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Science (New York, N.Y.)
|
December 26, 2001
KLF6, a candidate tumor suppressor gene mutated in prostate cancer
G Narla, K E Heath, H L Reeves, et al.
European Journal of Medical Genetics
|
October 15, 2023
Characterization of three adults and an adolescent with Osteogenesis Imperfecta type VI and a novel founder SERPINF1 variant
André M Travessa, Patrícia Dias, Joana Rosmaninho-Salgado, et al.
Environmental Pollution (Barking, Essex : 1987)
|
November 13, 2009
Inter-laboratory exercise on steroid estrogens in aqueous samples
E Heath, T Kosjek, H R Andersen, et al.
Nature
|
October 31, 2024
Dynamic interface printing
Callum Vidler, Michael Halwes, Kirill Kolesnik, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 15, 2010
Clinical and molecular evaluation of SHOX/PAR1 duplications in Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS)
S Benito-Sanz, E Barroso, D Heine-Suñer, et al.
Leukemia
|
December 7, 2021
Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells
Elisabeth R Wilson, Nichole M Helton, Sharon E Heath, et al.
Small (Weinheim an Der Bergstrasse, Germany)
|
July 14, 2026
A Platform for the Actuation of Magnetically Labeled Skeletal Muscle Cells Using Dynamic Magnetic Stimulation
Tayná C Rodrigues, Anna-Lena Bauknecht, Anna Gioran, et al.
Nature Genetics
|
June 1, 1997
Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats
T J Aitman, T Gotoda, A L Evans, et al.
American Journal of Medical Genetics. Part A
|
June 28, 2020
Variable pulmonary manifestations in Chitayat syndrome: Six additional affected individuals
Aude-Annick Suter, Fernando Santos-Simarro, Pernille Mathiesen Toerring, et al.
American Journal of Human Genetics
|
October 9, 2001
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes
K E Heath, A Campos-Barros, A Toren, et al.
Page
of 44
Search research articles
Search
Showing results (351-360 of 431) with videos related to
Sort By:
Page
of 44
Science (New York, N.Y.)
|
December 26, 2001
KLF6, a candidate tumor suppressor gene mutated in prostate cancer
G Narla, K E Heath, H L Reeves, et al.
European Journal of Medical Genetics
|
October 15, 2023
Characterization of three adults and an adolescent with Osteogenesis Imperfecta type VI and a novel founder SERPINF1 variant
André M Travessa, Patrícia Dias, Joana Rosmaninho-Salgado, et al.
Environmental Pollution (Barking, Essex : 1987)
|
November 13, 2009
Inter-laboratory exercise on steroid estrogens in aqueous samples
E Heath, T Kosjek, H R Andersen, et al.
Nature
|
October 31, 2024
Dynamic interface printing
Callum Vidler, Michael Halwes, Kirill Kolesnik, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 15, 2010
Clinical and molecular evaluation of SHOX/PAR1 duplications in Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS)
S Benito-Sanz, E Barroso, D Heine-Suñer, et al.
Leukemia
|
December 7, 2021
Focal disruption of DNA methylation dynamics at enhancers in IDH-mutant AML cells
Elisabeth R Wilson, Nichole M Helton, Sharon E Heath, et al.
Small (Weinheim an Der Bergstrasse, Germany)
|
July 14, 2026
A Platform for the Actuation of Magnetically Labeled Skeletal Muscle Cells Using Dynamic Magnetic Stimulation
Tayná C Rodrigues, Anna-Lena Bauknecht, Anna Gioran, et al.
Nature Genetics
|
June 1, 1997
Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats
T J Aitman, T Gotoda, A L Evans, et al.
American Journal of Medical Genetics. Part A
|
June 28, 2020
Variable pulmonary manifestations in Chitayat syndrome: Six additional affected individuals
Aude-Annick Suter, Fernando Santos-Simarro, Pernille Mathiesen Toerring, et al.
American Journal of Human Genetics
|
October 9, 2001
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes
K E Heath, A Campos-Barros, A Toren, et al.
Page
of 44