J Sainz, A Nechiporuk, U J Kim, et al.
Human Molecular Genetics|July 21, 1998
The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expressionT Nechiporuk, D P Huynh, K Figueroa, et al.
Voenno-Meditsinskii Zhurnal|October 1, 1995
[The respiratory recovery therapy of respiratory failure in the sanatorium rehabilitation of pulmonary patients]Iu N Savvin, L M Kliachkin, S A Nechiporuk, et al.
Developmental Biology|June 6, 2000
Roles for Fgf signaling during zebrafish fin regenerationK D Poss, J Shen, A Nechiporuk, et al.
Human Molecular Genetics|October 1, 1993
Dinucleotide repeat polymorphism at the D22S351 locusJ Sainz, M Rasmussen, A Nechiporuk, et al.
Nature Communications|October 1, 2024
Cryo-EM structures of the human P2X1 receptor reveal subtype-specific architecture and antagonism by supramolecular ligand-bindingAdam C Oken, Nicolas E Lisi, Ismayn A Ditter, et al.
American Journal of Ophthalmology|November 1, 1995
Ocular abnormalities in neurofibromatosis 2N K Ragge, M E Baser, J Klein, et al.
American Journal of Medical Genetics|May 1, 1993
Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scoresA Nechiporuk, P Fain, E Kort, et al.
Neurology|November 1, 1996
Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinationsM E Baser, V F Mautner, N K Ragge, et al.
Human Genetics|April 1, 1996
Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical mapT Nechiporuk, A Nechiporuk, X Guan, et al.
Pageof 3