(Q54129199)

English

Genetic complementation after fusion of Tay-Sachs and Sandhoff cells.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

Genetic complementation after fusion of Tay-Sachs and Sandhoff cells. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

author name string

Thomas GH

1

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

Taylor HA

2

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

Miller CS

3

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

Axelman J

4

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

Migeon BR

5

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

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publication date

1 August 1974

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

250

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

467

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

580-582

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

https://scigraph.springernature.com/pub.10.1038/250580a0

0 references

Electrophoretic study of hexosaminidases. Hexosaminidase C.

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Antibody against purified human hexosaminidase B cross-reacting with human hexosaminidase A

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Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

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7 January 2021

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Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs

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Lysosomal hydrolases: Conversion of acidic to basic forms by neuraminidase

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Tay-Sachs disease: interrelation of hexosaminidases A and B

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On the molecular basis of Sandhoff's disease

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Poliovirus replication and cytopathogenicity in monolayer hamster cell cultures fused with beta propiolactone-inactivated Sendai virus.

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Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.

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Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase Activity

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Genetic Heterogeneity of Xeroderma Pigmentosum demonstrated by Somatic Cell Hybridization

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Complementation Analysis of Maple Syrup Urine Disease in Heterokaryons derived from Cultured Human Fibroblasts

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Identifiers

10.1038/250580A0

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4367631

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