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Full Text Induced GnasR201H expression from the endogenous Gnas locuscausesfibrous dysplasia
mutations in the Gs - alpha protein(passive) is caused byFibrous dysplasia
mutation in the mTOR regulator NPRL3(passive) caused bycortical dysplasia
a genetic mutation and is not inherited(passive) is caused byFibrous dysplasia
PreventionThere ... no known wayto preventfibrous dysplasia
the sporadic mutation of the GNAS1 gene , which encodes the alpha subunit of the stimulatory G protein ( G1 ) located on chromosome 20q13.2 - 13.3 of the osteoblastic cells(passive) is caused byFibrous dysplasia
a genetic mutation in a gene called the EphrinB1 ( EFNB1 ) gene on the X chromosome(passive) is caused byCraniofrontonasal dysplasia
frontonasal dysplasia - caused by mutations in the ALX4 gene At least four mutations in the ALX4 gene have been foundto causefrontonasal dysplasia
recurrent fracturesresultingfrom polyostotic fibrous dysplasia
a gene defect ( mutation ) that affects the cells that produce bone(passive) is caused byFibrous dysplasia
a somatic mutation in the GNAS1 gene on chromosome 20q13.2 - 13.3(passive) is caused byfibrous dysplasia
a spontaneous genetic mutation in the cells that produce bone(passive) is caused byFibrous dysplasia
McCune Albright Syndrome since birth , where abnormal tissue and cysts form in and around her bones(passive) caused bypolyostotic fibrous dysplasia
the pathological mechanismcausingcortical dysplasia
1–9 ] Lineage Determination of Chondrocytes and Osteoblasts : From the Perspective of Cellular and Molecular Biology Induced Gnas(R201H ) expression from the endogenous Gnas locuscausesfibrous dysplasia
mTOR activation in dorsal telencephalic progenitors , in some cases specifically the excitatory neuron lineagecausescortical dysplasia
mTOR activation in dorsal telencephalic progenitors , in some cases specifically the exictatory neuron lineagecausescortical dysplasia
McCune Albright Syndrome since birth , where abnormal tissue and cysts form in and around Sofia Jingsäter 's bones(passive) caused bypolyostotic fibrous dysplasia
TRPV4 mutations Thanatophoric Dysplasia ( TD(passive) are caused byparastremmatic dysplasia
TRPV4 mutations ( pages 1443–1449(passive) are caused byparastremmatic dysplasia
a mutation in a family of genes(passive) is caused byFrontonasal dysplasia
a somatic mutation in the GNAS1 gene located on chromosome 20q13.2 - 13.3 , which encodes the alpha subunit of the stimulatory G protein , Gsα(passive) is caused byFibrous dysplasia
A 15-year - old male with McCune - Albright syndrome wasadmitted with complaint of right nasal obstructionoriginatedfrom fibrous dysplasia
PubMed ] Mimura , N. ; Yuasa , S. ; Soma , M. ; Jin , H. ; Kimura , K. ; Goto , S. ; Koseki , H. ; Aoe , T. Altered quality control in the endoplasmic reticulumcausescortical dysplasia
mutations in the TRPV4 gene , which provides instructions for making a protein that acts as a calcium channel(passive) is caused byMetatropic dysplasia
a somatic activating mutation of the Gs alpha subunit of protein G ... resulting in an increased cAMP concentration and thus in abnormalities of osteoblast differentiation , these osteoblasts producing abnormal bone(passive) is caused byfibrous dysplasia
Mutation in a larger cell massmay resultin polyostotic fibrous dysplasia
a mutation in the gene called GNAS1(passive) is caused byFibrous dysplasia
a mutation in the gene dubbed as GNAS1(passive) is caused byfibrous dysplasia
View at Google Scholar Naoya Mimura , Shigeki Yuasa , Miho Soma , Hisayo Jin , Keita Kimura , Shigemasa Goto , Haruhiko Koseki , and Tomohiko Aoe , “ Altered quality control in the endoplasmic reticulumcausescortical dysplasia
a change ( mutation ... in a gene known as COL2A1(passive) is caused byDiscussionKniest dysplasia
a mutation ( or change ) in a gene called TRPV4 , which plays a role in cartilage and bone development(passive) is caused byMetatropic dysplasia
Yang Y. Induced expression from the endogenous locuscausesfibrous dysplasia
a mutation in the alpha subunit of stimulatory G protein(passive) is caused byFibrous dysplasia
a mutation in the GS alpha protein , which increases cAMP(passive) is caused byFibrous dysplasia
a mutation in a gene that codes for the cells that produce bone(passive) is caused byFibrous dysplasia
