(Q42443191)

English

Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 gene

scientific article published on January 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

1 reference

based on heuristic

inferred from title

4

object named as

Kiess W

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

author name string

Lamesch C

1

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Neumann S

2

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Pfäffle R

3

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Paschke R

5

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

publication date

1 January 2002

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Europe PubMed Central

PubMed publication ID

31 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

163-168

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of combined pituitary hormone deficiencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis for developmental disorders of the pituitary gland in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prop-1 gene expression in human pituitary tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable disorders of pituitary development

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in PROP1 cause familial combined pituitary hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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)

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anterior pituitary cell population control: basal cell turnover and the effects of adrenalectomy and dexamethasone treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12812307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1023356915458

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

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