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Author Details

Farid F Chehab
University of California san francisco
1984
65
30
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
33375775Molecular and phenotypic diversity of CBL-mutated juvenile myelomonocytic leukemia.Haematologica2022
34481221Outcomes of activated prothrombin complex concentrate for direct Xa inhibitor bleeding.Thromb Res2021
30532056PAX5, NOTCH3, CBFB, and ACD drive an activated RAS pathway and monosomy 7 to B-ALL and AML in donor cell leukemia.Bone Marrow Transplant2019
31347788Molecular assessment of pretransplant chemotherapy in the treatment of juvenile myelomonocytic leukemia.Pediatr Blood Cancer2019
29718007Upregulation of cholesterol 24-hydroxylase following hypoxia-ischemia in neonatal mouse brain.Pediatr Res2018
29259179Genome-wide DNA methylation is predictive of outcome in juvenile myelomonocytic leukemia.Nat Commun2017
26511402Novel TKI-resistant BCR-ABL1 gatekeeper residue mutations retain in vitro sensitivity to axitinib.Leukemia2016
24353279FoxO4 interacts with the sterol regulatory factor SREBP2 and the hypoxia inducible factor HIF2α at the CYP51 promoter.J Lipid Res2014
25233259First report of a deletion encompassing an entire exon in the homogentisate 1,2-dioxygenase gene causing alkaptonuria.PLoS One2014
2511820720 years of leptin: leptin and reproduction: past milestones, present undertakings, and future endeavors.J Endocrinol2014
23300646Duplication of C7orf58, WNT16 and FAM3C in an obese female with a t(7;22)(q32.1;q11.2) chromosomal translocation and clinical features resembling Coffin-Siris Syndrome.PLoS One2012
21390308Homozygous deletion of six olfactory receptor genes in a subset of individuals with Beta-thalassemia.PLoS One2011
20037138Effects of FoxO4 overexpression on cholesterol biosynthesis, triacylglycerol accumulation, and glucose uptake.J Lipid Res2010
19410631Overexpression of the transcription factor Foxo4 is associated with rapid glucose clearance.Mol Cell Endocrinol2009
18202137Obesity and lipodystrophy--where do the circles intersect?Endocrinology2008
16761284Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male.Am J Med Genet A2006
17064660Deletion of the serotonin 2c receptor from transgenic mice overexpressing leptin does not affect their lipodystrophy but exacerbates their diet-induced obesity.Biochem Biophys Res Commun2006
14749505The use of animal models to dissect the biology of leptin.Recent Prog Horm Res2004
12810541Hyperleptinemia precipitates diet-induced obesity in transgenic mice overexpressing leptin.Endocrinology2003
14651995Overexpression of leptin in transgenic mice leads to decreased basal lipolysis, PKA activity, and perilipin levels.Biochem Biophys Res Commun2003
12403083Leptin and reproduction.Nutr Rev2002
11145598Transgenic mice overexpressing leptin accumulate adipose mass at an older, but not younger, age.Endocrinology2001
11459786Leptin-deficient mice backcrossed to the BALB/cJ genetic background have reduced adiposity, enhanced fertility, normal body temperature, and severe diabetes.Endocrinology2001
10918637Leptin as a regulator of adipose mass and reproduction.Trends Pharmacol Sci2000
9927300Effect of the genetic background on the reproduction of leptin-deficient obese mice.Endocrinology1999
9832467Leptin is not necessary for gestation and parturition but regulates maternal nutrition via a leptin resistance state.Endocrinology1998
9048626Leptin treatment rescues the sterility of genetically obese ob/ob males.Endocrinology1997
9288714The reproductive side of leptin.Nat Med1997
9322076Is Hb A2 elevated in adults with sickle-alpha-thalassemia (beta(S)/beta(S); -alpha/-alpha)?Hemoglobin1997
9581539Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.Biochem J1997
8974400Early onset of reproductive function in normal female mice treated with leptin.Science1997
9056561Molecular basis of asymptomatic beta-thalassemia major in an African American individual.Am J Med Genet1997
9002673Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection method.Hum Mol Genet1997
8589726Correction of the sterility defect in homozygous obese female mice by treatment with the human recombinant leptin.Nat Genet1996
8673906A broader role for leptin.Nat Med1996
8788995Comparison of PCR detection of mecA with standard susceptibility testing methods to determine methicillin resistance in coagulase-negative staphylococci.J Clin Microbiol1996
8889595New frameshift mutation, insertion of A, at codon 95 of the beta-globin gene causes beta-thalassemia in two Vietnamese families.Hum Mutat1996
7485338Detection of viral deoxyribonucleic acid in the amniotic fluid of low-risk pregnancies by polymerase chain reaction.Am J Obstet Gynecol1995
7627189A 31-mutation assay for cystic fibrosis testing in the clinical molecular diagnostics laboratory.Hum Mutat1995
7545404Methylation status of CpG sites in the mouse and human CFTR promoters.DNA Cell Biol1995
7526924Analysis of the mouse and rat CFTR promoter regions.Hum Mol Genet1994
8081396A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband.Hum Mutat1994
8118512Analysis of gene sequences by hybridization of PCR-amplified DNA to covalently bound oligonucleotide probes. The reverse dot blot method.Methods Mol Biol1994
8118466Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks.Hum Mutat1994
7913578Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.Am J Hum Genet1994
8417793Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily.Blood1993
8257984Molecular diagnostics: past, present, and future.Hum Mutat1993
1479898Amplification and detection of specific DNA sequences with fluorescent PCR primers: application to delta F508 mutation in cystic fibrosis.Methods Enzymol1992
1583123DNA amplification and reverse dot blot hybridization for detection and identification of mycobacteria to the species level in the clinical laboratory.J Clin Microbiol1992
1587526Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening.Hum Genet1992
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Collaborators

University of Washington
Co-authored papers 3
Cardiovascular Research Institute, University of California at San Francisco
Co-authored papers 3
University of California San Francisco
Co-authored papers 2
12224University of California san francisco
Co-authored papers 2
University of California San Francisco
Co-authored papers 1
University of California San Francisco
Co-authored papers 1
Co-authored papers 1
University of California san francisco
Co-authored papers 1
Instituto de Salud Carlos III
Co-authored papers 1
University of California san francisco
Co-authored papers 1
is executive director of clinical development at TerSera Therapeutics
Co-authored papers 1
Benioff Children's Hospitals, University of California san francisco
Co-authored papers 1
Co-authored papers 1
University of California san francisco
Co-authored papers 1
University of California san francisco
Co-authored papers 1
Children's Hospital Oakland Research Institute
Co-authored papers 1
University of California San Francisco
Co-authored papers 1
Benioff Children's Hospital, University of California san francisco
Co-authored papers 1
Laval University
Co-authored papers 1
University of California san francisco
Co-authored papers 1
Emory School of Medicine
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
Co-authored papers 1
Schools of Pharmacy and Medicine, University of California san francisco
Co-authored papers 1
German Cancer Research Center
Co-authored papers 1
Co-authored papers 1