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Human Genetics
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August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1
Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
NPJ Breast Cancer
|
February 7, 2026
Constitutional BRCA1 Methylation is associated with high level of tumoral BRCA1 methylation and homologous recombination deficiency in triple-negative breast cancer
Justine Pasanisi, Constance Lamy, Lolita Lecompte, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 13, 2021
Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant
Thomas Huby, Edouard Le Guillou, Cyril Burin des Roziers, et al.
Orphanet Journal of Rare Diseases
|
February 5, 2025
The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update
Lucas Bouys, Anna Vaczlavik, Isadora P Cavalcante, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 13, 2013
The activation of the WNT signaling pathway is a Hallmark in neurofibromatosis type 1 tumorigenesis
Armelle Luscan, Ghjuvan'ghjacumu Shackleford, Julien Masliah-Planchon, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
October 25, 2025
Expanding the Clinicopathologic Spectrum of EWSR1::SSX-Rearranged Sarcomas: Series of 11 Cases Including Osteosarcomas and a Novel EWSR1::SSX4 Fusion
John M Gross, David I Suster, Ying Zou, et al.
Genes & Development
|
December 6, 2015
Impaired PRC2 activity promotes transcriptional instability and favors breast tumorigenesis
Michel Wassef, Veronica Rodilla, Aurélie Teissandier, et al.
European Journal of Endocrinology
|
March 10, 2022
Transcriptome in paraffin samples for the diagnosis and prognosis of adrenocortical carcinoma
Anne Jouinot, Juliane Lippert, Mathilde Sibony, et al.
Cancer Medicine
|
June 15, 2019
NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomas
Camille Tlemsani, Nicolas Pécuchet, Aurelia Gruber, et al.
Human Mutation
|
June 1, 2010
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype
Eric Pasmant, Audrey Sabbagh, Gill Spurlock, et al.
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of 13
Search research articles
Search
Showing results (101-110 of 124) with videos related to
Sort By:
Page
of 13
Human Genetics
|
August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1
Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
NPJ Breast Cancer
|
February 7, 2026
Constitutional BRCA1 Methylation is associated with high level of tumoral BRCA1 methylation and homologous recombination deficiency in triple-negative breast cancer
Justine Pasanisi, Constance Lamy, Lolita Lecompte, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 13, 2021
Noninvasive Prenatal Diagnosis of a Paternally Inherited MEN1 Pathogenic Splicing Variant
Thomas Huby, Edouard Le Guillou, Cyril Burin des Roziers, et al.
Orphanet Journal of Rare Diseases
|
February 5, 2025
The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update
Lucas Bouys, Anna Vaczlavik, Isadora P Cavalcante, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 13, 2013
The activation of the WNT signaling pathway is a Hallmark in neurofibromatosis type 1 tumorigenesis
Armelle Luscan, Ghjuvan'ghjacumu Shackleford, Julien Masliah-Planchon, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
October 25, 2025
Expanding the Clinicopathologic Spectrum of EWSR1::SSX-Rearranged Sarcomas: Series of 11 Cases Including Osteosarcomas and a Novel EWSR1::SSX4 Fusion
John M Gross, David I Suster, Ying Zou, et al.
Genes & Development
|
December 6, 2015
Impaired PRC2 activity promotes transcriptional instability and favors breast tumorigenesis
Michel Wassef, Veronica Rodilla, Aurélie Teissandier, et al.
European Journal of Endocrinology
|
March 10, 2022
Transcriptome in paraffin samples for the diagnosis and prognosis of adrenocortical carcinoma
Anne Jouinot, Juliane Lippert, Mathilde Sibony, et al.
Cancer Medicine
|
June 15, 2019
NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomas
Camille Tlemsani, Nicolas Pécuchet, Aurelia Gruber, et al.
Human Mutation
|
June 1, 2010
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype
Eric Pasmant, Audrey Sabbagh, Gill Spurlock, et al.
Page
of 13