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23 results for author:"Chan Y.M."Drop in Literature Citations

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GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism.

Chan Y.M., de Guillebon A., Lang-Muritano M., Plummer L., Cerrato F., Tsiaras S., Gaspert A., Lavoie H.B., Wu C.H., Crowley W.F. Jr. et al.

Proc. Natl. Acad. Sci. U.S.A. 106:11703-11708(2009) · Mapped (1)

EDN1 Lys198Asn is associated with diabetic retinopathy in type 2 diabetes.

Li H., Louey J.W., Choy K.W., Liu D.T., Chan W.M., Chan Y.M., Fung N.S., Fan B.J., Baum L., Chan J.C. et al.

Mol. Vis. 14:1698-1704(2008) · Mapped (31)

Transition from insulin to glyburide in a 4-month-old girl with neonatal diabetes mellitus caused by a mutation in KCNJ11.

Chan Y.M., Laffel L.M.

Pediatr Diabetes 8:235-238(2007) · Mapped (4)

Kiss1-/- mice exhibit more variable hypogonadism than Gpr54-/-mice.

Lapatto R., Pallais J.C., Zhang D., Chan Y.M., Mahan A., Cerrato F., Le W.W., Hoffman G.E., Seminara S.B.

Endocrinology 148:4927-4936(2007) · Mapped (6)

The 16 kDa subunit of vacuolar H+-ATPase is a novel sarcoglycan-interacting protein.

Chen J., Skinner M.A., Shi W., Yu Q.C., Wildeman A.G., Chan Y.M.

Biochim. Biophys. Acta 1772:570-579(2007) · Mapped (4)

MLH1 -93G>A promoter polymorphism and the risk of microsatellite-unstable colorectal cancer.

Raptis S., Mrkonjic M., Green R.C., Pethe V.V., Monga N., Chan Y.M., Daftary D., Dicks E., Younghusband B.H., Parfrey P.S. et al.

J. Natl. Cancer Inst. 99:463-474(2007) · Mapped (30)

Identification of functional domains in sarcoglycans essential for their interaction and plasma membrane targeting.

Chen J., Shi W., Zhang Y., Sokol R., Cai H., Lun M., Moore B.F., Farber M.J., Stepanchick J.S., Bonnemann C.G. et al.

Exp. Cell Res. 312:1610-1625(2006) · Mapped (6)

The sequence and analysis of duplication-rich human chromosome 16.

Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M. et al.

Nature 432:988-994(2004) · UniProtKB (638)

The DNA sequence and comparative analysis of human chromosome 5.

Schmutz J., Martin J., Terry A., Couronne O., Grimwood J., Lowry S., Gordon L.A., Scott D., Xie G., Huang W. et al.

Nature 431:268-274(2004) · UniProtKB (616)

The DNA sequence and biology of human chromosome 19.

Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M. et al.

Nature 428:529-535(2004) · UniProtKB (1,180)

Erythropoietin modulates calcium influx through TRPC2.

Chu X., Cheung J.Y., Barber D.L., Birnbaumer L., Rothblum L.I., Conrad K., Abrasonis V., Chan Y.M., Stahl R., Carey D.J. et al.

J. Biol. Chem. 277:34375-34382(2002) · Mapped (9)

A Gain-of-Function Screen for Genes That Affect the Development of the Drosophila Adult External Sensory Organ.

Abdelilah-Seyfried S., Chan Y.M., Zeng C., Justice N.J., Younger-Shepherd S., Sharp L.E., Barbel S., Meadows S.A., Jan L.Y., Jan Y.N.

Genetics 157:455-456(2001) · Mapped (19)

A gain-of-function screen for genes that affect the development of the Drosophila adult external sensory organ.

Abdelilah-Seyfried S., Chan Y.M., Zeng C., Justice N.J., Younger-Shepherd S., Sharp L.E., Barbel S., Meadows S.A., Jan L.Y., Jan Y.N.

Genetics 155:733-752(2000) · Mapped (159)

Filamin 2 (FLN2): a muscle-specific sarcoglycan interacting protein.

Thompson T.G., Chan Y.-M., Hack A.A., Brosius M., Rajala M., Lidov H.G.W., McNally E.M., Watkins S., Kunkel L.M.

J. Cell Biol. 148:115-126(2000) · UniProtKB (3)

Conservation of neurogenic genes and mechanisms.

Chan Y.M., Jan Y.N.

Curr. Opin. Neurobiol. 9:582-588(1999) · Mapped (33)

Presenilins, processing of beta-amyloid precursor protein, and notch signaling.

Chan Y.M., Jan Y.N.

Neuron 23:201-204(1999) · Mapped (8)

Molecular organization of sarcoglycan complex in mouse myotubes in culture.

Chan Y.-M., Boennemann C.G., Lidov H.G.W., Kunkel L.M.

J. Cell Biol. 143:2033-2044(1998) · UniProtKB (5)

The Drosophila LIM-only gene, dLMO, is mutated in Beadex alleles and might represent an evolutionarily conserved function in appendage development.

Zeng C., Justice N.J., Abdelilah S., Chan Y.M., Jan L.Y., Jan Y.N.

Proc. Natl. Acad. Sci. U.S.A. 95:10637-10642(1998) · Mapped (7)

Miranda as a multidomain adapter linking apically localized Inscuteable and basally localized Staufen and Prospero during asymmetric cell division in Drosophila.

Shen C.P., Knoblich J.A., Chan Y.M., Jiang M.M., Jan L.Y., Jan Y.N.

Genes Dev. 12:1837-1846(1998) · Mapped (14)

Genetic analysis of a severe case of Dowling-Meara epidermolysis bullosa simplex.

Chan Y.-M., Cheng J., Gedde-Dahl T. Jr., Niemi K.M., Fuchs E.

J. Invest. Dermatol. 106:327-334(1996) · UniProtKB (1)

The genetic basis of Weber-Cockayne epidermolysis bullosa simplex.

Chan Y.-M., Yu Q.-C., Fine J.-D., Fuchs E.

Proc. Natl. Acad. Sci. U.S.A. 90:7414-7418(1993) · UniProtKB (1)

Genetic and clinical mosaicism in a type of epidermal nevus.

Paller A.S., Syder A.J., Chan Y.-M., Yu Q.-C., Hutton M.E., Tadini G., Fuchs E.

N. Engl. J. Med. 331:1408-1415(1994) · UniProtKB (1)

Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex.

Chan Y.-M., Yu Q.-C., LeBlanc-Straceski J., Christiano A., Pulkkinen L., Kucherlapati R.S., Uitto J., Fuchs E.

J. Cell Sci. 107:765-774(1994) · UniProtKB (1)

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