(Q54441396)

29 May 2018

title

HNF1B alterations associated with congenital anomalies of the kidney and urinary tract. (English)

1 reference

29 May 2018

author name string

Makiko Nakayama

1

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29 May 2018

Kandai Nozu

2

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29 May 2018

Yuki Goto

3

1 reference

29 May 2018

Koichi Kamei

4

1 reference

29 May 2018

Shuichi Ito

5

1 reference

29 May 2018

Hidenori Sato

6

1 reference

29 May 2018

Mitsuru Emi

7

1 reference

29 May 2018

Koichi Nakanishi

8

1 reference

29 May 2018

Shigeru Tsuchiya

9

1 reference

29 May 2018

Kazumoto Iijima

10

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29 May 2018

publication date

13 February 2010

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29 May 2018

published in

Pediatric Nephrology

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29 May 2018

volume

25

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29 May 2018

issue

6

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29 May 2018

page(s)

1073-1079

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29 May 2018

https://scigraph.springernature.com/pub.10.1007/s00467-010-1454-9

exact match

0 references

cites work

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Distinct and sequential tissue-specific activities of the LIM-class homeobox gene Lim1 for tubular morphogenesis during kidney development

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Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT)

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HNF1B mutations associate with hypomagnesemia and renal magnesium wasting

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

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

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Studies of the variability of the hepatocyte nuclear factor-1beta (HNF-1beta / TCF2) and the dimerization cofactor of HNF-1 (DcoH / PCBD) genes in relation to type 2 diabetes mellitus and beta-cell function

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

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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.

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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

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Lim 1 is required for nephric duct extension and ureteric bud morphogenesis

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Essential role for the homeoprotein vHNF1/HNF1beta in visceral endoderm differentiation

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12 December 2020

10.1007/S00467-010-1454-9

Identifiers

DOI

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29 May 2018

PubMed ID

20155289

1 reference

29 May 2018