Publications by authors named "Bidisha Saha"

17Publications

Potassium acts through mTOR to regulate its own secretion.

Authors:
Mads Vaarby Sørensen Bidisha Saha Iben Skov Jensen Peng Wu Niklas Ayasse Catherine E Gleason Samuel Levi Svendsen Wen-Hui Wang David Pearce

JCI Insight 2019 04 23;5. Epub 2019 Apr 23.

Department of Medicine, Division of Nephrology, and Department of Cellular and Molecular Pharmacology, UCSF, San Francisco, California, USA.

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April 2019

Phosphorylation at distinct subcellular locations underlies specificity in mTORC2-mediated activation of SGK1 and Akt.

Authors:
Catherine E Gleason Juan A Oses-Prieto Kathy H Li Bidisha Saha Gavin Situ Alma L Burlingame David Pearce

J Cell Sci 2019 04 9;132(7). Epub 2019 Apr 9.

Department of Medicine, Division of Nephrology, UCSF, San Francisco, CA 94143, USA.

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April 2019

Dysfunction of the MDM2/p53 axis is linked to premature aging.

Authors:
Davor Lessel Danyi Wu Carlos Trujillo Thomas Ramezani Ivana Lessel Mohammad K Alwasiyah Bidisha Saha Fuki M Hisama Katrin Rading Ingrid Goebel Petra Schütz Günter Speit Josef Högel Holger Thiele Gudrun Nürnberg Peter Nürnberg Matthias Hammerschmidt Yan Zhu David R Tong Chen Katz George M Martin Junko Oshima Carol Prives Christian Kubisch

J Clin Invest 2017 Oct 28;127(10):3598-3608. Epub 2017 Aug 28.

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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October 2017

POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome.

Authors:
Davor Lessel Fuki M Hisama Katalin Szakszon Bidisha Saha Alexander Barrios Sanjuanelo Bonnie A Salbert Pamela D Steele Jennifer Baldwin W Ted Brown Charles Piussan Henri Plauchu Judit Szilvássy Edit Horkay Josef Högel George M Martin Alan J Herr Junko Oshima Christian Kubisch

Hum Mutat 2015 Nov 6;36(11):1070-9. Epub 2015 Aug 6.

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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November 2015

Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?

Authors:
Davor Lessel Bidisha Saha Fuki Hisama Bahar Kaymakamzade Gulay Nurlu Yasemin Gursoy-Özdemir Holger Thiele Peter Nürnberg George M Martin Christian Kubisch Junko Oshima

Am J Med Genet A 2014 Oct 2;164A(10):2510-3. Epub 2014 Jul 2.

Institute of Human Genetics, University of Ulm, Ulm, Germany.

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October 2014

Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts.

Authors:
Bidisha Saha Alexander Cypro George M Martin Junko Oshima

Aging Cell 2014 Jun 5;13(3):573-5. Epub 2014 Feb 5.

Department of Pathology, University of Washington, Seattle, WA, USA.

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June 2014

Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.

Authors:
Bidisha Saha Davor Lessel Sheela Nampoothiri Anuradha S Rao Fuki M Hisama Dincy Peter Chris Bennett Gudrun Nürnberg Peter Nürnberg George M Martin Christian Kubisch Junko Oshima

Mol Genet Genomic Med 2013 May;1(1):7-14

Department of Pathology and Division of Medical Genetics, University of Washington, Seattle, WA, USA.

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May 2013

DNA damage accumulation and TRF2 degradation in atypical Werner syndrome fibroblasts with LMNA mutations.

Authors:
Bidisha Saha Galynn Zitnik Simon Johnson Quyen Nguyen Rosa A Risques George M Martin Junko Oshima

Front Genet 2013 5;4:129. Epub 2013 Jul 5.

Department of Pathology, University of Washington Seattle, WA, USA.

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July 2013

Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.

Authors:
Fuki M Hisama Davor Lessel Dru Leistritz Katrin Friedrich Kim L McBride Matthew T Pastore Gary S Gottesman Bidisha Saha George M Martin Christian Kubisch Junko Oshima

Am J Med Genet A 2011 Dec 7;155A(12):3002-6. Epub 2011 Nov 7.

Medicine, University of Washington, Seattle, Washington 98195-7470, USA.

