(Q84580181)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

title

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

Jean-Philippe Lengelé

8

1 reference

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8 February 2020

author name string

Stanislas Faguer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Stéphane Decramer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Nicolas Chassaing

3

1 reference

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8 February 2020

Christine Bellanné-Chantelot

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Patrick Calvas

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Sandrine Beaufils

6

1 reference

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8 February 2020

Lucie Bessenay

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Karine Dahan

9

1 reference

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8 February 2020

Pierre Ronco

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

Olivier Devuyst

11

1 reference

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8 February 2020

Dominique Chauveau

12

1 reference

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8 February 2020

language of work or name

English

0 references

publication date

20 July 2011

1 reference

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8 February 2020

1 reference

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8 February 2020

volume

80

1 reference

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8 February 2020

issue

7

1 reference

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8 February 2020

page(s)

768-776

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21775974%20AND%20SRC:MED&resulttype=core&format=json

Two members of an HNF1 homeoprotein family are expressed in human liver

8 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Expression of the vHNF1/HNF1beta homeoprotein gene during mouse organogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Distinct roles of HNF1beta, HNF1alpha, and HNF4alpha in regulating pancreas development, beta-cell function and growth.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Mutations in hepatocyte nuclear factor-1beta and their related phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Hepatocyte nuclear factor-1beta gene deletions--a common cause of renal disease.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1beta.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Anomalies of the TCF2 Gene Are the Main Cause of Fetal Bilateral Hyperechogenic Kidneys

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

HNF1B mutations associate with hypomagnesemia and renal magnesium wasting

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Neonatal cholestatic jaundice as the first symptom of a mutation in the hepatocyte nuclear factor-1beta gene (HNF-1beta)

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Exonic duplication of the hepatocyte nuclear factor-1beta gene (transcription factor 2, hepatic) as a cause of maturity onset diabetes of the young type 5

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Massively enlarged polycystic kidneys in monozygotic twins with TCF2/HNF-1beta (hepatocyte nuclear factor-1beta) heterozygous whole-gene deletion

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Severe pancreas hypoplasia and multicystic renal dysplasia in two human fetuses carrying novel HNF1beta/MODY5 mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Cystic kidney disease, chromophobe renal cell carcinoma and TCF2 (HNF1 beta) mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

New molecular players facilitating Mg(2+) reabsorption in the distal convoluted tubule

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Magnesium Modulates ROMK Channel–Mediated Potassium Secretion

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

The mouse alpha-albumin (afamin) promoter is differentially regulated by hepatocyte nuclear factor 1α and hepatocyte nuclear factor 1β

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

A mitotic transcriptional switch in polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Germline hepatocyte nuclear factor 1alpha and 1beta mutations in renal cell carcinomas.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.225

7 January 2021

A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group

1 reference

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7 January 2021