(Q37363610)

19 August 2017

1 reference

title

Interpreting neonatal lethal phenotypes in mouse mutants: insights into gene function and human diseases (English)

1 reference

19 August 2017

1 reference

Benjamin Turgeon

1

1 reference

PubMed ID

19126753

19 August 2017

Sylvain Meloche

series ordinal

2

1 reference

PubMed ID

19126753

19 August 2017

language of work or name

1 reference

1 January 2009

1 reference

19 August 2017

Physiological Reviews

1 reference

19 August 2017

89

1 reference

19 August 2017

1-26

1 reference

19 August 2017

1

1 reference

Targeted disruption of the homeobox transcription factor Bapx1 results in lethal skeletal dysplasia with asplenia and gastroduodenal malformation.

19 August 2017

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Extensive vasculogenesis, angiogenesis, and organogenesis precede lethality in mice lacking all alpha v integrins

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mice deficient in G(olf) are anosmic

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

MafB deficiency causes defective respiratory rhythmogenesis and fatal central apnea at birth

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted inactivation of the muscle regulatory gene Myf-5 results in abnormal rib development and perinatal death

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Finally, a sense of closure? Animal models of human ventral body wall defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Understanding mammalian genetic systems: the challenge of phenotyping in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

General anosmia caused by a targeted disruption of the mouse olfactory cyclic nucleotide-gated cation channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Building the mammalian heart from two sources of myocardial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Lung morphogenesis revisited: old facts, current ideas

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Craniofacial dysmorphogenesis including cleft palate in mice with an insertional mutation in the discs large gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of Huntingtin-associated protein-1 (Hap1) results in postnatal death due to depressed feeding behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Feedback control of mammalian Hedgehog signaling by the Hedgehog-binding protein, Hip1, modulates Fgf signaling during branching morphogenesis of the lung

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of the surfactant protein B gene disrupts surfactant homeostasis, causing respiratory failure in newborn mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The lipid phosphatase SHIP2 controls insulin sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Metabolism of PGE2 by prostaglandin dehydrogenase is essential for remodeling the ductus arteriosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Genetic disorders of neonatal respiratory function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of the glucocorticoid receptor gene blocks adrenergic chromaffin cell development and severely retards lung maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

21 January 2018

A Mouse for All Reasons

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Opposing actions of Arx and Pax4 in endocrine pancreas development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Cellular and molecular interactions regulating skeletogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Requirement for the lpA1 lysophosphatidic acid receptor gene in normal suckling behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

What cardiovascular defect does my prenatal mouse mutant have, and why?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Death before birth: clues from gene knockouts and mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor V

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Molecular mechanisms of liver development and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mice lacking the CNTF receptor, unlike mice lacking CNTF, exhibit profound motor neuron deficits at birth

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Transcriptional regulation of metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Impaired PtdIns(4,5)P2 synthesis in nerve terminals produces defects in synaptic vesicle trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Anuria, omphalocele, and perinatal lethality in mice lacking the CD34-related protein podocalyxin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Huntingtin-associated protein 1 (Hap1) mutant mice bypassing the early postnatal lethality are neuroanatomically normal and fertile but display growth retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of NDST-1 gene leads to pulmonary hypoplasia and neonatal respiratory distress in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mouse models and the urinary concentrating mechanism in the new millennium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Lethal impairment of cholinergic neurotransmission in hemicholinium-3-sensitive choline transporter knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Signalling interactions during facial development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mammalian genome targeting using site-specific recombinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Transgenic models to study disorders of respiratory control in newborn mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Defective neuromuscular synaptogenesis in agrin-deficient mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Failure of postsynaptic specialization to develop at neuromuscular junctions of rapsyn-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

PlexinD1 and semaphorin signaling are required in endothelial cells for cardiovascular development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Current issues in mouse genome engineering

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Inactivation of the glycine transporter 1 gene discloses vital role of glial glycine uptake in glycinergic inhibition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mouse models of neural tube defects: investigating preventive mechanisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Development gone awry: congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Nuclear factor I-B (Nfib) deficient mice have severe lung hypoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Defective lung vascular development and fatal respiratory distress in endothelial NO synthase-deficient mice: a model of alveolar capillary dysplasia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Lethal, neonatal ichthyosis with increased proteolytic processing of filaggrin in a mouse model of Netherton syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Regional regulation of palatal growth and patterning along the anterior-posterior axis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Embryonic renal epithelia: induction, nephrogenesis, and cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Malfunction of respiratory-related neuronal activity in Na+, K+-ATPase alpha2 subunit-deficient mice is attributable to abnormal Cl- homeostasis in brainstem neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Deficiency of triad junction and contraction in mutant skeletal muscle lacking junctophilin type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Connective tissue growth factor coordinates chondrogenesis and angiogenesis during skeletal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Reorganization of pontine rhythmogenic neuronal networks in Krox-20 knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Inactivation of the gene for anticoagulant protein C causes lethal perinatal consumptive coagulopathy in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of the BDNF gene perturbs brain and sensory neuron development but not motor neuron development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Reaching a genetic and molecular understanding of skeletal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Genome-wide array analysis of normal and malformed human hearts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Loss of myogenin in postnatal life leads to normal skeletal muscle but reduced body size.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Impairment of starvation-induced and constitutive autophagy in Atg7-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Glycogen autophagy in glucose homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Embryonic and neonatal phenotyping of genetically engineered mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The role of autophagy during the early neonatal starvation period

