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Archives of Pharmacal Research
|
September 12, 2003
Compounds obtained from sida acuta with the potential to induce quinone reductase and to inhibit 7,12-dimethylbenz[a]anthracene-induced preneoplastic lesions in a mouse mammary organ culture model
Dae Sik Jang, Eun Jung Park, Young-Hwa Kang, et al.
Clinical Genetics
|
August 23, 2012
Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia
S G Mehta, M Khare, R Ramani, et al.
American Journal of Medical Genetics. Part A
|
February 9, 2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
Virginia E Kimonis, Sarju G Mehta, Erin C Fulchiero, et al.
Combinatorial Chemistry & High Throughput Screening
|
March 10, 2015
LiSIs: An Online Scientific Workflow System for Virtual Screening
Christos C Kannas, Ioanna Kalvari, George Lambrinidis, et al.
European Journal of Human Genetics : EJHG
|
January 28, 2010
Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci
Claire Louise Susan Turner, Deborah M Mackay, Jonathan L A Callaway, et al.
Human Molecular Genetics
|
March 24, 2016
Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity
Dragana J Josifova, Glen R Monroe, Federico Tessadori, et al.
American Journal of Human Genetics
|
December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5D
Margaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
HGG Advances
|
March 24, 2022
Biallelic variants in <i>TAMM41</i> are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease
Kyle Thompson, Lucas Bianchi, Francesca Rastelli, et al.
American Journal of Medical Genetics. Part A
|
July 18, 2019
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new cases
Lucy Bownass, Stephen Abbs, Ruth Armstrong, et al.
Clinical Genetics
|
April 9, 2026
Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome
Amber S E van Oirsouw, Tzung-Chien Hsieh, Martijn Koetsier, et al.
Page
of 41
Search research articles
Search
Showing results (371-380 of 402) with videos related to
Sort By:
Page
of 41
Archives of Pharmacal Research
|
September 12, 2003
Compounds obtained from sida acuta with the potential to induce quinone reductase and to inhibit 7,12-dimethylbenz[a]anthracene-induced preneoplastic lesions in a mouse mammary organ culture model
Dae Sik Jang, Eun Jung Park, Young-Hwa Kang, et al.
Clinical Genetics
|
August 23, 2012
Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia
S G Mehta, M Khare, R Ramani, et al.
American Journal of Medical Genetics. Part A
|
February 9, 2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
Virginia E Kimonis, Sarju G Mehta, Erin C Fulchiero, et al.
Combinatorial Chemistry & High Throughput Screening
|
March 10, 2015
LiSIs: An Online Scientific Workflow System for Virtual Screening
Christos C Kannas, Ioanna Kalvari, George Lambrinidis, et al.
European Journal of Human Genetics : EJHG
|
January 28, 2010
Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci
Claire Louise Susan Turner, Deborah M Mackay, Jonathan L A Callaway, et al.
Human Molecular Genetics
|
March 24, 2016
Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity
Dragana J Josifova, Glen R Monroe, Federico Tessadori, et al.
American Journal of Human Genetics
|
December 25, 2012
Mutations in ECEL1 cause distal arthrogryposis type 5D
Margaret J McMillin, Jennifer E Below, Kathryn M Shively, et al.
HGG Advances
|
March 24, 2022
Biallelic variants in <i>TAMM41</i> are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease
Kyle Thompson, Lucas Bianchi, Francesca Rastelli, et al.
American Journal of Medical Genetics. Part A
|
July 18, 2019
PAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new cases
Lucy Bownass, Stephen Abbs, Ruth Armstrong, et al.
Clinical Genetics
|
April 9, 2026
Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome
Amber S E van Oirsouw, Tzung-Chien Hsieh, Martijn Koetsier, et al.
Page
of 41