(Q35764727)

English

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats

scientific article published on 15 March 2002

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scholarly article

1 reference

Europe PubMed Central

10 August 2017

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats (English)

1 reference

Europe PubMed Central

10 August 2017

object named as

Luiz F Onuchic

1

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Gregory Germino

object named as

Gregory G Germino

18

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object named as

Jan Senderek

8

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author name string

Laszlo Furu

2

1 reference

Europe PubMed Central

10 August 2017

Yasuyuki Nagasawa

3

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Europe PubMed Central

10 August 2017

Xiaoying Hou

4

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Europe PubMed Central

10 August 2017

Thomas Eggermann

5

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Europe PubMed Central

10 August 2017

Zhiyong Ren

6

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Europe PubMed Central

10 August 2017

Carsten Bergmann

7

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Europe PubMed Central

10 August 2017

Ernie Esquivel

9

1 reference

Europe PubMed Central

10 August 2017

Raoul Zeltner

10

1 reference

Europe PubMed Central

10 August 2017

Sabine Rudnik-Schöneborn

11

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Europe PubMed Central

10 August 2017

Michael Mrug

12

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Europe PubMed Central

10 August 2017

William Sweeney

13

1 reference

Europe PubMed Central

10 August 2017

Ellis D Avner

14

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10 August 2017

Klaus Zerres

15

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10 August 2017

Lisa M Guay-Woodford

16

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10 August 2017

Stefan Somlo

17

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Europe PubMed Central

10 August 2017

language of work or name

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publication date

15 March 2002

1 reference

Europe PubMed Central

10 August 2017

American Journal of Human Genetics

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Europe PubMed Central

10 August 2017

70

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10 August 2017

1305-1317

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10 August 2017

5

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Europe PubMed Central

10 August 2017

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Recent improvements to the SMART domain-based sequence annotation resource

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

The Sequence of the Human Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Ab initio gene finding in Drosophila genomic DNA

1 reference

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2 October 2017

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Genomic organization of the KIAA0057 gene that encodes a TRAM-like protein and its exclusion as a polycystic kidney and hepatic disease 1 (PKHD1) candidate gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

SMART, a simple modular architecture research tool: identification of signaling domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2 beta, and GSTA1 at 6p21.1-p12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Neurexins: three genes and 1001 products

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Prediction of complete gene structures in human genomic DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft für Pädiatrische, Nephrologie

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Polycystic kidney disease: primary extracellular matrix abnormality or defective cellular differentiation?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12: implications for genetic counseling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

2 October 2017

Structure of the human NF-kappaB p52 homodimer-DNA complex at 2.1 A resolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

27 July 2018

Identification of a novel cytokine, ML-1, and its expression in subjects with asthma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

25 September 2018

Evaluation of gene structure prediction programs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

25 September 2018

Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447605

23 October 2018

Somatic inactivation of Pkd2 results in polycystic kidney disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 1-Mb BAC/PAC-based physical map of the autosomal recessive polycystic kidney disease gene (PKHD1) region on chromosome 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abdominal sonographic study of autosomal dominant polycystic kidney disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand-containing gene as a PKHD1 candidate gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis by ultrasound in pregnancies at risk for autosomal recessive polycystic kidney disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An integrated genetic and physical map of the autosomal recessive polycystic kidney disease region

1 reference

https://pubmed.ncbi.nlm.nih.gov/11898128

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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