(Q30848681)

27 June 2017

1 reference

title

Combined pituitary hormone deficiency: current and future status (English)

1 reference

27 June 2017

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

M-H Quentien

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Alexandru Saveanu

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Anne Barlier

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Thierry Brue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

author name string

R Reynaud

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

N Jullien

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

E Marquant

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

C Rochette

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

J-P Herman

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

A Enjalbert

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

publication date

9 September 2014

1 reference

Journal of Endocrinological Investigation

27 June 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

volume

38

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25200994%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

page(s)

1-12

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https://scigraph.springernature.com/pub.10.1007/s40618-014-0141-2

1 June 2020

exact match

0 references

cites work

Genetic regulation of pituitary gland development in human and mouse

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Induction and specification of cranial placodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Early development of the pituitary gland: induction and shaping of Rathke's pouch.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

SOX2-expressing progenitor cells generate all of the major cell types in the adult mouse pituitary gland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Genetic approaches identify adult pituitary stem cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

A GRFa2/Prop1/stem (GPS) cell niche in the pituitary

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Tissue interactions in the induction of anterior pituitary: role of the ventral diencephalon, mesenchyme, and notochord

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

In situ hybridization analysis of anterior pituitary hormone gene expression during fetal mouse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The use of neuroimaging for assessing disorders of pituitary development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Genetics of septo-optic dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

PROKR2 variants in multiple hypopituitarism with pituitary stalk interruption.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The homeobox gene Hesx1 is required in the anterior neural ectoderm for normal forebrain formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Sequence, genomic organization, and expression of the novel homeobox gene Hesx1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Hesx1, a homeobox gene expressed by murine embryonic stem cells, maps to mouse chromosome 14, bands A3-B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Alu-element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Septo-optic dysplasia - novel insights into the aetiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

21 January 2018

Septo-optic dysplasia

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Multistep signaling requirements for pituitary organogenesis in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Otx2 induction of the gonadotropin-releasing hormone promoter is modulated by direct interactions with Grg co-repressors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

OTX2 mutation in a patient with anophthalmia, short stature, and partial growth hormone deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

PITX genes are required for cell survival and Lhx3 activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

A familial syndrome of isolated "aplasia" of the anterior pituitary. Diagnostic studies and treatment in the neonatal period

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Multistep control of pituitary organogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Molecular and Clinical Findings in Patients with LHX4 and OTX2 Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

LIM homeodomain factors Lhx3 and Lhx4 assign subtype identities for motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Diverse expression patterns of LIM-homeodomain transcription factors (LIM-HDs) in mammalian inner ear development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Expression of LHX3 and SOX2 during mouse inner ear development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Conserved regulatory elements establish the dynamic expression of Rpx/HesxI in early vertebrate development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Mouse GnRH receptor gene expression is mediated by the LHX3 homeodomain protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The LIM-homeodomain proteins Isl-1 and Lhx3 act with steroidogenic factor 1 to enhance gonadotrope-specific activity of the gonadotropin-releasing hormone receptor gene promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Regulation of the follicle-stimulating hormone beta gene by the LHX3 LIM-homeodomain transcription factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The LIM homeobox protein mLIM3/Lhx3 induces expression of the prolactin gene by a Pit-1/GHF-1-independent pathway in corticotroph AtT20 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Mutations in the LHX3 gene cause dysregulation of pituitary and neural target genes that reflect patient phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

LHX3 transcription factor mutations associated with combined pituitary hormone deficiency impair the activation of pituitary target genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

A point mutation in the LIM domain of Lhx3 reduces activation of the glycoprotein hormone alpha-subunit promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

A novel mutation in the LIM homeobox 3 gene is responsible for combined pituitary hormone deficiency, hearing impairment, and vertebral malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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/10.1007%2FS40618-014-0141-2

PROP1 coexists with SOX2 and induces PIT1-commitment cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Identification and analysis of prophet of Pit-1-binding sites in human Pit-1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Long bone fracture healing: IGF-I concentrations and specific binding to erythrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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/10.1007%2FS40618-014-0141-2

A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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%2FS40618-014-0141-2

Case seminar: a young female with acute hyponatremia and a sellar mass.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

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/10.1007%2FS40618-014-0141-2

Premature differentiation and aberrant movement of pituitary cells lacking both Hes1 and Prop1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Dissection of functional domains of the pituitary-specific transcription factor GHF-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

The POU-specific domain of Pit-1 is essential for sequence-specific, high affinity DNA binding and DNA-dependent Pit-1-Pit-1 interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Pit-1 binding to specific DNA sites as a monomer or dimer determines gene-specific use of a tyrosine-dependent synergy domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

Functions of PIT1 in GATA2-dependent transactivation of the thyrotropin beta promoter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40618-014-0141-2

LIM factor Lhx3 contributes to the specification of motor neuron and interneuron identity through cell-type-specific protein-protein interactions

21 January 2018

1 reference

12 December 2020

Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency

1 reference

12 December 2020

Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia

1 reference

12 December 2020

Pit-1 and pituitary function

1 reference

12 December 2020

Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiency

1 reference

12 December 2020

A Familial Form of Congenital Hypopituitarism Due to aPROP1Mutation in a Large Kindred: Phenotypic andin VitroFunctional Studies

1 reference

12 December 2020

MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations

1 reference

12 December 2020

Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism?

1 reference

12 December 2020

Cardiovascular anomaly in Rieger Syndrome: heterogeneity or contiguity?

1 reference

12 December 2020

An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain

1 reference

12 December 2020

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

1 reference

12 December 2020

A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction

1 reference

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

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency

1 reference

12 December 2020

Domains of Pit-1 required for transcriptional synergy with GATA-2 on the TSH beta gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders

1 reference

12 December 2020

A Novel Dysfunctional LHX4 Mutation with High Phenotypical Variability in Patients with Hypopituitarism

1 reference

12 December 2020

High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency

1 reference

12 December 2020

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

1 reference

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

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

1 reference

12 December 2020

The Pitx2 protein in mouse development

1 reference

12 December 2020

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

12 December 2020

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

12 December 2020

Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype

1 reference

12 December 2020

Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT)

1 reference

12 December 2020

Differential splicing of the GHF1 primary transcript gives rise to two functionally distinct homeodomain proteins

1 reference

12 December 2020

Déficit hypophysaire combiné multiple : aspects cliniques et génétiques

1 reference

12 December 2020

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

1 reference

12 December 2020