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Journal of Medical Genetics
|
September 24, 2024
A novel pathogenic germline chromosome 3 inversion in von Hippel-Lindau disease
Cathy D Vocke, Christopher J Ricketts, Svetlana Pack, et al.
Scientific Reports
|
June 10, 2021
Real-Time insight into in vivo redox status utilizing hyperpolarized [1-<sup>13</sup>C] N-acetyl cysteine
Kazutoshi Yamamoto, Ana Opina, Deepak Sail, et al.
Cancer Cell
|
September 3, 2002
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome
Michael L Nickerson, Michelle B Warren, Jorge R Toro, et al.
Urologic Oncology
|
August 23, 2025
Renal surgery following HIF-2α antagonist therapy: Surgical indications, outcomes and growth kinetics
Daniel Nethala, Braden Millan, Jason Hyman, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 1, 2018
Therapeutic Targeting of TFE3/IRS-1/PI3K/mTOR Axis in Translocation Renal Cell Carcinoma
Nur P Damayanti, Justin A Budka, Heba W Z Khella, et al.
Nature Chemical Biology
|
February 6, 2019
A chemoproteomic portrait of the oncometabolite fumarate
Rhushikesh A Kulkarni, Daniel W Bak, Darmood Wei, et al.
Cancer
|
April 30, 2009
Innovations and challenges in renal cancer: summary statement from the Third Cambridge Conference
Michael B Atkins, Ronald M Bukowski, Bernard J Escudier, et al.
Biochemical and Biophysical Research Communications
|
December 7, 2019
FLCN alteration drives metabolic reprogramming towards nucleotide synthesis and cyst formation in salivary gland
Yasuhiro Isono, Mitsuko Furuya, Tatsu Kuwahara, et al.
Blood
|
June 20, 2012
The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development
Masaya Baba, Jonathan R Keller, Hong-Wei Sun, et al.
Cancer Biology & Therapy
|
January 22, 2005
Altered gene expression in phenotypically normal renal cells from carriers of tumor suppressor gene mutations
Radka Stoyanova, Margie L Clapper, Alfonso Bellacosa, et al.
Page
of 49
Search research articles
Search
Showing results (421-430 of 487) with videos related to
Sort By:
Page
of 49
Journal of Medical Genetics
|
September 24, 2024
A novel pathogenic germline chromosome 3 inversion in von Hippel-Lindau disease
Cathy D Vocke, Christopher J Ricketts, Svetlana Pack, et al.
Scientific Reports
|
June 10, 2021
Real-Time insight into in vivo redox status utilizing hyperpolarized [1-<sup>13</sup>C] N-acetyl cysteine
Kazutoshi Yamamoto, Ana Opina, Deepak Sail, et al.
Cancer Cell
|
September 3, 2002
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome
Michael L Nickerson, Michelle B Warren, Jorge R Toro, et al.
Urologic Oncology
|
August 23, 2025
Renal surgery following HIF-2α antagonist therapy: Surgical indications, outcomes and growth kinetics
Daniel Nethala, Braden Millan, Jason Hyman, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 1, 2018
Therapeutic Targeting of TFE3/IRS-1/PI3K/mTOR Axis in Translocation Renal Cell Carcinoma
Nur P Damayanti, Justin A Budka, Heba W Z Khella, et al.
Nature Chemical Biology
|
February 6, 2019
A chemoproteomic portrait of the oncometabolite fumarate
Rhushikesh A Kulkarni, Daniel W Bak, Darmood Wei, et al.
Cancer
|
April 30, 2009
Innovations and challenges in renal cancer: summary statement from the Third Cambridge Conference
Michael B Atkins, Ronald M Bukowski, Bernard J Escudier, et al.
Biochemical and Biophysical Research Communications
|
December 7, 2019
FLCN alteration drives metabolic reprogramming towards nucleotide synthesis and cyst formation in salivary gland
Yasuhiro Isono, Mitsuko Furuya, Tatsu Kuwahara, et al.
Blood
|
June 20, 2012
The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dubé syndrome is required for murine B-cell development
Masaya Baba, Jonathan R Keller, Hong-Wei Sun, et al.
Cancer Biology & Therapy
|
January 22, 2005
Altered gene expression in phenotypically normal renal cells from carriers of tumor suppressor gene mutations
Radka Stoyanova, Margie L Clapper, Alfonso Bellacosa, et al.
Page
of 49