RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family.

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A differential diagnosis of inherited endocrine tumors and their tumor counterparts The association between Hirschsprung's disease and multiple endocrine neoplasia type 2a: a systematic review.

P2860

Q37023603-DFF99417-002E-42DB-B00F-282AC116BB7B Q38223912-13F86E39-BD3B-48CC-B1B1-E9371B041788

P2860

RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family.

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http://www.wikidata.org/entity/Q38010028

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article scientifique

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articolo scientifico

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artigo científico

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RET haplotype, not linked to t ...... isease in a novel MEN2 family.

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type

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RET haplotype, not linked to t ...... isease in a novel MEN2 family.

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RET haplotype, not linked to t ...... isease in a novel MEN2 family.

@en

P1476

RET haplotype, not linked to t ...... isease in a novel MEN2 family.

@en

P2093

Elisangela P S Quedas

http://www.w3.org/2001/XMLSchema#string

Flavia L Coutinho

http://www.w3.org/2001/XMLSchema#string

Rodrigo A Toledo

http://www.w3.org/2001/XMLSchema#string

Sergio P A Toledo

http://www.w3.org/2001/XMLSchema#string

Tomoko Sekiya

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Uenis Tannuri

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Viviane C Longuini

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P275

Creative Commons Attribution-NonCommercial 3.0 Unported

P2860

The RET proto-oncogene induces apoptosis: a novel mechanism for Hirschsprung disease

Multiple endocrine neoplasia type 2: achievements and current challenges

Novel mutations at RET ligand genes preventing receptor activation are associated to Hirschsprung's disease

Constitutive RET tyrosine kinase activation in hereditary medullary thyroid cancer: clinical opportunities.

Gastrointestinal manifestations of multiple endocrine neoplasia type 2.

Sporadic medullary thyroid carcinoma: clinical data from a university hospital

A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.

Hirschsprung disease, associated syndromes, and genetics: a review.

Hirschsprung disease, associated syndromes and genetics: a review.

Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.

P304

57-61

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scholarly article

review article

P356

10.6061/CLINICS/2012(SUP01)11

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P478

67 Suppl 1

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P5008

ScienceSource

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2012-01-01T00:00:00Z

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P698

22584707

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P921

Hirschsprung's disease

cell surface receptor

genetic variation

membrane proteins

multiple endocrine neoplasia type 2A

proto-oncogene proteins

P932

3328835

http://www.w3.org/2001/XMLSchema#string

RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family.

about

P2860

P2860

RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family.

description

name

type

label

prefLabel

P1433

P1476

P2093

P275

P2860

P304

P31

P356

P478

P5008

P577

P698

P921

P932

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P1433

P1476

P2093

P275

P2860

P304

P31

P356

P478

P5008

P577

P698

P921

P932