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American Journal of Medical Genetics. Part A
|
January 11, 2016
Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome
Brian T Wilson, Anneline Lochan, Zornitza Stark, et al.
Pediatrics
|
August 26, 2015
Metronidazole Toxicity in Cockayne Syndrome: A Case Series
Brian T Wilson, Andrew Strong, Sean O'Kelly, et al.
American Journal of Medical Genetics. Part A
|
June 25, 2013
Juvenile idiopathic arthritis, mitral valve prolapse and a familial variant involving the integrin-binding fragment of FBN1
Brian T Wilson, Sacha A Jensen, Ciaron P McAnulty, et al.
Clinical Dysmorphology
|
November 24, 2011
A case of mosaic trisomy 19q12-q13.2 with high BMI, macrocephaly, and speech delay: does USF2 determine size in the 19q phenotypes?
Brian T Wilson, Rachel Newby, Kathryn Watts, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2015
Microdeletion 1p35.2: a recognizable facial phenotype with developmental delay
Brian T Wilson, Murwan Omer, Stephen W Hellens, et al.
Oncotarget
|
May 3, 2017
Functional characterisation of a novel ovarian cancer cell line, NUOC-1
Aiste McCormick, Eleanor Earp, Katherine Elliot, et al.
Ebiomedicine
|
July 19, 2016
Glycosylation is an Androgen-Regulated Process Essential for Prostate Cancer Cell Viability
Jennifer Munkley, Daniel Vodak, Karen E Livermore, et al.
Oncotarget
|
October 10, 2015
The androgen receptor controls expression of the cancer-associated sTn antigen and cell adhesion through induction of ST6GalNAc1 in prostate cancer
Jennifer Munkley, Sebastian Oltean, Daniel Vodák, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2015
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care
Brian T Wilson, Zornitza Stark, Ruth E Sutton, et al.
The Journal of Experimental Medicine
|
December 14, 2020
ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients
Katja Apelt, Susan M White, Hyun Suk Kim, et al.
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of 2
Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics. Part A
|
January 11, 2016
Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome
Brian T Wilson, Anneline Lochan, Zornitza Stark, et al.
Pediatrics
|
August 26, 2015
Metronidazole Toxicity in Cockayne Syndrome: A Case Series
Brian T Wilson, Andrew Strong, Sean O'Kelly, et al.
American Journal of Medical Genetics. Part A
|
June 25, 2013
Juvenile idiopathic arthritis, mitral valve prolapse and a familial variant involving the integrin-binding fragment of FBN1
Brian T Wilson, Sacha A Jensen, Ciaron P McAnulty, et al.
Clinical Dysmorphology
|
November 24, 2011
A case of mosaic trisomy 19q12-q13.2 with high BMI, macrocephaly, and speech delay: does USF2 determine size in the 19q phenotypes?
Brian T Wilson, Rachel Newby, Kathryn Watts, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2015
Microdeletion 1p35.2: a recognizable facial phenotype with developmental delay
Brian T Wilson, Murwan Omer, Stephen W Hellens, et al.
Oncotarget
|
May 3, 2017
Functional characterisation of a novel ovarian cancer cell line, NUOC-1
Aiste McCormick, Eleanor Earp, Katherine Elliot, et al.
Ebiomedicine
|
July 19, 2016
Glycosylation is an Androgen-Regulated Process Essential for Prostate Cancer Cell Viability
Jennifer Munkley, Daniel Vodak, Karen E Livermore, et al.
Oncotarget
|
October 10, 2015
The androgen receptor controls expression of the cancer-associated sTn antigen and cell adhesion through induction of ST6GalNAc1 in prostate cancer
Jennifer Munkley, Sebastian Oltean, Daniel Vodák, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2015
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care
Brian T Wilson, Zornitza Stark, Ruth E Sutton, et al.
The Journal of Experimental Medicine
|
December 14, 2020
ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients
Katja Apelt, Susan M White, Hyun Suk Kim, et al.
Page
of 2