Molecular genetics of congenital diaphragmatic defects.

Genetic aspects of human congenital diaphragmatic hernia. Clin Genet (2008) 1.81

Congenital diaphragmatic hernia. Orphanet J Rare Dis (2012) 1.40

Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes. Development (2010) 1.26

Imaging of congenital diaphragmatic hernias. Pediatr Radiol (2008) 1.18

Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes. Proc Natl Acad Sci U S A (2012) 1.01

GATA4 deficiency impairs ovarian function in adult mice. Biol Reprod (2011) 0.95

A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia. Am J Med Genet A (2012) 0.91

Congenital diaphragmatic hernia: outcome review of 2,173 surgical repairs in US infants. Pediatr Surg Int (2009) 0.85

Heparan sulfate deficiency disrupts developmental angiogenesis and causes congenital diaphragmatic hernia. J Clin Invest (2013) 0.84

MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development. Hum Mol Genet (2013) 0.83

Minimally invasive surgery for diaphragmatic diseases in neonates and infants. Surg Today (2015) 0.82

Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia. Hum Mol Genet (2015) 0.80

Current technology in the diagnosis of developmentally related lung disorders. Neonatology (2012) 0.76

Laparoscopic transperitoneal repair of pediatric diaphragm eventration using an endostapler device. J Laparoendosc Adv Surg Tech A (2013) 0.75

Neonatal diabetes mellitus and congenital diaphragmatic hernia: coincidence or concurrent etiology? Int J Pediatr Endocrinol (2012) 0.75

Hernia of Morgagni in the Elderly: A Case Report. Cureus (2017) 0.75

Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome. Nat Genet (2003) 11.01

Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome. Science (2006) 10.25

WT-1 is required for early kidney development. Cell (1993) 7.05

Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis. Genes Dev (1997) 6.52

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature (2003) 6.40

Essential role for the c-met receptor in the migration of myogenic precursor cells into the limb bud. Nature (1995) 6.13

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation. Genes Dev (1997) 5.51

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B. Nat Genet (2004) 5.19

TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome. J Clin Invest (2004) 4.85

A membrane receptor for retinol binding protein mediates cellular uptake of vitamin A. Science (2007) 3.73

Fibulin-5 is an elastin-binding protein essential for elastic fibre development in vivo. Nature (2002) 3.60

Inactivation of the lysyl oxidase gene Lox leads to aortic aneurysms, cardiovascular dysfunction, and perinatal death in mice. Circulation (2002) 3.57

Elastin is an essential determinant of arterial morphogenesis. Nature (1998) 3.56

Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants. Development (1994) 3.53

Modeling stochastic gene expression: implications for haploinsufficiency. Proc Natl Acad Sci U S A (1998) 3.49

The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development. Genes Dev (1999) 3.14

Epicardium-derived cells contribute a novel population to the myocardial wall and the atrioventricular cushions. Circ Res (1998) 2.92

FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium. Cell (2000) 2.86

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation. Am J Hum Genet (2007) 2.74

YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis. Development (1999) 2.71

The molecular genetics of Marfan syndrome and related disorders. J Med Genet (2006) 2.45

Haploinsufficiency at the Nkx3.1 locus. A paradigm for stochastic, dosage-sensitive gene regulation during tumor initiation. Cancer Cell (2003) 2.40

Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors. Genes Dev (2001) 2.32

One tissue, two fates: molecular genetic events that underlie testis versus ovary development. Nat Rev Genet (2004) 2.19

Control of skeletal patterning by ephrinB1-EphB interactions. Dev Cell (2003) 2.11

Epithelial-mesenchymal interactions in the developing lung. Annu Rev Physiol (2004) 2.08

Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa. Hum Mol Genet (2002) 2.07

Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome. Proc Natl Acad Sci U S A (2004) 2.01

Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet (2006) 1.99

Essential role of Gab1 for signaling by the c-Met receptor in vivo. J Cell Biol (2000) 1.97

Targeted disruption of fibulin-4 abolishes elastogenesis and causes perinatal lethality in mice. Mol Cell Biol (2006) 1.97

Ephrin signaling in vivo: look both ways. Dev Dyn (2005) 1.93

Lysyl oxidase is required for vascular and diaphragmatic development in mice. J Biol Chem (2002) 1.90

To be or not to be active: the stochastic nature of enhancer action. Bioessays (2000) 1.88

