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American Journal of Medical Genetics. Part A
|
August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features
Patricia G Wheeler, Bobby G Ng, Laura Sanford, et al.
Protein Science : a Publication of the Protein Society
|
July 23, 2020
Cumulative deamidations of the major lens protein γS-crystallin increase its aggregation during unfolding and oxidation
Calvin J Vetter, David C Thorn, Samuel G Wheeler, et al.
American Journal of Human Genetics
|
March 2, 2010
Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS
Feng Zhang, Lorraine Potocki, Jacinda B Sampson, et al.
The American Journal of Pathology
|
May 23, 2012
Ectonucleotide triphosphate diphosphohydrolase-1 (CD39) mediates resistance to occlusive arterial thrombus formation after vascular injury in mice
Zachary M Huttinger, Michael W Milks, Michael S Nickoli, et al.
Journal of Visualized Experiments : Jove
|
September 25, 2018
Ferric Chloride-induced Canine Carotid Artery Thrombosis: A Large Animal Model of Vascular Injury
Allyson L Huttinger, Debra G Wheeler, Surya Gnyawali, et al.
Journal of Neuro-Oncology
|
March 26, 2014
Expression of PRMT5 correlates with malignant grade in gliomas and plays a pivotal role in tumor growth in vitro
Xiaosi Han, Rong Li, Wenbin Zhang, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
February 22, 2011
Antioxidant network expression abrogates oxidative posttranslational modifications in mice
R Mital, W Zhang, M Cai, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))
|
November 1, 2020
Long-term Survival with 18-Fluorodeoxyglucose Positron Emission Tomography-directed Therapy in Non-small Cell Lung Cancer with Synchronous Solitary Brain Metastasis
S Newman, N Bucknell, M Bressel, et al.
Human Mutation
|
March 30, 2021
Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor
Bryn D Webb, Anthony Evans, Thomas P Naidich, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndrome
Karen W Gripp, Angela E Lin, Linda Nicholson, et al.
Page
of 39
Search research articles
Search
Showing results (331-340 of 383) with videos related to
Sort By:
Page
of 39
American Journal of Medical Genetics. Part A
|
August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features
Patricia G Wheeler, Bobby G Ng, Laura Sanford, et al.
Protein Science : a Publication of the Protein Society
|
July 23, 2020
Cumulative deamidations of the major lens protein γS-crystallin increase its aggregation during unfolding and oxidation
Calvin J Vetter, David C Thorn, Samuel G Wheeler, et al.
American Journal of Human Genetics
|
March 2, 2010
Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS
Feng Zhang, Lorraine Potocki, Jacinda B Sampson, et al.
The American Journal of Pathology
|
May 23, 2012
Ectonucleotide triphosphate diphosphohydrolase-1 (CD39) mediates resistance to occlusive arterial thrombus formation after vascular injury in mice
Zachary M Huttinger, Michael W Milks, Michael S Nickoli, et al.
Journal of Visualized Experiments : Jove
|
September 25, 2018
Ferric Chloride-induced Canine Carotid Artery Thrombosis: A Large Animal Model of Vascular Injury
Allyson L Huttinger, Debra G Wheeler, Surya Gnyawali, et al.
Journal of Neuro-Oncology
|
March 26, 2014
Expression of PRMT5 correlates with malignant grade in gliomas and plays a pivotal role in tumor growth in vitro
Xiaosi Han, Rong Li, Wenbin Zhang, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
February 22, 2011
Antioxidant network expression abrogates oxidative posttranslational modifications in mice
R Mital, W Zhang, M Cai, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))
|
November 1, 2020
Long-term Survival with 18-Fluorodeoxyglucose Positron Emission Tomography-directed Therapy in Non-small Cell Lung Cancer with Synchronous Solitary Brain Metastasis
S Newman, N Bucknell, M Bressel, et al.
Human Mutation
|
March 30, 2021
Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor
Bryn D Webb, Anthony Evans, Thomas P Naidich, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndrome
Karen W Gripp, Angela E Lin, Linda Nicholson, et al.
Page
of 39