Search Results - "Jain, Hemani"

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    Role of Cytogenetics and Fluorescence In Situ Hybridization in the Laboratory Workup of Acute Myeloid Leukemias by Jain, Hemani, Shetty, Dhanlaxmi

    “…Abstract A new understanding of acute myeloid leukemia as a varied group of unique biologic entity has emerged, as a result of the identification of various…”
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    Journal Article
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    Emergence of an unrelated highly aberrant clone in an AML patient at relapse four months after peripheral blood stem cell transplantation by Kadam, Pratibha S, Jain, Hemani V, Parikh, Purvish M, Saikia, Tapan K, Agarwal, Sandhya, Ambulkar, Indu

    Published in Indian journal of human genetics (01-09-2007)
    “…We report a case of AML-M1 with 5q aberration at diagnosis. The patient was treated with high-dose chemotherapy (HDCT). After remission induction, he received…”
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    Journal Article
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    Evaluation of cytogenetic response in CML patients with variant Philadelphia translocation by Shetty, Dhanlaxmi, Talker, Elizabeth, Jain, Hemani, Talker, Judith, Patkar, Nikhil, Subramanian, Papagudi, Jain, Hasmukh, Bonda, Avinash, Punatar, Sachin, Gokarn, Anant, Bagal, Bhausaheb, Sengar, Manju, Khattry, Navin

    Published in Asia-Pacific journal of clinical oncology (01-02-2022)
    “…Background and aim Molecular mechanism of translocation and outcome in variant chronic myeloid leukaemia (vCML) has been a topic of debate. While several…”
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    Journal Article
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    A novel case of intrachromosomal amplification and insertion of RUNX1 on derivative chromosome 2 in pediatric AML by Jain, Hemani, Shetty, Dhanlaxmi, Roy Moulik, Nirmalya, Narula, Gaurav, Subramanian, P.G., Banavali, Sripad

    Published in Cancer genetics (01-06-2021)
    “…Intrachromosomal amplification of RUNX1 gene on chromosome 21 (iAMP21) is a rare occurrence in acute myeloid leukemia (AML). Herein, we describe a case of AML…”
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    A rare case of hepatosplenic γδ T-cell lymphoma expressing CD19 with ring chromosome 7 and trisomy 8 by Jain, Hemani, Shetty, Dhanlaxmi, Jain, Hasmukh, Sengar, Manju, Khattry, Navin, Subramanian, P.G.

    Published in Cancer genetics (01-12-2018)
    “…•Presenting CD19 positive HSTL with amplification of 7q forming ring chromosome 7 and trisomy 8.•This is a new finding in γδ HSTL and not yet reported in the…”
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    Journal Article
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    Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia by Pais, Anurita, Amare Kadam, Pratibha, Raje, Gauri, Sawant, Manisha, Kabre, Sharayu, Jain, Hemani, Advani, Suresh, Banavali, Shripad

    Published in Leukemia research (01-05-2005)
    “…Studies were done to investigate MLL gene aberrations using Conventional Cytogenetics, Southern blotting as well as FISH using a panel of probes on 218 cases…”
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    Emergence of an unrelated highly aberrant clone in an AML patient at relapse four months after peripheral blood stem cell transplantation by Kadam, Pratibha S. Amare, Jain, Hemani V, Parikh, Purvish M, Saikia, Tapan K, Agarwal, Sandhya, Ambulkar, Indu

    Published in Indian journal of human genetics (06-02-2008)
    “…We report a case of AML-M1 with 5q aberration at diagnosis. The patient was treated with high-dose chemotherapy (HDCT). After remission induction, he received…”
    Get full text
    Journal Article
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    A rare case of hepatosplenic γδ T-cell lymphoma expressing CD19 with ring chromosome 7 and trisomy 8 by Jain, Hemani, Shetty, Dhanlaxmi, Jain, Hasmukh, Sengar, Manju, Khattry, Navin, Subramanian, P G

    Published in Cancer genetics (01-12-2018)
    “…Hepatosplenic T-cell lymphoma (HSTL) is a rare subtype of peripheral T-cell lymphoma predominantly seen in young males. This disease presents with isolated…”
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