[Hox genes and genetic control of limb development]

Heterogeneous combinatorial expression of Hoxd genes in single cells during limb development.

BMC biology·2018

A molecular approach to the evolution of vertebrate paired appendages.

Trends in ecology & evolution·2011

Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations.

Genes & development·2001

The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes.

Developmental biology·2001

Impaired skin wound healing in peroxisome proliferator-activated receptor (PPAR)alpha and PPARbeta mutant mice.

The Journal of cell biology·2001

Localized and transient transcription of Hox genes suggests a link between patterning and the segmentation clock.

Cell·2001

Risk factors for pediatric community-acquired febrile urinary tract infections due to resistant bacteria and treatment options: a French retrospective case-control study (FRIUPed).

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Characterization of language profile in children with critical congenital heart disease.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Assessing the psychosocial health of adolescents with chronic diseases.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Clinical characteristics and co-infection patterns of human metapneumovirus infection in children under 5 years of age.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Pulmonary involvement in inflammatory bowel diseases: report of a national cohort over the past 5 years.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Bronchodilator reversibility in children with cystic fibrosis: prevalence and associated factors.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2026

Father-Son Comparison of Reproductive Traits.

Andrology·2026

Pediatric Gastric GIST With SDHA Truncation Despite Retained SDHB Staining: A Case Report.

Journal of pediatric hematology/oncology·2026

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Frontiers in genetics·2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Frontiers in genetics·2026

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Developmental biology·2026

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Journal of neural transmission (Vienna, Austria : 1996)·2026

Related Experiment Videos

[Hox genes and genetic control of limb development]

Related Concept Videos

Heterogeneous combinatorial expression of Hoxd genes in single cells during limb development.

A molecular approach to the evolution of vertebrate paired appendages.

Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations.

The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes.

Impaired skin wound healing in peroxisome proliferator-activated receptor (PPAR)alpha and PPARbeta mutant mice.

Localized and transient transcription of Hox genes suggests a link between patterning and the segmentation clock.

Risk factors for pediatric community-acquired febrile urinary tract infections due to resistant bacteria and treatment options: a French retrospective case-control study (FRIUPed).

Characterization of language profile in children with critical congenital heart disease.

Assessing the psychosocial health of adolescents with chronic diseases.

Clinical characteristics and co-infection patterns of human metapneumovirus infection in children under 5 years of age.

Pulmonary involvement in inflammatory bowel diseases: report of a national cohort over the past 5 years.

Bronchodilator reversibility in children with cystic fibrosis: prevalence and associated factors.

Father-Son Comparison of Reproductive Traits.

Pediatric Gastric GIST With SDHA Truncation Despite Retained SDHB Staining: A Case Report.

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Related Experiment Videos

[Hox genes and genetic control of limb development]

Related Concept Videos

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