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21 results for author:"Drumm M.L." in Literature citations

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Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection.

Bonfield T.L., Hodges C.A., Cotton C.U., Drumm M.L.

J. Leukoc. Biol. 92:1111-1122(2012) · Mapped (8)

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.

Sun L., Rommens J.M., Corvol H., Li W., Li X., Chiang T.A., Lin F., Dorfman R., Busson P.F., Parekh R.V. et al.

Nat. Genet. 44:562-569(2012) · Mapped (6)

Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.

Henderson L.B., Doshi V.K., Blackman S.M., Naughton K.M., Pace R.G., Moskovitz J., Knowles M.R., Durie P.R., Drumm M.L., Cutting G.R.

PLoS Genet. 8:e1002580-e1002580(2012) · Mapped (8)

Phospholipase C-beta3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells.

Bezzerri V., d'Adamo P., Rimessi A., Lanzara C., Crovella S., Nicolis E., Tamanini A., Athanasakis E., Tebon M., Bisoffi G. et al.

J. Immunol. 186:4946-4958(2011) · Mapped (4)

EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity.

Darrah R., McKone E., O'Connor C., Rodgers C., Genatossio A., McNamara S., Gibson R., Stuart Elborn J., Ennis M., Gallagher C.G. et al.

Physiol. Genomics 41:71-77(2010) · Mapped (23)

Genetic modifiers of liver disease in cystic fibrosis.

Bartlett J.R., Friedman K.J., Ling S.C., Pace R.G., Bell S.C., Bourke B., Castaldo G., Castellani C., Cipolli M., Colombo C. et al.

JAMA 302:1076-1083(2009) · Mapped (23)

A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosis.

Blackman S.M., Hsu S., Ritter S.E., Naughton K.M., Wright F.A., Drumm M.L., Knowles M.R., Cutting G.R.

Diabetologia 52:1858-1865(2009) · Mapped (32)

Loss of CFTR results in reduction of histone deacetylase 2 in airway epithelial cells.

Bartling T.R., Drumm M.L.

Am. J. Physiol. Lung Cell Mol. Physiol. 297:L35-43(2009) · Mapped (49)

Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease.

Gu Y., Harley I.T., Henderson L.B., Aronow B.J., Vietor I., Huber L.A., Harley J.B., Kilpatrick J.R., Langefeld C.D., Williams A.H. et al.

Nature 458:1039-1042(2009) · Mapped (7)

Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.

Taylor-Cousar J.L., Zariwala M.A., Burch L.H., Pace R.G., Drumm M.L., Calloway H., Fan H., Weston B.W., Wright F.A., Knowles M.R.

PLoS ONE 4:e4270-e4270(2009) · Mapped (135)

Generation of a conditional null allele for Cftr in mice.

Hodges C.A., Cotton C.U., Palmert M.R., Drumm M.L.

Genesis 46:546-552(2008) · Mapped (50)

Oxidative stress causes IL8 promoter hyperacetylation in cystic fibrosis airway cell models.

Bartling T.R., Drumm M.L.

Am. J. Respir. Cell Mol. Biol. 40:58-65(2009) · Mapped (1)

Modulation of cystic fibrosis lung disease by variants in interleukin-8.

Hillian A.D., Londono D., Dunn J.M., Goddard K.A., Pace R.G., Knowles M.R., Drumm M.L.

Genes Immun. 9:501-508(2008) · Mapped (12)

Infertility in females with cystic fibrosis is multifactorial: evidence from mouse models.

Hodges C.A., Palmert M.R., Drumm M.L.

Endocrinology 149:2790-2797(2008) · Mapped (5)

The cystic fibrosis transmembrane conductance regulator (Cftr) modulates the timing of puberty in mice.

Jin R., Hodges C.A., Drumm M.L., Palmert M.R.

J. Med. Genet. 43:e29-e29(2006) · Mapped (5)

Genetic modifiers of lung disease in cystic fibrosis.

Drumm M.L., Konstan M.W., Schluchter M.D., Handler A., Pace R., Zou F., Zariwala M., Fargo D., Xu A., Dunn J.M. et al.

N. Engl. J. Med. 353:1443-1453(2005) · Mapped (54)

Beta 2 adrenergic receptor polymorphisms in cystic fibrosis.

Hart M.A., Konstan M.W., Darrah R.J., Schluchter M.D., Storfer-Isser A., Xue L., Londono D., Goddard K.A., Drumm M.L.

Pediatr. Pulmonol. 39:544-550(2005) · Mapped (2)

Role of Cftr genotype in the response to chronic Pseudomonas aeruginosa lung infection in mice.

van Heeckeren A.M., Schluchter M.D., Drumm M.L., Davis P.B.

Am. J. Physiol. Lung Cell Mol. Physiol. 287:L944-52(2004) · Mapped (7)

Stimulation of cystic fibrosis transmembrane conductance regulator-dependent short-circuit currents across DeltaF508 murine intestines.

Steagall W.K., Drumm M.L.

Gastroenterology 116:1379-1388(1999) · Mapped (5)

Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells.

Kelley T.J., Drumm M.L.

J. Clin. Invest. 102:1200-1207(1998) · Mapped (7)

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

Riordan J.R., Rommens J.M., Kerem B., Alon N., Rozmahel R., Grzelczak Z., Zielenski J., Lok S., Plavsic N., Chou J.-L. et al.

Science 245:1066-1073(1989) · UniProtKB (1) · Mapped (5)

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