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Joining the fingers: a HOXD13 Story

author

Przemko Tylzanowski

published in: Developmental Dynamics

date of publication: 2014-01-01

language: English

Cites articles 77

Date

Title

Authors

2013-06-01

A switch between topological domains underlies HoxD genes collinearity in mouse limbs.

Daan Noordermeer, Thomas Montavon, Guillaume Andrey, Denis Duboule, François Spitz
2012-02-27

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning

Vincenzo Zappavigna, Przemko Tylzanowski
2012-01-10

Isolated brachydactyly type E caused by a HOXD13 nonsense mutation: a case report

Leszek Kaczmarek, Anna Latos-Bieleńska, Aleksander Jamsheer
2012-07-01

Homozygous nonsense mutation in HOXD13 underlies synpolydactyly with a cleft
2012-02-22

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

Xueya Zhou
2012-03-03

Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly
2011-07-02

Limb skeletal malformations - what the HOX is going on?

Przemko Tylzanowski
2011-06-08

Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus

Bernard Sablonniere, Jamal Ghoumid, Sylvie Manouvrier-Hanu, Muriel Holder-Espinasse, Joris Andrieux
2011-08-04

A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance
2011-03-17

How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
2010-11-10

2q31.1 microdeletion syndrome: redefining the associated clinical phenotype

Joris R Vermeesch, Thomy de Ravel
2010-10-23

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly
2010-05-10

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation

Denis Duboule, Stefan Mundlos
2010-05-27

The temporal dynamics of vertebrate limb development, teratogenesis and evolution

Rolf Zeller
2009-10

Vertebrate limb development: moving from classical morphogen gradients to an integrated 4-dimensional patterning system

Rolf Zeller
2009-09-02

Building limb morphology through integration of signalling modules
2009-05-07

Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery

Andrew Oliver Mungo Wilkie, Henk Giele
2009-04-01

The RCAS retroviral expression system in the study of skeletal development

Christopher T Gordon
2009-01-01

Hox specificity unique roles for cofactors and collaborators

Rohit Joshi
2009-05-01

A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactyly
2009-08-17

Polyalanine repeat expansion mutations in the HOXD13 gene in Pakistani families with synpolydactyly

Martha B Dua-Awereh
2008-01-01

Electroporation in avian embryos
2008-12-01

Identification of a HOXD13 mutation in a VACTERL patient

Vincent C.H. Lui, Patrick H Y Chung, Paul Kwong Hang Tam, Maria-Mercè Garcia-Barcelo, Xiao-Ping Miao, Kenneth Kak-Yuen Wong, Elly Sau-Wai Ngan, Pek-Lan Khong
2008-02-04

Germ cells and transgenesis in chickens
2008-01-01

Gain- and loss-of-function approaches in the chick embryo

Tatjana Sauka-Spengler
2007-12-11

Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences

Sajid Malik
2007-12-19

Synpolydactyly: clinical and molecular advances
2007-10-15

Hoxd and Gli3 interactions modulate digit number in the amniote limb
2007-03-01

A hypermorphic mouse Gli3 allele results in a polydactylous limb phenotype.
2007-07-20

The role of Hox genes during vertebrate limb development

Denis Duboule
2007-02

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome

L. Mario Amzel, Ethylin Wang Jabs, J Alfonso Leyva
2006-02-09

Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion

Yanick J. Crow

Article - wd:Q57921627

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