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Nature Cancer
|
August 18, 2022
Single-cell analysis and functional characterization uncover the stem cell hierarchies and developmental origins of rhabdomyosarcoma
Yun Wei, Qian Qin, Chuan Yan, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
January 24, 2015
ST13 polymorphisms and their effect on exacerbations in steroid-treated asthmatic children and young adults
S J H Vijverberg, E S Koster, R Tavendale, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
December 21, 2016
Multiplex KRASG12/G13 mutation testing of unamplified cell-free DNA from the plasma of patients with advanced cancers using droplet digital polymerase chain reaction
F Janku, H J Huang, T Fujii, et al.
American Journal of Human Genetics
|
April 16, 2003
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
E E M Jaeger, K L Woodford-Richens, M Lockett, et al.
Cancer Research
|
November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome
D J Marsh, S Roth, K L Lunetta, et al.
Nature Genetics
|
May 1, 1996
Localization of the gene for Cowden disease to chromosome 10q22-23
M R Nelen, G W Padberg, E A Peeters, et al.
Journal of Medical Genetics
|
July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment
S C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Human Molecular Genetics
|
July 13, 1999
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
D J Marsh, J B Kum, K L Lunetta, et al.
Nature Communications
|
June 3, 2026
MYOD1 mutation drives cancer stem cell pathways and therapy-resistance in spindle cell/sclerosing rhabdomyosarcoma
Yun Wei, Luis Antonio Corchete Sánchez, Sabateeshan Mathavarajah, et al.
JAMA
|
November 20, 1996
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
C Eng, D Clayton, I Schuffenecker, et al.
Page
of 39
Search research articles
Search
Showing results (371-380 of 385) with videos related to
Sort By:
Page
of 39
Nature Cancer
|
August 18, 2022
Single-cell analysis and functional characterization uncover the stem cell hierarchies and developmental origins of rhabdomyosarcoma
Yun Wei, Qian Qin, Chuan Yan, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
January 24, 2015
ST13 polymorphisms and their effect on exacerbations in steroid-treated asthmatic children and young adults
S J H Vijverberg, E S Koster, R Tavendale, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
December 21, 2016
Multiplex KRASG12/G13 mutation testing of unamplified cell-free DNA from the plasma of patients with advanced cancers using droplet digital polymerase chain reaction
F Janku, H J Huang, T Fujii, et al.
American Journal of Human Genetics
|
April 16, 2003
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
E E M Jaeger, K L Woodford-Richens, M Lockett, et al.
Cancer Research
|
November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome
D J Marsh, S Roth, K L Lunetta, et al.
Nature Genetics
|
May 1, 1996
Localization of the gene for Cowden disease to chromosome 10q22-23
M R Nelen, G W Padberg, E A Peeters, et al.
Journal of Medical Genetics
|
July 9, 2009
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment
S C Sreenath Nagamani, F Zhang, O A Shchelochkov, et al.
Human Molecular Genetics
|
July 13, 1999
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
D J Marsh, J B Kum, K L Lunetta, et al.
Nature Communications
|
June 3, 2026
MYOD1 mutation drives cancer stem cell pathways and therapy-resistance in spindle cell/sclerosing rhabdomyosarcoma
Yun Wei, Luis Antonio Corchete Sánchez, Sabateeshan Mathavarajah, et al.
JAMA
|
November 20, 1996
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
C Eng, D Clayton, I Schuffenecker, et al.
Page
of 39