P Lunt - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

P Lunt

Showing results (21-30 of 24) with videos related to

Pageof 3

Sort By:

You have reached the last page of results.This site can display upto 24 results.

Neurology|June 1, 2012

A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1D L Raja Rayan, A Haworth, R Sud, et al.

Human Mutation|January 1, 1997

Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.

Science (New York, N.Y.)|August 2, 2008

Hopping hotspots: global shifts in marine biodiversityW Renema, D R Bellwood, J C Braga, et al.

Nature Communications|January 14, 2026

Dynamic allele usage of X-linked genes ameliorates neurodevelopmental disease phenotypes in brain organoidsM Bertin, H Todorov, S Frank, et al.

Pageof 3

Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

Neurology|June 1, 2012

A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1D L Raja Rayan, A Haworth, R Sud, et al.

Human Mutation|January 1, 1997

Nine novel L1 CAM mutations in families with X-linked hydrocephalusJ R MacFarlane, J S Du, M E Pepys, et al.

Science (New York, N.Y.)|August 2, 2008

Hopping hotspots: global shifts in marine biodiversityW Renema, D R Bellwood, J C Braga, et al.

Nature Communications|January 14, 2026

Dynamic allele usage of X-linked genes ameliorates neurodevelopmental disease phenotypes in brain organoidsM Bertin, H Todorov, S Frank, et al.

Pageof 3