(Q48418100)

11 February 2018

title

PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency. (English)

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11 February 2018

author

Manuel C. Lemos

1

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11 February 2018

Leonor Gomes

2

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11 February 2018

Valeriano Leite

4

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11 February 2018

Davide Carvalho

6

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11 February 2018

Mariana P. Monteiro

8

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11 February 2018

Fernando Regateiro

12

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11 February 2018

author name string

Margarida Bastos

3

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11 February 2018

Edward Limbert

5

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11 February 2018

Conceição Bacelar

7

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11 February 2018

Fernando Fonseca

9

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11 February 2018

Ana Agapito

10

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11 February 2018

João J Castro

11

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11 February 2018

Manuela Carvalheiro

13

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11 February 2018

publication date

1 October 2006

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11 February 2018

published in

Clinical Endocrinology

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11 February 2018

volume

65

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11 February 2018

issue

4

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11 February 2018

page(s)

479-485

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11 February 2018

Human Prop-1: cloning, mapping, genomic structure

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Transcriptional control during mammalian anterior pituitary development

21 January 2018

1 reference

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Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

The spectrum of hypopituitarism caused by PROP1 mutations

21 January 2018

1 reference

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Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Pseudotumor of the pituitary due to PROP-1 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Emerging links between initiation of translation and human diseases

21 January 2018

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Interpreting cDNA sequences: some insights from studies on translation

21 January 2018

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Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Phenotypic Variability in Familial Combined Pituitary Hormone Deficiency Caused by a PROP1 Gene Mutation Resulting in the Substitution of Arg->Cys at Codon 120 (R120C)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

A novel PROP1 gene mutation (157delA) in Japanese siblings with combined anterior pituitary hormone deficiency.

21 January 2018

1 reference

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PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02617.X

10.1111/J.1365-2265.2006.02617.X

21 January 2018

Identifiers

DOI

1 reference

11 February 2018

PubMed ID

16984240

1 reference

11 February 2018