| Tissue-expressed B7x affects the immune response to and outcome of lethal pulmonary infection. Hofmeyer K.A., Scandiuzzi L., Ghosh K., Pirofski L.A., Zang X.
J. Immunol. 189:3054-3063(2012) · Mapped (6) |
| Structural and biochemical characterization of human adenylosuccinate lyase (ADSL) and the R303C ADSL deficiency-associated mutation. Ray S.P., Deaton M.K., Capodagli G.C., Calkins L.A., Sawle L., Ghosh K., Patterson D., Pegan S.D.
Biochemistry 51:6701-6713(2012) · UniProtKB (1) · Mapped (6) |
| FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India. Ghosh K., Swaminathan S., Madkaikar M., Gupta M., Kerketta L., Vundinti B.
Ann. Hematol. 91:1703-1712(2012) · Mapped (6) |
| Hereditary protein C deficiency in Indian patients with venous thrombosis. Pai N., Ghosh K., Shetty S.
Ann. Hematol. 91:1471-1476(2012) · Mapped (20) |
| Fc gamma R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients. Pradhan V., Patwardhan M., Nadkarni A., Ghosh K.
Indian J. Med. Res. 134:181-185(2011) · Mapped (6) |
| CCR5 chemokine receptor polymorphism in patients with HIV-1 from Western India. Shankarkumar A., Shankarkumar U., Ghosh K.
J. Acquir. Immune Defic. Syndr. 57:e21-e21(2011) · Mapped (22) |
| Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected. Shanbhag S., Shetty S., Ghosh K.
Haemophilia 17:e843-5(2011) · Mapped (4) |
| Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein. Basu A., Jain P., Sarkar P., Gangodkar S., Deshpande D., Ganti K., Shetty S., Ghosh K.
FEMS Immunol. Med. Microbiol. 62:140-147(2011) · Mapped (3) |
| Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutations. Kedar P.S., Warang P., Ghosh K., Colah R.B.
Am. J. Hematol. 86:327-329(2011) · Mapped (5) |
| Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adults. D'Silva S., Borse V., Colah R.B., Ghosh K., Mukherjee M.B.
Genet Test Mol Biomarkers 15:215-218(2011) · Mapped (6) |
| Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations. Nair P.S., Shetty S., Kulkarni B., Ghosh K.
Clin. Chim. Acta 411:2004-2008(2010) · Mapped (12) |
| Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D. Shmukler B.E., Kedar P.S., Warang P., Desai M., Madkaikar M., Ghosh K., Colah R.B., Alper S.L.
Am. J. Hematol. 85:824-828(2010) · Mapped (9) |
| PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility. Pradhan V., Borse V., Ghosh K.
J Postgrad Med 56:239-242(2010) · Mapped (6) |
| The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies. Italia K.Y., Jijina F.F., Jain D., Merchant R., Nadkarni A.H., Mukherjee M., Ghosh K., Colah R.B.
Clin. Biochem. 43:1329-1332(2010) · Mapped (15) |
| Increase in surface hydrophobicity of the cataract-associated P23T mutant of human gammaD-crystallin is responsible for its dramatically lower, retrograde solubility. Pande A., Ghosh K.S., Banerjee P.R., Pande J.
Biochemistry 49:6122-6129(2010) · Mapped (1) |
| JAK2 mutations across a spectrum of venous thrombosis cases. Shetty S., Kulkarni B., Pai N., Mukundan P., Kasatkar P., Ghosh K.
Am. J. Clin. Pathol. 134:82-85(2010) · Mapped (6) |
| Fc gamma R IIIB polymorphisms: their association with clinical manifestations and autoantibodies in SLE patients from western India. Pradhan V., Deshpande N., Nadkarni A., Patwardhan M., Surve P., Ghosh K.
Int J Rheum Dis 13:138-143(2010) · Mapped (2) |
| Restriction fragment length polymorphism (RFLP) of the X chromosome linked glucose-6-phosphate dehydrogenase (G6PD) locus in India. Chalvam R., Colah R.B., Mohanty D., Ghosh K., Mukherjee M.B.
Ann. Hum. Biol. 38:106-109(2011) · Mapped (7) |
| Aromatase immunoreactivity is increased in mammographically dense regions of the breast. Vachon C.M., Sasano H., Ghosh K., Brandt K.R., Watson D.A., Reynolds C., Lingle W.L., Goss P.E., Li R., Aiyar S.E. et al.
Breast Cancer Res. Treat. 125:243-252(2011) · Mapped (9) |
| Requirements for catalysis in the Cre recombinase active site. Gibb B., Gupta K., Ghosh K., Sharp R., Chen J., Van Duyne G.D.
Nucleic Acids Res. 38:5817-5832(2010) · Mapped (1) |
| Association of factor VII gene polymorphisms with Budd Chiari syndrome. Jain A., Shetty S., Kulkarni B., Ghosh K.
Blood Coagul. Fibrinolysis 21:296-297(2010) · Mapped (5) |
| Human leucocyte antigen class II DRB1 and DQB1 associations in human immunodeficiency virus-infected patients of Mumbai, India. Shankarkumar U., Pawar A., Ghosh K., Bajpai S., Pazare A.
Int. J. Immunogenet. 37:199-204(2010) · Mapped (486) |
| Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. Colah R., Gorakshakar A., Phanasgaonkar S., D'Souza E., Nadkarni A., Surve R., Sawant P., Master D., Patel R., Ghosh K. et al.
Br. J. Haematol. 149:739-747(2010) · Mapped (38) |
| Association of HLA alleles with hepatitis C infection in Maharashtra, western India. Tripathy A.S., Shankarkumar U., Chadha M.S., Ghosh K., Arankalle V.A.
Indian J. Med. Res. 130:550-555(2009) · Mapped (1,894) |
| Protein C (PROC) gene mutations in two Indian families with purpura fulminans. Pai N., Shetty S., Ghosh K.
Ann. Hematol. 89:835-836(2010) · Mapped (20) |
