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Clinical Genetics
|
May 1, 1992
Lethal congenital erythroderma: a newly recognised genetic disorder
J P Shield, M R Judge, W Reardon, et al.
Clinical and Experimental Dermatology
|
September 3, 2003
Mycosis fungoides involving the oral mucosa in a child
E M Wain, J Setterfield, M R Judge, et al.
Journal of the American College of Surgeons
|
February 2, 2023
Low Muscle Mass and Radiodensity Associate with Impaired Pulmonary Function and Respiratory Complications in Patients with Esophageal Cancer
Miles E Cameron, Alexander L Ayzengart, Olusola Oduntan, et al.
Polymer Science & Technology (Washington, D.C.)
|
June 8, 2026
Bio-Based Self-Curing Phthalonitrile Resins Derived from Cinnamaldehyde
Loren C Brown, Giuliana R Judge, Cole R Davis, et al.
Journal of Muscle Research and Cell Motility
|
July 28, 2018
Cold shock protein RBM3 attenuates atrophy and induces hypertrophy in skeletal muscle
Douglas W Van Pelt, Amy L Confides, Andrew R Judge, et al.
The Journal of Investigative Dermatology
|
July 1, 1992
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)
A Ishida-Yamamoto, J A McGrath, M R Judge, et al.
Contact Dermatitis
|
February 1, 1996
Variation in response of human skin to irritant challenge
M R Judge, H A Griffiths, D A Basketter, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
October 27, 2018
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
Daryl P Fields, Brandon M Roberts, Alec K Simon, et al.
Plos One
|
August 25, 2015
Identification of the Acetylation and Ubiquitin-Modified Proteome during the Progression of Skeletal Muscle Atrophy
Daniel J Ryder, Sarah M Judge, Adam W Beharry, et al.
Journal of Cell Science
|
January 28, 2014
HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy
Adam W Beharry, Pooja B Sandesara, Brandon M Roberts, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 166) with videos related to
Sort By:
Page
of 17
Clinical Genetics
|
May 1, 1992
Lethal congenital erythroderma: a newly recognised genetic disorder
J P Shield, M R Judge, W Reardon, et al.
Clinical and Experimental Dermatology
|
September 3, 2003
Mycosis fungoides involving the oral mucosa in a child
E M Wain, J Setterfield, M R Judge, et al.
Journal of the American College of Surgeons
|
February 2, 2023
Low Muscle Mass and Radiodensity Associate with Impaired Pulmonary Function and Respiratory Complications in Patients with Esophageal Cancer
Miles E Cameron, Alexander L Ayzengart, Olusola Oduntan, et al.
Polymer Science & Technology (Washington, D.C.)
|
June 8, 2026
Bio-Based Self-Curing Phthalonitrile Resins Derived from Cinnamaldehyde
Loren C Brown, Giuliana R Judge, Cole R Davis, et al.
Journal of Muscle Research and Cell Motility
|
July 28, 2018
Cold shock protein RBM3 attenuates atrophy and induces hypertrophy in skeletal muscle
Douglas W Van Pelt, Amy L Confides, Andrew R Judge, et al.
The Journal of Investigative Dermatology
|
July 1, 1992
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)
A Ishida-Yamamoto, J A McGrath, M R Judge, et al.
Contact Dermatitis
|
February 1, 1996
Variation in response of human skin to irritant challenge
M R Judge, H A Griffiths, D A Basketter, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
October 27, 2018
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
Daryl P Fields, Brandon M Roberts, Alec K Simon, et al.
Plos One
|
August 25, 2015
Identification of the Acetylation and Ubiquitin-Modified Proteome during the Progression of Skeletal Muscle Atrophy
Daniel J Ryder, Sarah M Judge, Adam W Beharry, et al.
Journal of Cell Science
|
January 28, 2014
HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy
Adam W Beharry, Pooja B Sandesara, Brandon M Roberts, et al.
Page
of 17