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528601 to 528700 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly.
THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY).
Cdc42 deficiency causes Sonic hedgehog-independent holoprosencephaly.
Chordin and noggin promote organizing centers of forebrain development in the mouse.
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
Inhibition of sonic hedgehog signaling in vivo results in craniofacial neural crest cell death.
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Genetics of ventral forebrain development and holoprosencephaly.
Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes.
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
Cdo functions at multiple points in the Sonic Hedgehog pathway, and Cdo-deficient mice accurately model human holoprosencephaly.
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
Smad5 knockout mice die at mid-gestation due to multiple embryonic and extraembryonic defects.
Defective forebrain development in mice lacking gp330/megalin.
Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches.
Requirement for the lpA1 lysophosphatidic acid receptor gene in normal suckling behavior.
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
Bright Yellow Urine, Folic Acid Deficiency, flatulence, abdominal pain, eruptions, chronic pain, focal, skin pustule, pruritus
Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice.
Smad2 role in mesoderm formation, left-right patterning and craniofacial development.
Function of Rieger syndrome gene in left-right asymmetry and craniofacial development.
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome.
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development.
An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis.
Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development.
p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development.
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.
Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.
Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.
Cleft lip and palate: understanding genetic and environmental influences.
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
Cleft palate and decreased brain gamma-aminobutyric acid in mice lacking the 67-kDa isoform of glutamic acid decarboxylase.
Rescue of cleft palate in Msx1-deficient mice by transgenic Bmp4 reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis.
Gene/environment causes of cleft lip and/or palate.
Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects.
back pain ankle clonus, chronic pain
Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.
Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.
Recent advances in craniofacial morphogenesis.
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development.
Transforming growth factor-beta 3 is required for secondary palate fusion.
Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction.
A 5-year retrospective study of zygomatico-orbital complex and zygomatic arch fractures in Sao Paulo State, Brazil.
Zygomatic fractures: comparison of methods of internal fixation.
Resorbable poly(L-lactide) plates and screws for the fixation of zygomatic fractures.
Bradycardia and the trigeminal nerve.
Trends in the characteristics of maxillofacial fractures in Nigeria.
Midface fractures: advantages of immediate extended open reduction and bone grafting.
Classification of potential risk factors for trigeminocardiac reflex in craniomaxillofacial surgery.
Foreign body reactions to resorbable poly(L-lactide) bone plates and screws used for the fixation of unstable zygomatic fractures.
Late degradation tissue response to poly(L-lactide) bone plates and screws.
Current concepts on the management of orbital blow-out fractures.
Blow-out fracture of the orbit; mechanism and correction of internal orbital fracture.
Air bag-associated ocular trauma in children.
Transcaruncular approach to the medial orbit and orbital apex.
CT of orbital trauma.
Clinical recommendations for repair of orbital facial fractures.
Bone marrow stromal cells with a combined expression of BMP-2 and VEGF-165 enhanced bone regeneration.
Airbag-associated ocular injury and periorbital fractures.
Surgery on orbital floor fractures. Influence of time of repair and fracture size.
Studies on enophthalmos: II. The measurement of orbital injuries and their treatment by quantitative computed tomography.
Ocular trauma in the United States. Eye injuries resulting in hospitalization, 1984 through 1987.
Mechanisms of global support and posttraumatic enophthalmos: I. The anatomy of the ligament sling and its relation to intramuscular cone orbital fat.
Eye injuries in childhood.
J E Burkhart
The importance of the zygomatic arch in complex midfacial fracture repair and correction of posttraumatic orbitozygomatic deformities.
Eyelid and orbital fascial attachments and their clinical significance.
Epidemiological analysis of maxillofacial fractures in Brazil: a 5-year prospective study.
Thoracolumbar "burst" fractures treated conservatively: a long-term follow-up.
AIDS commentary. Toxoplasmic encephalitis.
Recent expansion of Toxoplasma through enhanced oral transmission.
Kiss and spit: the dual roles of Toxoplasma rhoptries.
Toxoplasma gondii: transmission, diagnosis and prevention.
back pain ankle clonus
CD40 induces macrophage anti-Toxoplasma gondii activity by triggering autophagy-dependent fusion of pathogen-containing vacuoles and lysosomes.
Direct and sensitive detection of a pathogenic protozoan, Toxoplasma gondii, by polymerase chain reaction.
Failure to trigger the oxidative metabolic burst by normal macrophages: possible mechanism for survival of intracellular pathogens.
Structures of Toxoplasma gondii tachyzoites, bradyzoites, and sporozoites and biology and development of tissue cysts.
Autophagosome-independent essential function for the autophagy protein Atg5 in cellular immunity to intracellular pathogens.
The IL-27R (WSX-1) is required to suppress T cell hyperactivity during infection.
Regulation and function of T-cell-mediated immunity during Toxoplasma gondii infection.
T(H)1 cells control themselves by producing interleukin-10.
The definition of HIV-associated neurocognitive disorders: are we overestimating the real prevalence?
Decrease of Foxp3+ Treg cell number and acquisition of effector cell phenotype during lethal infection.
Impact of coronary artery calcium scanning on coronary risk factors and downstream testing the EISNER (Early Identification of Subclinical Atherosclerosis by Noninvasive Imaging Research) prospective randomized trial.
Conventional T-bet(+)Foxp3(-) Th1 cells are the major source of host-protective regulatory IL-10 during intracellular protozoan infection.
Toxoplasma gondii comprises three clonal lineages: correlation of parasite genotype with human disease.
Bartonella spp.: throwing light on uncommon human infections.
Bright Yellow Urine, Folic Acid Deficiency, flatulence, abdominal pain, eruptions, chronic pain, focal, skin pustule