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B Mukherjee

Showing results (451-460 of 524) with videos related to

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Molecular Genetics and Metabolism|September 20, 2000
Human acid ceramidase gene: novel mutations in Farber diseaseZ Zhang, A K Mandal, A Mital, et al.
Indian Journal of Human Genetics|November 20, 2010
Microsatellite diversity among the primitive tribes of IndiaMalay B Mukherjee, V Tripathy, R B Colah, et al.
Human Molecular Genetics|July 11, 2015
Cln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disordersGoutam Chandra, Maria B Bagh, Shiyong Peng, et al.
Oncogene|August 1, 1994
Allelic loss and somatic differentiation in human male germ cell tumorsV V Murty, G J Bosl, J Houldsworth, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|August 22, 2018
First Observation of Hb Lepore Hollandia in the Baiga Tribal FamilyHarsha Lad, Manju Yadav, Pallavi Mehta, et al.
International Archives of Allergy and Applied Immunology|January 1, 1988
Relationship between leukotriene C4 and an uteroglobin-like protein in nasal and tracheobronchial mucosa of children. Implication in acute respiratory illnessesB Volovitz, I Nathanson, G DeCastro, et al.
Nature Communications|March 8, 2017
Misrouting of v-ATPase subunit V0a1 dysregulates lysosomal acidification in a neurodegenerative lysosomal storage disease modelMaria B Bagh, Shiyong Peng, Goutam Chandra, et al.
Gene|May 8, 1999
Palmitoyl-protein thioesterase gene expression in the developing mouse brain and retina: implications for early loss of vision in infantile neuronal ceroid lipofuscinosisZ Zhang, A K Mandal, N Wang, et al.
Journal of Inherited Metabolic Disease|April 13, 2020
Cln1-mutations suppress Rab7-RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosisChinmoy Sarkar, Tamal Sadhukhan, Maria B Bagh, et al.
British Journal of Haematology|July 6, 2018
Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell diseasePrashant Warang, Takujiro Homma, Riddhi Pandya, et al.
Pageof 53

Showing results (451-460 of 524) with videos related to

Sort By:
Pageof 53
Molecular Genetics and Metabolism|September 20, 2000
Human acid ceramidase gene: novel mutations in Farber diseaseZ Zhang, A K Mandal, A Mital, et al.
Indian Journal of Human Genetics|November 20, 2010
Microsatellite diversity among the primitive tribes of IndiaMalay B Mukherjee, V Tripathy, R B Colah, et al.
Human Molecular Genetics|July 11, 2015
Cln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disordersGoutam Chandra, Maria B Bagh, Shiyong Peng, et al.
Oncogene|August 1, 1994
Allelic loss and somatic differentiation in human male germ cell tumorsV V Murty, G J Bosl, J Houldsworth, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|August 22, 2018
First Observation of Hb Lepore Hollandia in the Baiga Tribal FamilyHarsha Lad, Manju Yadav, Pallavi Mehta, et al.
International Archives of Allergy and Applied Immunology|January 1, 1988
Relationship between leukotriene C4 and an uteroglobin-like protein in nasal and tracheobronchial mucosa of children. Implication in acute respiratory illnessesB Volovitz, I Nathanson, G DeCastro, et al.
Nature Communications|March 8, 2017
Misrouting of v-ATPase subunit V0a1 dysregulates lysosomal acidification in a neurodegenerative lysosomal storage disease modelMaria B Bagh, Shiyong Peng, Goutam Chandra, et al.
Gene|May 8, 1999
Palmitoyl-protein thioesterase gene expression in the developing mouse brain and retina: implications for early loss of vision in infantile neuronal ceroid lipofuscinosisZ Zhang, A K Mandal, N Wang, et al.
Journal of Inherited Metabolic Disease|April 13, 2020
Cln1-mutations suppress Rab7-RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosisChinmoy Sarkar, Tamal Sadhukhan, Maria B Bagh, et al.
British Journal of Haematology|July 6, 2018
Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell diseasePrashant Warang, Takujiro Homma, Riddhi Pandya, et al.
Pageof 53