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Nilanjan Sengupta

Showing results (11-20 of 55) with videos related to

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Cureus|March 28, 2022
A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase DeficiencyDeep Hathi, Soumik Goswami, Nilanjan Sengupta, et al.
Indian Journal of Endocrinology and Metabolism|October 27, 2011
Human immunodeficiency virus endocrinopathyUma Sinha, Nilanjan Sengupta, Prasanta Mukhopadhyay, et al.
Indian Journal of Endocrinology and Metabolism|June 19, 2013
Recurrent hypokalemic paralysis: An atypical presentation of hypothyroidismUma Sinha, Nilanjan Sengupta, Keshab Sinharay, et al.
Indian Journal of Endocrinology and Metabolism|May 26, 2012
Acromegaly without acral changes: A rare presentationNilanjan Sengupta, Uma Sinha, Keshab Sinha Roy, et al.
Indian Journal of Endocrinology and Metabolism|December 11, 2012
Rare presentation of a common disease: Idiopathic hypoparathyroidism presenting with extrapyramidal symptoms and status epilepticusKaushik Ghosh, Nilanjan Sengupta, Tanmoy Jyoti Sau, et al.
Gene|November 18, 2005
Acetylation and deacetylation of non-histone proteinsMichele A Glozak, Nilanjan Sengupta, Xiaohong Zhang, et al.
Indian Journal of Dermatology|August 20, 2015
A Florid Case of Iatrogenic Cushing's Syndrome Induced by Topical Steroid with Osteoporosis and HypogonadismPranab Kumar Sahana, Nilendu Sarma, Nilanjan Sengupta, et al.
Cureus|March 21, 2022
Absence of Vitamin D Deficiency Among Outdoor Workers With Type 2 Diabetes Mellitus in Southern West Bengal, IndiaSoumik Goswami, Neha Agrawal, Nilanjan Sengupta, et al.
Molecular and Cellular Biology|July 1, 2006
Histone deacetylase 8 safeguards the human ever-shorter telomeres 1B (hEST1B) protein from ubiquitin-mediated degradationHeehyoung Lee, Nilanjan Sengupta, Alejandro Villagra, et al.
Indian Journal of Endocrinology and Metabolism|November 20, 2013
An unusual case of episodic quadriparesisMukut Roy, Pranab Kumar Sahana, Nilanjan Sengupta, et al.
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
Cureus|March 28, 2022
A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase DeficiencyDeep Hathi, Soumik Goswami, Nilanjan Sengupta, et al.
Indian Journal of Endocrinology and Metabolism|October 27, 2011
Human immunodeficiency virus endocrinopathyUma Sinha, Nilanjan Sengupta, Prasanta Mukhopadhyay, et al.
Indian Journal of Endocrinology and Metabolism|June 19, 2013
Recurrent hypokalemic paralysis: An atypical presentation of hypothyroidismUma Sinha, Nilanjan Sengupta, Keshab Sinharay, et al.
Indian Journal of Endocrinology and Metabolism|May 26, 2012
Acromegaly without acral changes: A rare presentationNilanjan Sengupta, Uma Sinha, Keshab Sinha Roy, et al.
Indian Journal of Endocrinology and Metabolism|December 11, 2012
Rare presentation of a common disease: Idiopathic hypoparathyroidism presenting with extrapyramidal symptoms and status epilepticusKaushik Ghosh, Nilanjan Sengupta, Tanmoy Jyoti Sau, et al.
Gene|November 18, 2005
Acetylation and deacetylation of non-histone proteinsMichele A Glozak, Nilanjan Sengupta, Xiaohong Zhang, et al.
Indian Journal of Dermatology|August 20, 2015
A Florid Case of Iatrogenic Cushing's Syndrome Induced by Topical Steroid with Osteoporosis and HypogonadismPranab Kumar Sahana, Nilendu Sarma, Nilanjan Sengupta, et al.
Cureus|March 21, 2022
Absence of Vitamin D Deficiency Among Outdoor Workers With Type 2 Diabetes Mellitus in Southern West Bengal, IndiaSoumik Goswami, Neha Agrawal, Nilanjan Sengupta, et al.
Molecular and Cellular Biology|July 1, 2006
Histone deacetylase 8 safeguards the human ever-shorter telomeres 1B (hEST1B) protein from ubiquitin-mediated degradationHeehyoung Lee, Nilanjan Sengupta, Alejandro Villagra, et al.
Indian Journal of Endocrinology and Metabolism|November 20, 2013
An unusual case of episodic quadriparesisMukut Roy, Pranab Kumar Sahana, Nilanjan Sengupta, et al.
Pageof 6