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Waheeda A Hossain

Showing results (1-10 of 24) with videos related to

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Frontiers in Genetics|June 8, 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databasesWaheeda A Hossain, Merlin G Butler
Journal of Neuroscience Research|April 29, 2008
Interactive roles of fibroblast growth factor 2 and neurotrophin 3 in the sequence of migration, process outgrowth, and axonal differentiation of mouse cochlear ganglion cellsWaheeda A Hossain, Chrystal D'Sa, D Kent Morest
Journal of Neurobiology|May 5, 2006
Site-specific interactions of neurotrophin-3 and fibroblast growth factor (FGF2) in the embryonic development of the mouse cochlear nucleusWaheeda A Hossain, Chrystal D'Sa, D Kent Morest
Journal of Neuroscience Research|February 14, 2003
Intracellular fibroblast growth factor produces effects different from those of extracellular application on development of avian cochleovestibular ganglion cells in vitroMasako M Bilak, Waheeda A Hossain, D Kent Morest
International Journal of Molecular Sciences|January 21, 2023
Chromosomal Microarray Study in Prader-Willi SyndromeMerlin G Butler, Waheeda A Hossain, Neil Cowen, et al.
BMC Medical Genomics|August 2, 2022
Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional studyOlivia J Veatch, Jacob Steinle, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Preliminary observations of mitochondrial dysfunction in Prader-Willi syndromeMerlin G Butler, Waheeda A Hossain, Robert Tessman, et al.
Hearing Research|August 19, 2005
Biotinidase reveals the morphogenetic sequence in cochlea and cochlear nucleus of miceCraig L Brumwell, Waheeda A Hossain, D Kent Morest, et al.
American Journal of Medical Genetics. Part A|February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and reviewSamantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disordersJacob Steinle, Waheeda A Hossain, Scott Lovell, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Frontiers in Genetics|June 8, 2026
Identification and molecular functional analysis of genes associated with addiction using integrated genetic web-based programs and databasesWaheeda A Hossain, Merlin G Butler
Journal of Neuroscience Research|April 29, 2008
Interactive roles of fibroblast growth factor 2 and neurotrophin 3 in the sequence of migration, process outgrowth, and axonal differentiation of mouse cochlear ganglion cellsWaheeda A Hossain, Chrystal D'Sa, D Kent Morest
Journal of Neurobiology|May 5, 2006
Site-specific interactions of neurotrophin-3 and fibroblast growth factor (FGF2) in the embryonic development of the mouse cochlear nucleusWaheeda A Hossain, Chrystal D'Sa, D Kent Morest
Journal of Neuroscience Research|February 14, 2003
Intracellular fibroblast growth factor produces effects different from those of extracellular application on development of avian cochleovestibular ganglion cells in vitroMasako M Bilak, Waheeda A Hossain, D Kent Morest
International Journal of Molecular Sciences|January 21, 2023
Chromosomal Microarray Study in Prader-Willi SyndromeMerlin G Butler, Waheeda A Hossain, Neil Cowen, et al.
BMC Medical Genomics|August 2, 2022
Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional studyOlivia J Veatch, Jacob Steinle, Waheeda A Hossain, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Preliminary observations of mitochondrial dysfunction in Prader-Willi syndromeMerlin G Butler, Waheeda A Hossain, Robert Tessman, et al.
Hearing Research|August 19, 2005
Biotinidase reveals the morphogenetic sequence in cochlea and cochlear nucleus of miceCraig L Brumwell, Waheeda A Hossain, D Kent Morest, et al.
American Journal of Medical Genetics. Part A|February 14, 2018
Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and reviewSamantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disordersJacob Steinle, Waheeda A Hossain, Scott Lovell, et al.
Pageof 3