Search research articles
Contact Us
Filters
Showing results (71-80 of 241) with videos related to
Page
of 25
Sort By:
The FEBS Journal
|
November 13, 2019
Direct regulation of Chk1 protein stability by E3 ubiquitin ligase HUWE1
Katelyn B Cassidy, Scott Bang, Manabu Kurokawa, et al.
Journal of Molecular Biology
|
March 25, 1984
Characterization of rat ribosomal DNA. The highly repetitive sequences that flank the ribosomal RNA transcription unit are homologous and contain RNA polymerase III transcription initiation sites
D L Mroczka, B Cassidy, H Busch, et al.
Nucleic Acids Research
|
June 25, 1982
Nucleotide sequence of the region between the 18S rRNA sequence and the 28S rRNA sequence of rat ribosomal DNA
C S Subrahmanyam, B Cassidy, H Busch, et al.
American Journal of Medical Genetics
|
July 11, 1997
Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15
M Gunay-Aygun, S Heeger, S Schwartz, et al.
The Journal of Investigative Dermatology
|
November 17, 2015
Beyond Red Hair and Sunburns: Uncovering the Molecular Mechanisms of MC1R Signaling and Repair of UV-Induced DNA Damage
Pamela B Cassidy, Zalfa A Abdel-Malek, Sancy A Leachman
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 7, 2007
Nutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype
P Galassetti, O Saetrum Opgaard, S B Cassidy, et al.
Journal of Child Neurology
|
March 1, 1996
Respiratory sinus arrhythmia in patients with Prader-Willi syndrome
F J DiMario, L Bauer, J Volpe, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2018
Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome
June-Anne Gold, Ranim Mahmoud, Suzanne B Cassidy, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 26, 2001
Selenazolidines as novel organoselenium delivery agents
Y Xie, M D Short, P B Cassidy, et al.
American Journal of Mental Deficiency
|
January 1, 1976
Chromosome 11 long arm partial deletion: a new syndrome
E Engel, C S Hirshberg, S B Cassidy, et al.
Page
of 25
Search research articles
Search
Showing results (71-80 of 241) with videos related to
Sort By:
Page
of 25
The FEBS Journal
|
November 13, 2019
Direct regulation of Chk1 protein stability by E3 ubiquitin ligase HUWE1
Katelyn B Cassidy, Scott Bang, Manabu Kurokawa, et al.
Journal of Molecular Biology
|
March 25, 1984
Characterization of rat ribosomal DNA. The highly repetitive sequences that flank the ribosomal RNA transcription unit are homologous and contain RNA polymerase III transcription initiation sites
D L Mroczka, B Cassidy, H Busch, et al.
Nucleic Acids Research
|
June 25, 1982
Nucleotide sequence of the region between the 18S rRNA sequence and the 28S rRNA sequence of rat ribosomal DNA
C S Subrahmanyam, B Cassidy, H Busch, et al.
American Journal of Medical Genetics
|
July 11, 1997
Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15
M Gunay-Aygun, S Heeger, S Schwartz, et al.
The Journal of Investigative Dermatology
|
November 17, 2015
Beyond Red Hair and Sunburns: Uncovering the Molecular Mechanisms of MC1R Signaling and Repair of UV-Induced DNA Damage
Pamela B Cassidy, Zalfa A Abdel-Malek, Sancy A Leachman
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 7, 2007
Nutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype
P Galassetti, O Saetrum Opgaard, S B Cassidy, et al.
Journal of Child Neurology
|
March 1, 1996
Respiratory sinus arrhythmia in patients with Prader-Willi syndrome
F J DiMario, L Bauer, J Volpe, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2018
Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome
June-Anne Gold, Ranim Mahmoud, Suzanne B Cassidy, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 26, 2001
Selenazolidines as novel organoselenium delivery agents
Y Xie, M D Short, P B Cassidy, et al.
American Journal of Mental Deficiency
|
January 1, 1976
Chromosome 11 long arm partial deletion: a new syndrome
E Engel, C S Hirshberg, S B Cassidy, et al.
Page
of 25