المؤلفون: Devroop Sarkar, Kunal Ray, Mainak Sengupta

المصدر: BioMed Research International, Vol 2014 (2014)

مصطلحات موضوعية: Medicine

Relation: http://dx.doi.org/10.1155/2014/673895; https://doaj.org/toc/2314-6133; https://doaj.org/toc/2314-6141; https://doaj.org/article/21587b9221cd494db1f9d66bf5092ce3

الاتاحة: https://doi.org/10.1155/2014/673895
https://doaj.org/article/21587b9221cd494db1f9d66bf5092ce3

المؤلفون: Kausik Ganguly, Devroop Sarkar, Asim Sil, Kunal Ray, Mainak Sengupta, Arpan Saha, Tithi Dutta

المصدر: Annals of human geneticsREFERENCES. 84(3)

مصطلحات موضوعية: Tyr gene, DNA Mutational Analysis, Ethnic group, India, Biology, 03 medical and health sciences, Genetics, medicine, Ethnicity, Humans, Gene, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Monophenol Monooxygenase, 030305 genetics & heredity, Haplotype, medicine.disease, Oculocutaneous albinism, Founder Effect, Pedigree, Haplotypes, Albinism, Oculocutaneous, Albinism, West bengal, Founder effect

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd94c5494272e9bf7fb6bdb9dd3f1473
https://pubmed.ncbi.nlm.nih.gov/32115698

المؤلفون: S. Bhaskar, Kausik Ganguly, Debmalya Sengupta, Devroop Sarkar, Mainak Sengupta, Kunal Ray

المصدر: Haemophilia : the official journal of the World Federation of Hemophilia. 21(5)

مصطلحات موضوعية: medicine.medical_specialty, In silico, Haemophilia A, Static Electricity, Mutation, Missense, Biology, Hemophilia A, hemic and lymphatic diseases, Molecular genetics, medicine, Missense mutation, Humans, Computer Simulation, Genetic Predisposition to Disease, Genetics (clinical), Conserved Sequence, Genetics, Factor VIII, Genetic heterogeneity, Protein Stability, Hydrogen Bonding, Hematology, General Medicine, medicine.disease, Phenotype, Protein Structure, Tertiary, Amino Acid Substitution, Mutation testing, Solvents, Software

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62a9a9975e590ebafede4c66333bd5b6
https://pubmed.ncbi.nlm.nih.gov/25952765

المؤلفون: Devroop, Sarkar

المصدر: The National medical journal of India. 26(4)

مصطلحات موضوعية: Biomedical Research, Career Choice, Educational Status, Humans, India

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::2a6cbb1a8bc8b87fc0a0159503cfc1d7
https://pubmed.ncbi.nlm.nih.gov/24758466

المؤلفون: Devroop Sarkar, Asim Sil, Mainak Sengupta, Maitreyee Mondal, Swapan Samanta, Kunal Ray

المصدر: Journal of genetics. 92(2)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Skin Neoplasms, Adolescent, DNA Mutational Analysis, India, Biology, Melanin, Young Adult, Risk Factors, Genetics, medicine, Humans, Basal cell carcinoma, Genetic Predisposition to Disease, Young adult, Melanoma, Case-control study, Middle Aged, medicine.disease, Dermatology, Oculocutaneous albinism, Albinism, Oculocutaneous, Case-Control Studies, Albinism, Female, Skin cancer, Receptor, Melanocortin, Type 1

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49cae15b4d9540f9b7e3552a4ddf2a6b
https://pubmed.ncbi.nlm.nih.gov/23970088

المؤلفون: Devroop Sarkar, Kunal Ray, Mainak Sengupta

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://downloads.hindawi.com/journals/bmri/2014/673895.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1077.2718; http://downloads.hindawi.com/journals/bmri/2014/673895.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1077.2718
http://downloads.hindawi.com/journals/bmri/2014/673895.pdf

المؤلفون: Mainak Sengupta, Devroop Sarkar, Maitreyee Mondal, Swapan Samanta, Asim Sil

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.ias.ac.in/jgenet/Vol92No2/305.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.667.974; http://www.ias.ac.in/jgenet/Vol92No2/305.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.667.974
http://www.ias.ac.in/jgenet/Vol92No2/305.pdf