Farida Latif - AILBRY - Article Search

Results for 'Farida Latif' :

Molecular genetic analysis of the 3p — syndrome

Publication Year: 1994

DOI: https://doi.org/10.1093/hmg/3.6.903

Abstract:

Authors:
- Maude E. Phipps
- Farida Latif
- Amanda Prowse
- Stewart J. Payne
- Jeanne Dietz‐Band
- Margaret Leversha
- Nabeel A. Affara
- Anthony T. Moore
- John Tolmie
- Albert Schinzel
- Michael I. Lerman
- M.A. Ferguson‐Smith
- Eamonn R. Maher
CALL gene is haploinsufficient in a 3p? syndrome patient

Publication Year: 1999

DOI: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5<482::aid-ajmg15>3.0.co;2-l

Abstract:

Authors:
- Debora Angeloni
- Noralane M. Lindor
- Svetlana Pack
- Farida Latif
- Minghui Wei
- Michael I. Lerman
Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3:D3S587; D3S1317; D3S1435

Publication Year: 1993

DOI: https://doi.org/10.1093/hmg/2.8.1326

Abstract:

Authors:
- Hua Li
- Laura S. Schmidt
- Fuh-Mei C. Duh
- Minghui Wei
- Farida Latif
- Thomas Stackhouse
- Michael I. Lerman
- Berton Zbar
- Kálmán Tory
Germline SDHB Mutations and Familial Renal Cell Carcinoma

Publication Year: 2008

DOI: https://doi.org/10.1093/jnci/djn254

Abstract:

Authors:
- Christopher J. Ricketts
- Emma R. Woodward
- Pip Killick
- Mark R. Morris
- Dewi Astuti
- Farida Latif
- Eamonn R. Maher
Germline SDHD mutation in familial phaeochromocytoma

Publication Year: 2001

DOI: https://doi.org/10.1016/s0140-6736(00)04378-6

Abstract:

Authors:
- Dewi Astuti
- Fiona Douglas
- Thomas W. J. Lennard
- Irene A. Aligianis
- Emma R. Woodward
- D. Gareth Evans
- Charis Eng
- Farida Latif
- Eamonn R. Maher
The VHL tumour-suppressor gene paradigm

Publication Year: 1998

DOI: https://doi.org/10.1016/s0168-9525(98)01558-3

Abstract:

Authors:
- William G. Kaelin
- Eamonn R. Maher
Role of the Ras-Association Domain Family 1 Tumor Suppressor Gene in Human Cancers

Publication Year: 2005

DOI: https://doi.org/10.1158/0008-5472.can-04-4088

Abstract:

Authors:
- Angelo Agathanggelou
- Wendy N. Cooper
- Farida Latif
Ratio of donor kidney weight to recipient bodyweight as an index of graft function

Publication Year: 2001

DOI: https://doi.org/10.1016/s0140-6736(00)04377-4

Abstract:

Authors:
- Yu Seun Kim
- Jang Il Moon
- Dong Kee Kim
- Soon Il Kim
- Kiil Park
Different Mechanisms of Aralkylation of Adenosine at the 1- and N6-Positions

Publication Year: 1995

DOI: https://doi.org/10.1021/tx00045a010

Abstract:

Authors:
- Chengyi Qian
- Anthony Dipple
Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes

Publication Year: 2000

DOI: https://doi.org/10.1136/jmg.37.5.348

Abstract:

Authors:
- Emma R. Woodward
Slit-2 Induces a Tumor-suppressive Effect by Regulating β-Catenin in Breast Cancer Cells

Publication Year: 2008

DOI: https://doi.org/10.1074/jbc.m800679200

Abstract:

Authors:
- Anil Prasad
- Vikram Paruchuri
- Anju Preet
- Farida Latif
- Ramesh K. Ganju
Cell Cycle Restriction Is More Important Than Apoptosis Induction for RASSF1A Protein Tumor Suppression

Publication Year: 2014

DOI: https://doi.org/10.1074/jbc.m114.609537

Abstract:

Authors:
- Howard Donninger
- Jennifer Clark
- Megan K. Monaghan
- Marianne Schmidt
- Michele D. Vos
- Geoffrey Clark
5‐Methylcytosine—The Fifth Base of DNA: The Fifth Wheel on a Car or a Highly Promising Diagnostic and Therapeutic Target in Cancer?

Publication Year: 2007

DOI: https://doi.org/10.1155/2007/860404

Abstract:

Authors:
- Martin Widschwendter
Molecular pathology of von Hippel–Lindau disease and the <i>VHL</i> tumour suppressor gene

Publication Year: 2001

DOI: https://doi.org/10.1017/s1462399401002654

Abstract:

Authors:
- Frances M. Richards
RASSF Family Proteins

Publication Year: 2012

DOI: https://doi.org/10.1155/2012/938916

Abstract:

Authors:
- Geoffrey Clark
- Shairaz Baksh
- Farida Latif
- Dae‐Sik Lim

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AILBRY - Article Search

Results for 'Farida Latif' :

Molecular genetic analysis of the 3p — syndrome

CALL gene is haploinsufficient in a 3p? syndrome patient

Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3:D3S587; D3S1317; D3S1435

Germline SDHB Mutations and Familial Renal Cell Carcinoma

Germline SDHD mutation in familial phaeochromocytoma

The VHL tumour-suppressor gene paradigm

Role of the Ras-Association Domain Family 1 Tumor Suppressor Gene in Human Cancers

Ratio of donor kidney weight to recipient bodyweight as an index of graft function

Different Mechanisms of Aralkylation of Adenosine at the 1- and N6-Positions

Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes

Slit-2 Induces a Tumor-suppressive Effect by Regulating β-Catenin in Breast Cancer Cells

Cell Cycle Restriction Is More Important Than Apoptosis Induction for RASSF1A Protein Tumor Suppression

5‐Methylcytosine—The Fifth Base of DNA: The Fifth Wheel on a Car or a Highly Promising Diagnostic and Therapeutic Target in Cancer?

Molecular pathology of von Hippel–Lindau disease and the <i>VHL</i> tumour suppressor gene

RASSF Family Proteins

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