(Q28275998)

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Identification of a structural requirement for thyroid Na+/I- symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9657379%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Identification of a structural requirement for thyroid Na+/I- symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9657379%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

congenital disorder

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congenital hypothyroidism

1 reference

based on heuristic

inferred from title

Antonio De la Vieja

3

1 reference

Europe PubMed Central

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12 November 2019

author name string

O Levy

1

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12 November 2019

C S Ginter

2

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12 November 2019

D Levy

4

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12 November 2019

N Carrasco

5

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12 November 2019

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publication date

1 June 1998

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12 November 2019

1 reference

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12 November 2019

429

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12 November 2019

1

1 reference

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12 November 2019

36-40

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12 November 2019

Congenital hypothyroidism caused by a mutation in the Na+/I- symporter

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Cloning and characterization of the thyroid iodide transporter

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Congenital Goiter with Defective Iodide Transport

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Complete iodide trapping defect in two cases with congenital hypothyroidism: adaptation of thyroid to huge iodide supplementation

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Cloning of the human sodium lodide symporter

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Characterization of the thyroid Na+/I- symporter with an anti-COOH terminus antibody

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900522-5

7 January 2021

Identifiers

10.1016/S0014-5793(98)00522-5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9657379%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9657379%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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