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Nature Communications
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January 28, 2017
Rhomboid family member 2 regulates cytoskeletal stress-associated Keratin 16
Thiviyani Maruthappu, Anissa Chikh, Benjamin Fell, et al.
Human Mutation
|
June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia
M Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
Cancer Genetics and Cytogenetics
|
November 19, 2003
Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability
N A Alam, P Gorman, E E M Jaeger, et al.
Journal of Cell Science
|
July 4, 2003
Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability
Andrew P South, Hong Wan, Michael G Stone, et al.
Journal of the National Cancer Institute
|
June 19, 1996
Human papillomavirus infections in nonmelanoma skin cancers from renal transplant recipients and nonimmunosuppressed patients
V Shamanin, H zur Hausen, D Lavergne, et al.
NPJ Precision Oncology
|
September 2, 2025
Enhanced metastasis risk prediction in cutaneous squamous cell carcinoma using deep learning and computational histopathology
Emilia Peleva, Yue Chen, Bernhard Finke, et al.
The British Journal of Dermatology
|
March 14, 2019
Epidemiology of basal and cutaneous squamous cell carcinoma in the U.K. 2013-15: a cohort study
Z C Venables, T Nijsten, K F Wong, et al.
Oncogene
|
September 6, 2002
Characterization of a 500 kb region on 17q25 and the exclusion of candidate genes as the familial Tylosis Oesophageal Cancer (TOC) locus
Janet M Risk, Kathryn E Evans, Joanne Jones, et al.
Journal of the American Academy of Dermatology
|
March 8, 2022
Risk factors for metastatic cutaneous squamous cell carcinoma: Refinement and replication based on 2 nationwide nested case-control studies
Selin Tokez, Zoe C Venables, Loes M Hollestein, et al.
Human Molecular Genetics
|
May 20, 1999
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma
L Rickman, D Simrak, H P Stevens, et al.
Page
of 53
Search research articles
Search
Showing results (431-440 of 525) with videos related to
Sort By:
Page
of 53
Nature Communications
|
January 28, 2017
Rhomboid family member 2 regulates cytoskeletal stress-associated Keratin 16
Thiviyani Maruthappu, Anissa Chikh, Benjamin Fell, et al.
Human Mutation
|
June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia
M Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
Cancer Genetics and Cytogenetics
|
November 19, 2003
Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability
N A Alam, P Gorman, E E M Jaeger, et al.
Journal of Cell Science
|
July 4, 2003
Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability
Andrew P South, Hong Wan, Michael G Stone, et al.
Journal of the National Cancer Institute
|
June 19, 1996
Human papillomavirus infections in nonmelanoma skin cancers from renal transplant recipients and nonimmunosuppressed patients
V Shamanin, H zur Hausen, D Lavergne, et al.
NPJ Precision Oncology
|
September 2, 2025
Enhanced metastasis risk prediction in cutaneous squamous cell carcinoma using deep learning and computational histopathology
Emilia Peleva, Yue Chen, Bernhard Finke, et al.
The British Journal of Dermatology
|
March 14, 2019
Epidemiology of basal and cutaneous squamous cell carcinoma in the U.K. 2013-15: a cohort study
Z C Venables, T Nijsten, K F Wong, et al.
Oncogene
|
September 6, 2002
Characterization of a 500 kb region on 17q25 and the exclusion of candidate genes as the familial Tylosis Oesophageal Cancer (TOC) locus
Janet M Risk, Kathryn E Evans, Joanne Jones, et al.
Journal of the American Academy of Dermatology
|
March 8, 2022
Risk factors for metastatic cutaneous squamous cell carcinoma: Refinement and replication based on 2 nationwide nested case-control studies
Selin Tokez, Zoe C Venables, Loes M Hollestein, et al.
Human Molecular Genetics
|
May 20, 1999
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma
L Rickman, D Simrak, H P Stevens, et al.
Page
of 53