About: Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases

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description	artículu científicu espublizáu en 1996 (ast) vědecký článek publikovaný v roce 1996 (cs) مقالة علمية (نشرت عام 1996) (ar) 1996 թվականի հունվարին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в січні 1996 (uk) 1996 թուականի Յունուարին հրատարակուած գիտական յօդուած (hyw) vedecký článok (publikovaný 1996/01/01) (sk) wetenschappelijk artikel (gepubliceerd op 1996/01/01) (nl) scientific journal article (en) im Januar 1996 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28506454-57EC306E-8B24-4F29-97E7-573318590BA8
publication date	1996-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q28506454-0967F809-D1D2-4A65-8014-10517DA3F50D wds:Q28506454-295FF3C3-DECF-4252-A5F2-8D6DF8E13CAA wds:Q28506454-2FC089AA-78D0-49C3-90B6-FD09AB796C77 wds:Q28506454-301070FD-F1B8-4C89-9B10-9D3F3FB30BCA wds:Q28506454-38BB5587-04F0-4D3B-8355-4AF070C614CD wds:Q28506454-3D337242-C950-46F3-ABE9-41874DC5043F wds:Q28506454-451022CF-80BD-46F3-A63D-CEDFB928ABAC wds:Q28506454-4739EC91-2715-4578-A01C-0333BFD1A984 wds:Q28506454-63C6A186-E020-4BBE-8048-2D2F569E6DDD wds:Q28506454-6D4E14EF-96ED-4360-9313-85098E684E19 wds:Q28506454-70957E79-8860-4A75-8614-9C74AE2FBA91 wds:Q28506454-78AE0FA8-316A-4BA7-A156-9FBDCD19146C wds:Q28506454-810BCEFA-5E73-47DE-A653-AF148B7020CD wds:Q28506454-8272F70D-BA46-4223-A8A0-ACC7890F5159 wds:Q28506454-974B5164-913D-4D94-8E88-F9EF9D6524E8 wds:Q28506454-A720AA08-F8C8-4883-9B54-55E97484F107 wds:Q28506454-A76DD4D5-4141-41BD-86CE-F8C9BFF60FE3 wds:Q28506454-AF4E9371-87E7-4609-90CA-9A9AF87BBB4A wds:Q28506454-C3B5A923-3EE4-42FA-9EDD-681E43C4847B wds:Q28506454-EB4AB8B7-D29E-4FB2-84BB-3505BED565BC wds:Q28506454-F0AD8B30-67D9-4948-905B-A008A6A2E08C wds:Q28506454-F10264DA-3B66-4EC0-81EF-5E7E7953689A wds:Q28506454-F3E64083-6E46-4CF8-93B0-980308702879
cites work	Derivation of completely cell culture-derived mice from early-passage embryonic stem cells Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat cats GM 2 Ganglioside Lysosomal Storage Disease in Cats with α-Hexosaminidase Deficiency GM2 gangliosidosis in a Japanese spaniel Purification and characterization of beta-N-acetylhexosaminidase I2 from human liver AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2 Enzyme alterations and lipid storage in three variants of Tay-Sachs disease The modular cerebellum Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice Neural progenitor cell engraftment corrects lysosomal storage throughout the MPS VII mouse brain Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism Biochemical and immunological studies on two distinct ganglioside-hydrolyzing sialidases from the particulate fraction of rat brain. Neuroaxonal dystrophy in neuronal storage disorders: evidence for major GABAergic neuron involvement. The role(s) of gangliosides in neural differentiation and repair: a perspective Clinical and Biochemical Abnormalities in Porcine GM2-Gangliosidosis Initiation and growth of ectopic neurites and meganeurites during postnatal cortical development in ganglioside storage disease Topographical atlas of the gangliosides of the adult human brain. Cloning and sequence analysis of a cDNA encoding the alpha-subunit of mouse beta-N-acetylhexosaminidase and comparison with the human enzyme Cloning and sequence analysis of a cDNA encoding the beta-subunit of mouse beta-hexosaminidase Identification of beta-N-acetylhexosaminidase A in mouse tissues with the fluorigenic substrate 4-methylumbelliferyl-beta-N-acetylglucosamine 6-sulphate Structural organization, sequence, and expression of the mouse HEXA gene encoding the alpha subunit of hexosaminidase A.
author name string	wds:Q28506454-1C29F0DF-B4E5-4E1D-A31C-E322C995D201 wds:Q28506454-3495ED5D-8135-480E-AF6F-028CED7D03C4 wds:Q28506454-3DE7169F-5990-4468-9506-16574D7587D1 wds:Q28506454-5172C6F6-A2AC-4658-AB4B-B1E2B9B4B20E wds:Q28506454-8AE48D74-E09A-4F90-B8B6-3E66BA616C58 wds:Q28506454-8B69B1FD-B065-4647-8BD0-E2FE49204FE6 wds:Q28506454-8D7A5000-EF75-484C-A3C7-1EC60E2D29D4 wds:Q28506454-9594D7DF-C3FB-4CC6-9F91-3ED7BAD57941 wds:Q28506454-9B6A0270-E4C9-4DF5-B053-11F427BA4384 wds:Q28506454-AAF1BF72-EBDA-46B6-B099-BA3C89AC507C wds:Q28506454-C77872B4-A7F7-4160-8715-C4D996F27933 wds:Q28506454-CD02FBA4-EF67-4689-B7B2-40CC3652BA9A wds:Q28506454-D3DD48E3-6799-4767-905F-B582841EFD48 wds:Q28506454-E0C3424E-0124-4CFB-A21A-930EE6BD633E wds:Q28506454-F6165449-5100-4D84-BF35-BE867E97188E wds:Q28506454-FE63080B-60A2-4493-A821-CCE11629BC69
OpenCitations bibliographic resource ID	wds:Q28506454-30FCC169-3B06-4ED4-8F83-9A865E3948E2
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/4472560
author name string	A. Borowski G. Benoit R. A. Gravel N. Hanai D. Leclerc G. Ritter J. M. Trasler N. Wakamatsu D. Phaneuf A. C. Peterson J. D. Marth C. R. Morales B. R. Akerman J. Q. Huang S. R. Fortunato S. A. Igdoura
OpenCitations bibliographic resource ID	4472560
rdfs:label	Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (en) Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (nl) Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (ast)
skos:prefLabel	Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (en) Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (nl) Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (ast)

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