Search research articles
Contact Us
Filters
Showing results (41-50 of 94) with videos related to
Page
of 10
Sort By:
Journal of Cell Science
|
June 10, 2011
Differential altered stability and transcriptional activity of ΔNp63 mutants in distinct ectodermal dysplasias
Gareth Browne, Rita Cipollone, Anna Maria Lena, et al.
The Journal of Allergy and Clinical Immunology
|
August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)
Harjit Dadi, Tyler A Jones, Daniele Merico, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder
Kate Tsiplova, Richard M Zur, Christian R Marshall, et al.
Plos Genetics
|
August 23, 2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways
Candice K Silversides, Anath C Lionel, Gregory Costain, et al.
Genome Medicine
|
December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
Chelsea Lowther, Daniele Merico, Gregory Costain, et al.
Oncotarget
|
July 9, 2016
Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network
Nardin Samuel, Gavin Wilson, Badr Id Said, et al.
American Journal of Medical Genetics. Part A
|
August 18, 2016
Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing
Muhammad Imran Naseer, Sameera Sogaty, Mahmood Rasool, et al.
Blood
|
February 6, 2023
Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier
Akira Shiraishi, Vedat Uygun, Nigel Sharfe, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 27, 2024
Utilization of next-generation sequencing to define the role of heterozygous <i>FOXN1</i> variants in immunodeficiency
Yehonatan Pasternak, Linda Vong, Daniele Merico, et al.
Science Translational Medicine
|
September 17, 2020
B cell acute lymphoblastic leukemia cells mediate RANK-RANKL-dependent bone destruction
Sujeetha A Rajakumar, Eniko Papp, Kathy K Lee, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 94) with videos related to
Sort By:
Page
of 10
Journal of Cell Science
|
June 10, 2011
Differential altered stability and transcriptional activity of ΔNp63 mutants in distinct ectodermal dysplasias
Gareth Browne, Rita Cipollone, Anna Maria Lena, et al.
The Journal of Allergy and Clinical Immunology
|
August 23, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)
Harjit Dadi, Tyler A Jones, Daniele Merico, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder
Kate Tsiplova, Richard M Zur, Christian R Marshall, et al.
Plos Genetics
|
August 23, 2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways
Candice K Silversides, Anath C Lionel, Gregory Costain, et al.
Genome Medicine
|
December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
Chelsea Lowther, Daniele Merico, Gregory Costain, et al.
Oncotarget
|
July 9, 2016
Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network
Nardin Samuel, Gavin Wilson, Badr Id Said, et al.
American Journal of Medical Genetics. Part A
|
August 18, 2016
Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing
Muhammad Imran Naseer, Sameera Sogaty, Mahmood Rasool, et al.
Blood
|
February 6, 2023
Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier
Akira Shiraishi, Vedat Uygun, Nigel Sharfe, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 27, 2024
Utilization of next-generation sequencing to define the role of heterozygous <i>FOXN1</i> variants in immunodeficiency
Yehonatan Pasternak, Linda Vong, Daniele Merico, et al.
Science Translational Medicine
|
September 17, 2020
B cell acute lymphoblastic leukemia cells mediate RANK-RANKL-dependent bone destruction
Sujeetha A Rajakumar, Eniko Papp, Kathy K Lee, et al.
Page
of 10