Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Peter N Robinson

Showing results (71-80 of 348) with videos related to

Pageof 35
Sort By:
The International Journal of Biochemistry & Cell Biology|December 25, 2012
miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling moleculesRaghu Bhushan, Johannes Grünhagen, Jessica Becker, et al.
Molecular Vision|December 15, 2007
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian originVanita Vanita, Jai Rup Singh, Daljit Singh, et al.
Future Healthcare Journal|August 1, 2019
Care homes learning together initiative: a collaborative approach to care home medicinePeter N Robinson, Anna Steel, Helen Hopwood, et al.
Nucleic Acids Research|December 8, 2016
L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomesTobias Penzkofer, Marten Jäger, Marek Figlerowicz, et al.
Bioinformatics (Oxford, England)|July 9, 2021
HEMDAG: a family of modular and scalable hierarchical ensemble methods to improve Gene Ontology term predictionMarco Notaro, Marco Frasca, Alessandro Petrini, et al.
European Journal of Medical Genetics|June 23, 2015
FGFR2 mutation in a patient without typical features of Pfeiffer syndrome--The emerging role of combined NGS and phenotype based strategiesRicarda Flöttmann, Alexej Knaus, Tomasz Zemojtel, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Further evidence for FGF16 truncating mutations as the cause of X-linked recessive fusion of metacarpals 4 / 5Aleksander Jamsheer, Robert Smigiel, Aleksandra Jakubiak, et al.
BMC Medical Informatics and Decision Making|August 2, 2012
Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of Cerebrotendinous xanthomatosisMaría Taboada, Diego Martínez, Belén Pilo, et al.
Bioinformatics (Oxford, England)|May 20, 2015
IMSEQ--a fast and error aware approach to immunogenetic sequence analysisLeon Kuchenbecker, Mikalai Nienen, Jochen Hecht, et al.
Cytogenetic and Genome Research|March 5, 2026
Familial Robertsonian Translocation, rob(14;21), with high risk for Down syndromeAnna Rajab, Heidemarie Neitzel, Jenny Jalali, et al.
Pageof 35

Showing results (71-80 of 348) with videos related to

Sort By:
Pageof 35
The International Journal of Biochemistry & Cell Biology|December 25, 2012
miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling moleculesRaghu Bhushan, Johannes Grünhagen, Jessica Becker, et al.
Molecular Vision|December 15, 2007
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian originVanita Vanita, Jai Rup Singh, Daljit Singh, et al.
Future Healthcare Journal|August 1, 2019
Care homes learning together initiative: a collaborative approach to care home medicinePeter N Robinson, Anna Steel, Helen Hopwood, et al.
Nucleic Acids Research|December 8, 2016
L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomesTobias Penzkofer, Marten Jäger, Marek Figlerowicz, et al.
Bioinformatics (Oxford, England)|July 9, 2021
HEMDAG: a family of modular and scalable hierarchical ensemble methods to improve Gene Ontology term predictionMarco Notaro, Marco Frasca, Alessandro Petrini, et al.
European Journal of Medical Genetics|June 23, 2015
FGFR2 mutation in a patient without typical features of Pfeiffer syndrome--The emerging role of combined NGS and phenotype based strategiesRicarda Flöttmann, Alexej Knaus, Tomasz Zemojtel, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Further evidence for FGF16 truncating mutations as the cause of X-linked recessive fusion of metacarpals 4 / 5Aleksander Jamsheer, Robert Smigiel, Aleksandra Jakubiak, et al.
BMC Medical Informatics and Decision Making|August 2, 2012
Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of Cerebrotendinous xanthomatosisMaría Taboada, Diego Martínez, Belén Pilo, et al.
Bioinformatics (Oxford, England)|May 20, 2015
IMSEQ--a fast and error aware approach to immunogenetic sequence analysisLeon Kuchenbecker, Mikalai Nienen, Jochen Hecht, et al.
Cytogenetic and Genome Research|March 5, 2026
Familial Robertsonian Translocation, rob(14;21), with high risk for Down syndromeAnna Rajab, Heidemarie Neitzel, Jenny Jalali, et al.
Pageof 35