The role of SF/HGF and c-Met in the development of skeletal muscle. Development (1999) 1.85

FOG-2: A novel GATA-family cofactor related to multitype zinc-finger proteins Friend of GATA-1 and U-shaped. Proc Natl Acad Sci U S A (1999) 1.83

Impaired distal airway development in mice lacking elastin. Am J Respir Cell Mol Biol (2000) 1.82

Lysyl oxidase is essential for normal development and function of the respiratory system and for the integrity of elastic and collagen fibers in various tissues. Am J Pathol (2005) 1.79

Gata4 is required for maintenance of postnatal cardiac function and protection from pressure overload-induced heart failure. Proc Natl Acad Sci U S A (2006) 1.73

Capsulin: a novel bHLH transcription factor expressed in epicardial progenitors and mesenchyme of visceral organs. Mech Dev (1998) 1.71

Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS Genet (2005) 1.69

Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development (2002) 1.66

Inadequate lung development and bronchial hyperplasia in mice with a targeted deletion in the Dutt1/Robo1 gene. Proc Natl Acad Sci U S A (2001) 1.65

Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia. Proc Natl Acad Sci U S A (2005) 1.65

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot. Hum Mutat (2006) 1.64

Gonadal differentiation, sex determination and normal Sry expression in mice require direct interaction between transcription partners GATA4 and FOG2. Development (2002) 1.64

Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia. Pediatrics (2005) 1.62

A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries in a large kindred from Qatar. Acta Paediatr (2003) 1.60

A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3. Proc Natl Acad Sci U S A (2003) 1.60

Genetic factors in congenital diaphragmatic hernia. Am J Hum Genet (2007) 1.58

Congenital diaphragmatic hernia, kidney agenesis and cardiac defects associated with Slit3-deficiency in mice. Mech Dev (2003) 1.55

Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization. Am J Hum Genet (2005) 1.52

Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype. Am J Med Genet (1991) 1.49

Control of facial muscle development by MyoR and capsulin. Science (2002) 1.48

Dual-hit hypothesis explains pulmonary hypoplasia in the nitrofen model of congenital diaphragmatic hernia. Am J Pathol (2000) 1.45

Heparan sulfate proteoglycans retain Noggin at the cell surface: a potential mechanism for shaping bone morphogenetic protein gradients. J Biol Chem (2001) 1.43

Aortic aneurysmal disease and cutis laxa caused by defects in the elastin gene. J Med Genet (2005) 1.40

A molecular mechanism for the heparan sulfate dependence of slit-robo signaling. J Biol Chem (2006) 1.37

A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family. J Med Genet (2004) 1.37

Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects. Dev Biol (2006) 1.36

Haploinsufficiency of chicken ovalbumin upstream promoter transcription factor II in female reproduction. Mol Endocrinol (2005) 1.33

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype. Am J Hum Genet (2005) 1.31

Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice. Development (2004) 1.28

The basic helix-loop-helix transcription factor capsulin controls spleen organogenesis. Proc Natl Acad Sci U S A (2000) 1.26

Etiology of congenital diaphragmatic hernia: the retinoid hypothesis. Pediatr Res (2003) 1.25

Diaphragm defects occur in a CDH hernia model independently of myogenesis and lung formation. Am J Physiol Lung Cell Mol Physiol (2002) 1.23

Persistent hypoplasia of the lung after repair of congenital diaphragmatic hernia. Thorax (1976) 1.22

The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males. Am J Hum Genet (2006) 1.22

Where to look for the genes related to diaphragmatic hernia? Genet Couns (2003) 1.20

Mutated MESP2 causes spondylocostal dysostosis in humans. Am J Hum Genet (2004) 1.19

glypican-3 controls cellular responses to Bmp4 in limb patterning and skeletal development. Dev Biol (2000) 1.19

Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature review. Am J Med Genet (1998) 1.18

Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1. J Med Genet (2005) 1.16

Diaphragmatic herniae and translocations involving 8q22 in two patients. J Med Genet (1994) 1.16

Teratogen-induced, dietary and genetic models of congenital diaphragmatic hernia share a common mechanism of pathogenesis. Am J Pathol (2006) 1.14

Gata4 is necessary for normal pulmonary lobar development. Am J Respir Cell Mol Biol (2006) 1.09

Basic helix-loop-helix transcription factor epicardin/capsulin/Pod-1 suppresses differentiation by negative regulation of transcription. J Biol Chem (2002) 1.08