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December 2011

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.

Authors:
Katrin Friedrich Lin Lee Dru F Leistritz Gudrun Nürnberg Bidisha Saha Fuki M Hisama Daniel K Eyman Davor Lessel Peter Nürnberg Chumei Li María J Garcia-F-Villalta Carolien M Kets Joerg Schmidtke Vítor Tedim Cruz Peter C Van den Akker Joseph Boak Dincy Peter Goli Compoginis Kivanc Cefle Sukru Ozturk Norberto López Theda Wessel Martin Poot P F Ippel Birgit Groff-Kellermann Holger Hoehn George M Martin Christian Kubisch Junko Oshima

Hum Genet 2010 Jul 5;128(1):103-11. Epub 2010 May 5.

Center for Molecular Medicine Cologne, Institute of Human Genetics, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, Cologne, Germany.

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July 2010

Sphingolipid-mediated restoration of Mitf expression and repigmentation in vivo in a mouse model of hair graying.

Authors:
Bidisha Saha Suman Kumar Singh Shampa Mallick Rabindranath Bera Pijush K Datta Mriganka Mandal Syamal Roy Ranjan Bhadra

Pigment Cell Melanoma Res 2009 Apr 22;22(2):205-18. Epub 2009 Jan 22.

Infectious Diseases and Immunology Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata, India.

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April 2009

Activation of the Mitf promoter by lipid-stimulated activation of p38-stress signalling to CREB.

Authors:
Bidisha Saha Suman Kumar Singh Chinmoy Sarkar Rabindranath Bera Jagnyeswar Ratha Desmond J Tobin Ranjan Bhadra

Pigment Cell Res 2006 Dec;19(6):595-605

Department of Cellular Biochemistry, Indian Institute of Chemical Biology, 4, Raja S. C. Mullick Road, Jadavpur, Kolkata 700 032, India.

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December 2006

A sphingolipid rich lipid fraction isolated from attenuated Leishmania donovani promastigote induces apoptosis in mouse and human melanoma cells in vitro.

Authors:
Jagnyeswar Ratha Kajal Nayan Majumdar Sushil Kumar Mandal Rabindranath Bera Chinmoy Sarkar Bidisha Saha Chitra Mandal Krishna Das Saha Ranjan Bhadra

Mol Cell Biochem 2006 Oct 23;290(1-2):113-23. Epub 2006 May 23.

Cellular Biochemistry Division, Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, India.

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October 2006

Transcriptional activation of tyrosinase gene by human placental sphingolipid.

Authors:
Bidisha Saha Suman Kumar Singh Chinmoy Sarkar Shampa Mallick Rabindranath Bera Ranjan Bhadra

Glycoconj J 2006 May;23(3-4):259-68

Cellular Biochemistry Laboratory, Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Jadavpur, Kolkata, 700 032, India.

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May 2006

Human placental protein/peptides stimulate melanin synthesis by enhancing tyrosinase gene expression.

Authors:
Chinmoy Sarkar Suman Kumar Singh Samir Kumar Mandal Bidisha Saha Rabindranath Bera Jagnyeswar Ratha Pijush Kanti Datta Ranjan Bhadra

Mol Cell Biochem 2006 Apr 14;285(1-2):133-42. Epub 2006 Feb 14.

Department of Cellular Biochemistry, Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, 700032, Jadavpur, Kolkata, India.

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April 2006

Human placental lipid induces melanogenesis through p38 MAPK in B16F10 mouse melanoma.

Authors:
Suman Kumar Singh Chinmoy Sarkar Shampa Mallick Bidisha Saha Rabindranath Bera Ranjan Bhadra

Pigment Cell Res 2005 Apr;18(2):113-21

Department of Cellular Biochemistry, Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Jadavpur, Kolkata-700 032, India.

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April 2005

Human placental lipid induces melanogenesis by increasing the expression of tyrosinase and its related proteins in vitro.

Authors:
Shampa Mallick Suman Kumar Singh Chinmoy Sarkar Bidisha Saha Ranjan Bhadra

Pigment Cell Res 2005 Feb;18(1):25-33

Cellular Biochemistry Laboratory, Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Jadavpur, Kolkata 700 032, India.

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February 2005