TRPV4 mutations AU - Bedeschi , Francesca AU - Schmidt - Rimpler , Maren AU - Spranger(passive) are caused byparastremmatic dysplasia
a mutation in a gene coding for a protein called G - protein(passive) is caused byFibrous dysplasia
an activating mutation of the same gene that actually causes Progressive osseous heteroplasia ( POH(passive) is caused byFibrous dysplasia
abnormal brain folding or cellular migration during fetal brain development(passive) caused bycortical dysplasia (
incidentally and with no signs or symptomsdiscoveredincidentally and with no signs or symptoms
abnormal growth or swelling of bone , Learning objectivescausesabnormal growth or swelling of bone , Learning objectives
no symptoms , mild symptoms , or severe symptoms.[3][4may causeno symptoms , mild symptoms , or severe symptoms.[3][4
little or no signs and symptomsmay causelittle or no signs and symptoms
abnormal growth or swelling of bone , cycling shoes heel protectorcausesabnormal growth or swelling of bone , cycling shoes heel protector
to your affected bone or bonesmay leadto your affected bone or bones
few or no signs or symptoms ... especially if it is mildcausesfew or no signs or symptoms ... especially if it is mild
Basavaraju L. An unusual presentation of trigeminal neuralgia(passive) caused byBasavaraju L. An unusual presentation of trigeminal neuralgia
few or no signs and symptoms ... particularly if the condition is mildmay causefew or no signs and symptoms ... particularly if the condition is mild
incidentally and have n’t experienced any signs or symptomsdiscoveredincidentally and have n’t experienced any signs or symptoms
bone lesions(passive) caused bybone lesions
your affected bone to become deformedcan causeyour affected bone to become deformed
in intractable epilepsyresultingin intractable epilepsy
epilepsy ( Ropercausingepilepsy ( Roper
focal epilepsy(passive) caused byfocal epilepsy
to similar swellings in the metaphyseal areaalso leadto similar swellings in the metaphyseal area
epileptic seizures(passive) caused byepileptic seizures
bone pain and deformitiescausesbone pain and deformities
irregular progress or swelling of bonecausesirregular progress or swelling of bone
cranial nerve impingementcausescranial nerve impingement
hollow lesions in my bonescauseshollow lesions in my bones
no signs or symptoms carries a low risk of developing bone deformities or fracturing the bonecausesno signs or symptoms carries a low risk of developing bone deformities or fracturing the bone
extensive skull involvement(passive) caused byextensive skull involvement
Select item 158169751.Surgical outcome of epilepsy(passive) caused bySelect item 158169751.Surgical outcome of epilepsy
C Justin Lee Surgical outcome of epilepsy(passive) caused byC Justin Lee Surgical outcome of epilepsy
the affected bone to deform and become susceptible to fracturecan causethe affected bone to deform and become susceptible to fracture
12 Reversible visual loss(passive) caused by12 Reversible visual loss
medically refractory epilepsy(passive) caused bymedically refractory epilepsy
refractory epilepsy in childrencausingrefractory epilepsy in children
patients to suffer from epilepsy or seizures and brain retardationcausespatients to suffer from epilepsy or seizures and brain retardation
to seizures and developmental retardationcan leadto seizures and developmental retardation
in refractory partial seizuresmay resultin refractory partial seizures
their son 's seizures(passive) caused bytheir son 's seizures
complications such as pressure against the brain , spinal cord or nerves is also treated with surgerycausescomplications such as pressure against the brain , spinal cord or nerves is also treated with surgery
Vinters HV Reversible visual loss(passive) caused byVinters HV Reversible visual loss
244 - 249 Reversible visual loss(passive) caused by244 - 249 Reversible visual loss
3 4 23 54 Spondylo - epiphyseal dysplasia , Maroteaux type ( pseudo - Morquio syndrome type 2 ) , and(passive) are caused3 4 23 54 Spondylo - epiphyseal dysplasia , Maroteaux type ( pseudo - Morquio syndrome type 2 ) , and
in many symptoms , such as orbital dysplasia , diplopia , and proptosis.[17may resultin many symptoms , such as orbital dysplasia , diplopia , and proptosis.[17
a huge lesion on her face(passive) caused bya huge lesion on her face
to malignant change.[3leadingto malignant change.[3