Search research articles
Contact Us
Filters
Showing results (511-520 of 649) with videos related to
Page
of 65
Sort By:
Nature Genetics
|
December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevus
E L Rugg, W H McLean, W E Allison, et al.
The British Journal of Dermatology
|
August 8, 2009
Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation
J K Gass, N J Wilson, F J D Smith, et al.
The Journal of Investigative Dermatology
|
September 1, 1994
Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene
H Kremer, P Zeeuwen, W H McLean, et al.
Nature Genetics
|
September 6, 2000
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension
, K B Lane, R D Machado, et al.
Neurology. Clinical Practice
|
November 13, 2025
How Patients With Amyotrophic Lateral Sclerosis Perceive Respiratory Interventions: A Mixed-Methods Study to Inform Implementation Efforts
Jason Ackrivo, Danny Bracy, Lauren B Elman, et al.
Plos Genetics
|
October 8, 2013
Direct monitoring of the strand passage reaction of DNA topoisomerase II triggers checkpoint activation
Katherine L Furniss, Hung-Ji Tsai, Jo Ann W Byl, et al.
Pediatric Neurology
|
March 29, 2017
Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors
John T Killian, Jane B Lane, Hye-Seung Lee, et al.
Implementation Science Communications
|
November 7, 2023
Evaluation of a brief virtual implementation science training program: the Penn Implementation Science Institute
Amelia E Van Pelt, Christopher P Bonafide, Katharine A Rendle, et al.
Archives of Dermatological Research
|
January 1, 1990
An investigation of cytokeratin expression in skin epithelial cysts and some uncommon types of cystic tumours using chain-specific antibodies
D Broekaert, L Goeman, F C Ramaekers, et al.
Nature Genetics
|
November 5, 1997
Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome
J A McGrath, J R McMillan, C S Shemanko, et al.
Page
of 65
Search research articles
Search
Showing results (511-520 of 649) with videos related to
Sort By:
Page
of 65
Nature Genetics
|
December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevus
E L Rugg, W H McLean, W E Allison, et al.
The British Journal of Dermatology
|
August 8, 2009
Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation
J K Gass, N J Wilson, F J D Smith, et al.
The Journal of Investigative Dermatology
|
September 1, 1994
Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene
H Kremer, P Zeeuwen, W H McLean, et al.
Nature Genetics
|
September 6, 2000
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension
, K B Lane, R D Machado, et al.
Neurology. Clinical Practice
|
November 13, 2025
How Patients With Amyotrophic Lateral Sclerosis Perceive Respiratory Interventions: A Mixed-Methods Study to Inform Implementation Efforts
Jason Ackrivo, Danny Bracy, Lauren B Elman, et al.
Plos Genetics
|
October 8, 2013
Direct monitoring of the strand passage reaction of DNA topoisomerase II triggers checkpoint activation
Katherine L Furniss, Hung-Ji Tsai, Jo Ann W Byl, et al.
Pediatric Neurology
|
March 29, 2017
Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors
John T Killian, Jane B Lane, Hye-Seung Lee, et al.
Implementation Science Communications
|
November 7, 2023
Evaluation of a brief virtual implementation science training program: the Penn Implementation Science Institute
Amelia E Van Pelt, Christopher P Bonafide, Katharine A Rendle, et al.
Archives of Dermatological Research
|
January 1, 1990
An investigation of cytokeratin expression in skin epithelial cysts and some uncommon types of cystic tumours using chain-specific antibodies
D Broekaert, L Goeman, F C Ramaekers, et al.
Nature Genetics
|
November 5, 1997
Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome
J A McGrath, J R McMillan, C S Shemanko, et al.
Page
of 65