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Assembly of the postsynaptic membrane at the neuromuscular junction: paradigm lost

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Impairment of suckling response, trigeminal neuronal pattern formation, and hippocampal LTD in NMDA receptor epsilon 2 subunit mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The mouse bagpipe gene controls development of axial skeleton, skull, and spleen

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Murine models of human genetic skeletal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Tissue-specific hemostasis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Defective stratum corneum and early neonatal death in mice lacking the gene for transglutaminase 1 (keratinocyte transglutaminase)

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Disruption of the beta subunit of the epithelial Na+ channel in mice: hyperkalemia and neonatal death associated with a pseudohypoaldosteronism phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Requirement for Brn-3.0 in differentiation and survival of sensory and motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Caring for the newborn with an omphalocele

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Aberrant quality control in the endoplasmic reticulum impairs the biosynthesis of pulmonary surfactant in mice expressing mutant BiP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Roles of neurotransmitter in synapse formation: development of neuromuscular junctions lacking choline acetyltransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Stearoyl-CoA desaturase-2 gene expression is required for lipid synthesis during early skin and liver development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Dissection of autophagosome formation using Apg5-deficient mouse embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Sclerotome development and morphogenesis: when experimental embryology meets genetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Integrin alpha8beta1 is critically important for epithelial-mesenchymal interactions during kidney morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Myogenin gene disruption results in perinatal lethality because of severe muscle defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Cre recombinase: The universal reagent for genome tailoring

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Crucial roles of Brn1 in distal tubule formation and function in mouse kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Bricks and mortar of the epidermal barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The prostaglandin receptor EP4 triggers remodelling of the cardiovascular system at birth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Developmental regulation of lung liquid transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted disruption of the ATP2A1 gene encoding the sarco(endo)plasmic reticulum Ca2+ ATPase isoform 1 (SERCA1) impairs diaphragm function and is lethal in neonatal mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Null mutation of mCOUP-TFI results in defects in morphogenesis of the glossopharyngeal ganglion, axonal projection, and arborization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

T1alpha, a lung type I cell differentiation gene, is required for normal lung cell proliferation and alveolus formation at birth

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Pbx3 deficiency results in central hypoventilation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Studying rhythmogenesis of breathing: comparison of in vivo and in vitro models

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Surfactant lipid synthesis and lamellar body formation in glycogen-laden type II cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Nipple attachment and survival in neonatal olfactory bulbectomized rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Mice lacking factor VII develop normally but suffer fatal perinatal bleeding

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted gene knockout in mammalian cells by using engineered zinc-finger nucleases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Anteriorization of neural fate by inhibitor of beta-catenin and T cell factor (ICAT), a negative regulator of Wnt signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Translational control is required for the unfolded protein response and in vivo glucose homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Epidermal barrier formation and recovery in skin disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Klf4 is a transcription factor required for establishing the barrier function of the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Fgf10 is essential for limb and lung formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Hypothalamic huntingtin-associated protein 1 as a mediator of feeding behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

ROCK-I regulates closure of the eyelids and ventral body wall by inducing assembly of actomyosin bundles

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Rnx deficiency results in congenital central hypoventilation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Abnormal kidney development and hematological disorders in PDGF beta-receptor mutant mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The transcription factor gene Nfib is essential for both lung maturation and brain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

The chemokine receptor CXCR4 is essential for vascularization of the gastrointestinal tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Spontaneous muscle action potentials fail to develop without fetal-type acetylcholine receptors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Additive effects of PDGF receptor beta signaling pathways in vascular smooth muscle cell development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Gene knockout of glycine transporter 1: characterization of the behavioral phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

High-throughput engineering of the mouse genome coupled with high-resolution expression analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Tools for targeted manipulation of the mouse genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Molecular determinants of atrial and ventricular septal defects and patent ductus arteriosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Synaptic assembly of the brain in the absence of neurotransmitter secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Neural tube closure and neural tube defects: studies in animal models reveal known knowns and known unknowns

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Clinical outcomes of congenital lung abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Impaired energy homeostasis in C/EBP alpha knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Genetic disruptions of O/E2 and O/E3 genes reveal involvement in olfactory receptor neuron projection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Forkhead transcription factor Foxf2 (LUN)-deficient mice exhibit abnormal development of secondary palate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Genetics of craniofacial development and malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Cysteine-rich domain isoforms of the neuregulin-1 gene are required for maintenance of peripheral synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

A role for Fyn tyrosine kinase in the suckling behaviour of neonatal mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Isolated cleft palate in mice with a targeted mutation of the LIM homeobox gene lhx8

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

Corticotropin-releasing hormone deficiency reveals major fetal but not adult glucocorticoid need

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00040.2007

10.1152/PHYSREV.00040.2007

21 January 2018

Identifiers

DOI

1 reference

19 August 2017

1 reference

PubMed ID

19126753