(Q34180055)

31 July 2017

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse (English)

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31 July 2017

3

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31 July 2017

Peeters H

1

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31 July 2017

Debeer P

2

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31 July 2017

Wilquet V

4

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31 July 2017

Huysmans C

5

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31 July 2017

Parthoens E

6

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31 July 2017

Fryns JP

7

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31 July 2017

Gewillig M

8

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31 July 2017

Nakamura Y

9

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31 July 2017

Niikawa N

10

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31 July 2017

Van de Ven W

11

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31 July 2017

Devriendt K

12

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31 July 2017

27 February 2003

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31 July 2017

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31 July 2017

112

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31 July 2017

573-580

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31 July 2017

5-6

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https://scigraph.springernature.com/pub.10.1007/s00439-003-0917-5

31 July 2017

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cites work

Analysis of clinical variation seen in patients with 18q terminal deletions

1 reference

12 December 2020

A molecular pathway determining left-right asymmetry in chick embryogenesis

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12 December 2020

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region

1 reference

12 December 2020

Identification of a novel stress-responsive gene Hi95 involved in regulation of cell viability.

1 reference

12 December 2020

Mechanisms of left-right asymmetry: what's right and what's left?

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12 December 2020

The human genome browser at UCSC

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12 December 2020

Role of notochord in specification of cardiac left-right orientation in zebrafish and Xenopus.

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12 December 2020

Recurrent involvement of chromosomal region 6q21 in heterotaxy.

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12 December 2020

A Xenopus homolog of a human p53-activated gene, PA26, is specifically expressed in the notochord

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12 December 2020

Positional cloning moves from perditional to traditional

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12 December 2020

Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB

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12 December 2020

Axis development and early asymmetry in mammals

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12 December 2020

De novo balanced translocation (6;18)(q21;q21.3 or q22) [corrected] in a patient with heterotaxia.

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12 December 2020

Floor plate and motor neuron induction by vhh-1, a vertebrate homolog of hedgehog expressed by the notochord

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12 December 2020

Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development.

1 reference

12 December 2020

Experimental analysis of the emergence of left-right asymmetry of the body axis in early postimplantation mouse embryos.

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12 December 2020

Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21

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12 December 2020

The HUGO Gene Nomenclature Committee (HGNC).

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12 December 2020

PA26, a novel target of the p53 tumor suppressor and member of the GADD family of DNA damage and growth arrest inducible genes

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12 December 2020

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

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12 December 2020

Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.

1 reference

12 December 2020

Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).

1 reference

12 December 2020

Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1

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12 December 2020

X-linked situs abnormalities result from mutations in ZIC3

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12 December 2020

The transfer of left-right positional information during chick embryogenesis

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12 December 2020

The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

1 reference

12 December 2020

A study of Xlim1 function in the Spemann-Mangold organizer

1 reference

12 December 2020

10.1007/S00439-003-0917-5

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