Developmental expression and spermatogenic stage specificity of transcription factors GATA-1 and GATA-4 and their cofactors FOG-1 and FOG-2 in the mouse testis. Eur J Endocrinol (2002) 1.08

Combination of diaphragmatic eventration and microphthalmia/anophthalmia is probably nonrandom. Am J Med Genet (2002) 1.07

Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program. Am J Med Genet A (2005) 1.06

Simpson Golabi Behmel syndrome: progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition. Mol Genet Metab (2001) 1.06

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Hum Mutat (2003) 1.06

Deficiency of distal 8p--report of two cases and review of the literature. Clin Genet (1990) 1.04

Congenital diaphragmatic hernia in WAGR syndrome. Am J Med Genet A (2005) 1.04

Diaphragmatic hernia in Denys-Drash syndrome. Am J Med Genet (1995) 1.03

Genetic disorders of membrane transport. IV. Wilson's disease and Menkes disease. Am J Physiol (1999) 1.02

Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia. Am J Med Genet A (2005) 1.01

Structure of the primordial diaphragm and defects associated with nitrofen-induced CDH. J Appl Physiol (1985) (2000) 1.00

Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet (2005) 1.00

Recurrent congenital diaphragmatic hernia in Ehlers-Danlos syndrome. Cardiovasc Intervent Radiol (2006) 1.00

Cardiovascular malformations in congenital diaphragmatic hernia: human and experimental studies. J Pediatr Surg (1999) 0.99

Cardiac anomalies in patients with congenital diaphragmatic hernia and their prognosis: a report from the Congenital Diaphragmatic Hernia Study Group. J Pediatr Surg (2005) 0.98

Diverse requirements for Notch signalling in mammals. Int J Dev Biol (2002) 0.97

Structural chromosome anomalies in congenital diaphragmatic hernia. Prenat Diagn (1996) 0.96

Congenital posterolateral diaphragmatic hernia: associated malformations. J Pediatr Surg (1988) 0.96

Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia. Eur J Hum Genet (2006) 0.96

Early lung malformations in congenital diaphragmatic hernia. J Pediatr Surg (2000) 0.96

The genetics of congenital diaphragmatic hernia. Semin Perinatol (2005) 0.94

Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature. Prenat Diagn (1998) 0.93

Friend of GATA 2 physically interacts with chicken ovalbumin upstream promoter-TF2 (COUP-TF2) and COUP-TF3 and represses COUP-TF2-dependent activation of the atrial natriuretic factor promoter. J Biol Chem (2001) 0.93

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2. Nat Genet (2007) 3.02

Characteristics of effective school-based substance abuse prevention. Prev Sci (2003) 2.51

Genome sequence of the cellulolytic gliding bacterium Cytophaga hutchinsonii. Appl Environ Microbiol (2007) 2.15

TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements. Blood (2008) 1.99

Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet (2006) 1.99

Heterogeneity of genetic modifiers ensures normal cardiac development. Circulation (2010) 1.94

Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome. J Clin Invest (2008) 1.86

Protective effects of exercise and phosphoinositide 3-kinase(p110alpha) signaling in dilated and hypertrophic cardiomyopathy. Proc Natl Acad Sci U S A (2007) 1.82

Role of the GATA family of transcription factors in endocrine development, function, and disease. Mol Endocrinol (2008) 1.81

Dilated cardiomyopathy resulting from high-level myocardial expression of Cre-recombinase. J Card Fail (2006) 1.79

Cells depleted for RPS19, a protein associated with Diamond Blackfan Anemia, show defects in 18S ribosomal RNA synthesis and small ribosomal subunit production. Blood Cells Mol Dis (2007) 1.68

Genome sequence and analysis of the soil cellulolytic actinomycete Thermobifida fusca YX. J Bacteriol (2007) 1.67

Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome. Development (2007) 1.61

Ovarian granulosa cell tumors in childhood. Pediatr Hematol Oncol (2002) 1.59

Enhanced cardiac PI3Kα signalling mitigates arrhythmogenic electrical remodelling in pathological hypertrophy and heart failure. Cardiovasc Res (2011) 1.53

Transcription factor GATA-6 is expressed in malignant endoderm of pediatric yolk sac tumors and in teratomas. Pediatr Res (2003) 1.52

GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling. Hum Mol Genet (2011) 1.52

