(Q41698332)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

title

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

multicenter clinical trial

24 February 2020

main subject

0 references

author

Bilgin Yüksel

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

author name string

Firdevs Baş

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Z Oya Uyguner

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Feyza Darendeliler

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Zehra Aycan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Ergun Çetinkaya

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Merih Berberoğlu

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Zeynep Şiklar

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Gönül Öcal

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Şükran Darcan

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Damla Gökşen

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Ali Kemal Topaloğlu

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Mehmet Nuri Özbek

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Oya Ercan

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Olcay Evliyaoğlu

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Semra Çetinkaya

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Yaşar Şen

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Emre Atabek

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Güven Toksoy

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Banu Küçükemre Aydin

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Rüveyde Bundak

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

publication date

11 December 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

volume

49

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

page(s)

479-491

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25500790%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s12020-014-0498-1

24 February 2020

exact match

0 references

cites work

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21 January 2018

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21 January 2018

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Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency

21 January 2018

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Genetic regulation of pituitary gland development in human and mouse

21 January 2018

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Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms.

21 January 2018

1 reference

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A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literature

21 January 2018

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Body weight, length and head circumference at birth in a cohort of Turkish newborns

21 January 2018

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Updated growth curves for Turkish children aged 15 days to 60 months.

21 January 2018

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Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.

21 January 2018

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21 January 2018

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21 January 2018

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Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-014-0498-1

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-014-0498-1

PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency

21 January 2018

1 reference

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High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.

21 January 2018

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Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.

21 January 2018

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Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.

21 January 2018

1 reference

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Suprasellar mass mimicking a hypothalamic glioma in a patient with a complete PROP1 deletion

21 January 2018

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Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.

21 January 2018

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Congenital hypopituitarism: clinical, molecular and neuroradiological correlates

21 January 2018

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21 January 2018

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Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.

21 January 2018

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Idiopathic sexual precocity in a boy with growth hormone, prolactin and thyrotropin deficiencies.

21 January 2018

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GH deficiency with central precocious puberty: a new rare disorder associated with a developmental defect of the hypothalamic-pituitary area.

21 January 2018

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Reciprocal interactions of Pit1 and GATA2 mediate signaling gradient-induced determination of pituitary cell types

21 January 2018

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GATA transcription factors regulate LHβ gene expression

21 January 2018

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A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

21 January 2018

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A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies.

21 January 2018

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12 December 2020

Heritable disorders of pituitary development

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

12 December 2020

Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency

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12 December 2020

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12 December 2020

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12 December 2020