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The Journal of Clinical Endocrinology and Metabolism
|
January 8, 2013
Bioinactive ACTH causing glucocorticoid deficiency
Mark E Samuels, Nicole Gallo-Payet, Sandra Pinard, et al.
Human Mutation
|
October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxia
Sarah L Sawyer, Jeremy Schwartzentruber, Chandree L Beaulieu, et al.
Genes
|
January 23, 2024
The Mutational Spectrum of Pre- and Post-Neoadjuvant Chemotherapy Triple-Negative Breast Cancers
Adriana Aguilar-Mahecha, Najmeh Alirezaie, Josiane Lafleur, et al.
Cell Reports
|
February 2, 2024
H2A.Z histone variants facilitate HDACi-dependent removal of H3.3K27M mutant protein in pediatric high-grade glioma cells
Katarzyna B Leszczynska, Amanda Freitas-Huhtamäki, Chinchu Jayaprakash, et al.
Plos Genetics
|
August 15, 2009
Tissue effect on genetic control of transcript isoform variation
Tony Kwan, Elin Grundberg, Vonda Koka, et al.
The Journal of Pathology
|
June 19, 2013
Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back again
Leora Witkowski, Emilie Lalonde, Jian Zhang, et al.
Scientific Reports
|
September 8, 2020
Prognostic and predictive value of circulating tumor DNA during neoadjuvant chemotherapy for triple negative breast cancer
Luca Cavallone, Adriana Aguilar-Mahecha, Josiane Lafleur, et al.
BMC Medical Genomics
|
October 29, 2011
Identification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell lines
Kevin C H Ha, Emilie Lalonde, Lili Li, et al.
Plos Pathogens
|
September 27, 2013
Genome-wide mouse mutagenesis reveals CD45-mediated T cell function as critical in protective immunity to HSV-1
Grégory Caignard, Gabriel A Leiva-Torres, Michael Leney-Greene, et al.
Journal of Medical Genetics
|
September 27, 2012
Mutations in TMEM231 cause Joubert syndrome in French Canadians
Myriam Srour, Fadi F Hamdan, Jeremy A Schwartzentruber, et al.
Page
of 34
Search research articles
Search
Showing results (231-240 of 333) with videos related to
Sort By:
Page
of 34
The Journal of Clinical Endocrinology and Metabolism
|
January 8, 2013
Bioinactive ACTH causing glucocorticoid deficiency
Mark E Samuels, Nicole Gallo-Payet, Sandra Pinard, et al.
Human Mutation
|
October 11, 2013
Exome sequencing as a diagnostic tool for pediatric-onset ataxia
Sarah L Sawyer, Jeremy Schwartzentruber, Chandree L Beaulieu, et al.
Genes
|
January 23, 2024
The Mutational Spectrum of Pre- and Post-Neoadjuvant Chemotherapy Triple-Negative Breast Cancers
Adriana Aguilar-Mahecha, Najmeh Alirezaie, Josiane Lafleur, et al.
Cell Reports
|
February 2, 2024
H2A.Z histone variants facilitate HDACi-dependent removal of H3.3K27M mutant protein in pediatric high-grade glioma cells
Katarzyna B Leszczynska, Amanda Freitas-Huhtamäki, Chinchu Jayaprakash, et al.
Plos Genetics
|
August 15, 2009
Tissue effect on genetic control of transcript isoform variation
Tony Kwan, Elin Grundberg, Vonda Koka, et al.
The Journal of Pathology
|
June 19, 2013
Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back again
Leora Witkowski, Emilie Lalonde, Jian Zhang, et al.
Scientific Reports
|
September 8, 2020
Prognostic and predictive value of circulating tumor DNA during neoadjuvant chemotherapy for triple negative breast cancer
Luca Cavallone, Adriana Aguilar-Mahecha, Josiane Lafleur, et al.
BMC Medical Genomics
|
October 29, 2011
Identification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell lines
Kevin C H Ha, Emilie Lalonde, Lili Li, et al.
Plos Pathogens
|
September 27, 2013
Genome-wide mouse mutagenesis reveals CD45-mediated T cell function as critical in protective immunity to HSV-1
Grégory Caignard, Gabriel A Leiva-Torres, Michael Leney-Greene, et al.
Journal of Medical Genetics
|
September 27, 2012
Mutations in TMEM231 cause Joubert syndrome in French Canadians
Myriam Srour, Fadi F Hamdan, Jeremy A Schwartzentruber, et al.
Page
of 34