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Miriam J Smith

Showing results (51-60 of 81) with videos related to

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Cancers|August 27, 2021
Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior <i>BRCA1/2</i> ProbabilityD Gareth Evans, Elke M van Veen, Emma R Woodward, et al.
JAMA Neurology|August 1, 2017
Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young AdultsOmar N Pathmanaban, Katherine V Sadler, Ian D Kamaly-Asl, et al.
American Journal of Human Genetics|September 11, 2012
Loss of SUFU function in familial multiple meningiomaMervi Aavikko, Song-Ping Li, Silva Saarinen, et al.
American Journal of Human Genetics|August 4, 2018
A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian CancerD Gareth R Evans, Elke M van Veen, Helen J Byers, et al.
Medicine|February 1, 2018
Pain correlates with germline mutation in schwannomatosisJustin T Jordan, Miriam J Smith, James A Walker, et al.
American Journal of Medical Genetics. Part A|March 26, 2019
From process to progress-2017 International Conference on Neurofibromatosis 1, Neurofibromatosis 2 and SchwannomatosisRosalie E Ferner, Annette Bakker, Ype Elgersma, et al.
Familial Cancer|March 25, 2021
Extended gene panel testing in lobular breast cancerElke M van Veen, D Gareth Evans, Elaine F Harkness, et al.
Journal of Medical Genetics|February 1, 2011
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onsetMiriam J Smith, Jenny E Higgs, Naomi L Bowers, et al.
Nature Genetics|June 10, 2022
SMARCE1 deficiency generates a targetable mSWI/SNF dependency in clear cell meningiomaRoodolph St Pierre, Clayton K Collings, Daniel D Samé Guerra, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.
Pageof 9

Showing results (51-60 of 81) with videos related to

Sort By:
Pageof 9
Cancers|August 27, 2021
Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior <i>BRCA1/2</i> ProbabilityD Gareth Evans, Elke M van Veen, Emma R Woodward, et al.
JAMA Neurology|August 1, 2017
Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young AdultsOmar N Pathmanaban, Katherine V Sadler, Ian D Kamaly-Asl, et al.
American Journal of Human Genetics|September 11, 2012
Loss of SUFU function in familial multiple meningiomaMervi Aavikko, Song-Ping Li, Silva Saarinen, et al.
American Journal of Human Genetics|August 4, 2018
A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian CancerD Gareth R Evans, Elke M van Veen, Helen J Byers, et al.
Medicine|February 1, 2018
Pain correlates with germline mutation in schwannomatosisJustin T Jordan, Miriam J Smith, James A Walker, et al.
American Journal of Medical Genetics. Part A|March 26, 2019
From process to progress-2017 International Conference on Neurofibromatosis 1, Neurofibromatosis 2 and SchwannomatosisRosalie E Ferner, Annette Bakker, Ype Elgersma, et al.
Familial Cancer|March 25, 2021
Extended gene panel testing in lobular breast cancerElke M van Veen, D Gareth Evans, Elaine F Harkness, et al.
Journal of Medical Genetics|February 1, 2011
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onsetMiriam J Smith, Jenny E Higgs, Naomi L Bowers, et al.
Nature Genetics|June 10, 2022
SMARCE1 deficiency generates a targetable mSWI/SNF dependency in clear cell meningiomaRoodolph St Pierre, Clayton K Collings, Daniel D Samé Guerra, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.
Pageof 9