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B Lane

Showing results (511-520 of 649) with videos related to

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Nature Genetics|December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevusE 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 mutationJ 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 geneH 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 EffortsJason 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 activationKatherine L Furniss, Hung-Ji Tsai, Jo Ann W Byl, et al.
Pediatric Neurology|March 29, 2017
Scoliosis in Rett Syndrome: Progression, Comorbidities, and PredictorsJohn 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 InstituteAmelia 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 antibodiesD 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 syndromeJ A McGrath, J R McMillan, C S Shemanko, et al.
Pageof 65

Showing results (511-520 of 649) with videos related to

Sort By:
Pageof 65
Nature Genetics|December 1, 1995
A mutation in the mucosal keratin K4 is associated with oral white sponge nevusE 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 mutationJ 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 geneH 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 EffortsJason 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 activationKatherine L Furniss, Hung-Ji Tsai, Jo Ann W Byl, et al.
Pediatric Neurology|March 29, 2017
Scoliosis in Rett Syndrome: Progression, Comorbidities, and PredictorsJohn 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 InstituteAmelia 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 antibodiesD 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 syndromeJ A McGrath, J R McMillan, C S Shemanko, et al.
Pageof 65