Hepatocyte Nuclear Factor 1β-Associated Kidney Disease: More than Renal Cysts and Diabetes. (Q36514988)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26319241%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

title

Hepatocyte Nuclear Factor 1β-Associated Kidney Disease: More than Renal Cysts and Diabetes (English)

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23 February 2020

1 reference

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4

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23 February 2020

1

Jacobien C Verhave

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23 February 2020

author name string

Anneke P Bech

series ordinal

2

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23 February 2020

Jack F M Wetzels

series ordinal

3

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23 February 2020

publication date

28 August 2015

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26319241%20AND%20SRC:MED&resulttype=core&format=json

Journal of the American Society of Nephrology

23 February 2020

language of work or name

English

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published in

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23 February 2020

volume

27

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23 February 2020

issue

2

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23 February 2020

page(s)

345-353

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Genomic imbalances in pediatric patients with chronic kidney disease

23 February 2020

cites work

1 reference

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30 September 2017

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30 September 2017

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30 September 2017

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HNF-1B specifically regulates the transcription of the γa-subunit of the Na+/K+-ATPase

30 September 2017

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

30 September 2017

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

30 September 2017

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Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.

30 September 2017

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HNF1B mutations associate with hypomagnesemia and renal magnesium wasting

30 September 2017

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Roles of HNF-1beta in kidney development and congenital cystic diseases

30 September 2017

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Lack of TCF2/vHNF1 in mice leads to pancreas agenesis

30 September 2017

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Role of the hepatocyte nuclear factor-1beta (HNF-1beta) C-terminal domain in Pkhd1 (ARPKD) gene transcription and renal cystogenesis

30 September 2017

1 reference

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Neonatal Diabetes Mellitus and Neonatal Polycystic, Dysplastic Kidneys: Phenotypically Discordant Recurrence of a Mutation in the Hepatocyte Nuclear Factor-1β Gene Due to Germline Mosaicism

30 September 2017

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Expression profiling in ovarian clear cell carcinoma: identification of hepatocyte nuclear factor-1 beta as a molecular marker and a possible molecular target for therapy of ovarian clear cell carcinoma

30 September 2017

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

30 September 2017

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Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations

30 September 2017

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Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease

30 September 2017

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Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit

30 September 2017

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

30 September 2017

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

30 September 2017

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Identification of transacting factors responsible for the tissue-specific expression of human glucose transporter type 2 isoform gene. Cooperative role of hepatocyte nuclear factors 1alpha and 3beta

28 June 2018

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Frameshift Mutation, A263fsinsGG, in the Hepatocyte Nuclear Factor-1β Gene Associated With Diabetes and Renal Dysfunction

28 June 2018

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Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.

28 June 2018

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28 June 2018

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Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tract

28 June 2018

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Early development of hyperparathyroidism due to loss of PTH transcriptional repression in patients with HNF1β mutations?

21 September 2018

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Hepatocyte nuclear factor 1β controls nephron tubular development

21 September 2018

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Hepatocyte nuclear factor 1β is a novel prognostic marker independent of the milan criteria in transplantable hepatocellular carcinoma: A retrospective analysis based on tissue microarrays

21 September 2018

1 reference

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

21 September 2018

1 reference

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HNF1B alterations associated with congenital anomalies of the kidney and urinary tract

21 September 2018

1 reference

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HNF1beta and defective nephrogenesis: a role for interacting partners?

21 September 2018

1 reference

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

21 September 2018

1 reference

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

21 September 2018

1 reference

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Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations

21 September 2018

1 reference

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Expression of bile duct transcription factor HNF1β predicts early tumor recurrence and is a stage-independent prognostic factor in hepatocellular carcinoma

21 September 2018

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Underexpression of hepatocyte nuclear factor-1β in chromophobe renal cell carcinoma

21 October 2018

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

A genetic syndrome of chronic renal failure with multiple renal cysts and early onset diabetes

1 reference

12 December 2020

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood

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12 December 2020

Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)

1 reference

12 December 2020

Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: a single centre cohort analysis

1 reference

12 December 2020

Diabetes-Induced Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): Nurture and Nature at Work?

1 reference

12 December 2020

Identifiers

DOI

10.1681/ASN.2015050544

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26319241%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26319241%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

PubMed publication ID

26319241

1 reference