P-wave morphology correlation with left atrial volumes assessed by 2-dimensional echocardiography. J Electrocardiol (2005) 1.52

A meta-analysis of alcohol toxicology study findings among homicide victims. Addiction (2010) 1.51

Associations between retinal microvascular abnormalities and declining renal function in the elderly population: the Cardiovascular Health Study. Am J Kidney Dis (2005) 1.50

Effects of follicle-stimulating hormone (FSH) and human chorionic gonadotropin in individuals with an inactivating mutation of the FSH receptor. Fertil Steril (2002) 1.48

Event-chain Monte Carlo algorithms for hard-sphere systems. Phys Rev E Stat Nonlin Soft Matter Phys (2009) 1.41

Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival. Hum Mol Genet (2009) 1.40

Driving sandpiles to criticality and beyond. Phys Rev Lett (2010) 1.38

Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects. Dev Biol (2006) 1.36

Surgical management of renal artery aneurysms. J Vasc Surg (2004) 1.36

Dyskeratosis congenita. FEBS Lett (2010) 1.36

Cutis laxa: a review. J Am Acad Dermatol (2012) 1.32

Fibulin-5 mutations: mechanisms of impaired elastic fiber formation in recessive cutis laxa. Hum Mol Genet (2006) 1.31

Dosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathies. PLoS One (2009) 1.30

Cellulase-xylanase synergy in designer cellulosomes for enhanced degradation of a complex cellulosic substrate. MBio (2010) 1.29

Transcription factors GATA-4 and GATA-6 in normal and neoplastic human gastrointestinal mucosa. BMC Gastroenterol (2008) 1.28

Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene. Blood (2007) 1.26

Regulation and characterization of Thermobifida fusca carbohydrate-binding module proteins E7 and E8. Biotechnol Bioeng (2008) 1.26

Transcription factor GATA-6 is expressed in the endocrine and GATA-4 in the exocrine pancreas. Mol Cell Endocrinol (2004) 1.23

Genetic mosaic analysis reveals that GATA-4 is required for proper differentiation of mouse gastric epithelium. Dev Biol (2002) 1.22

Processivity, substrate binding, and mechanism of cellulose hydrolysis by Thermobifida fusca Cel9A. Appl Environ Microbiol (2007) 1.21

Kinetic studies of Thermobifida fusca Cel9A active site mutant enzymes. Biochemistry (2004) 1.21

New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations. Hum Mutat (2011) 1.20

GATA4 regulates Sertoli cell function and fertility in adult male mice. Mol Cell Endocrinol (2010) 1.20

Recombinant expression and enzymatic characterization of PttCel9A, a KOR homologue from Populus tremula x tremuloides. Biochemistry (2004) 1.17

Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome. J Pediatr Hematol Oncol (2006) 1.15

Conversion of Thermobifida fusca free exoglucanases into cellulosomal components: comparative impact on cellulose-degrading activity. J Biotechnol (2008) 1.15

The FOXL2 C134W mutation is characteristic of adult granulosa cell tumors of the ovary. Mod Pathol (2010) 1.13

Effect of linker length and dockerin position on conversion of a Thermobifida fusca endoglucanase to the cellulosomal mode. Appl Environ Microbiol (2009) 1.13

FOG-2 and GATA-4 Are coexpressed in the mouse ovary and can modulate mullerian-inhibiting substance expression. Biol Reprod (2002) 1.13

A comparison of nLC-ESI-MS/MS and nLC-MALDI-MS/MS for GeLC-based protein identification and iTRAQ-based shotgun quantitative proteomics. J Biomol Tech (2007) 1.11

Homeostatic regulation of electrical excitability in physiological cardiac hypertrophy. J Physiol (2010) 1.10

High GATA-4 expression associates with aggressive behavior, whereas low anti-Müllerian hormone expression associates with growth potential of ovarian granulosa cell tumors. J Clin Endocrinol Metab (2005) 1.09

Mesenteric artery disease in the elderly. J Vasc Surg (2004) 1.09

Developmental expression and spermatogenic stage specificity of transcription factors GATA-1 and GATA-4 and their cofactors FOG-1 and FOG-2 in the mouse testis. Eur J Endocrinol (2002) 1.08

Contribution of a xylan-binding module to the degradation of a complex cellulosic substrate by designer cellulosomes. Appl Environ Microbiol (2010) 1.08

Mouse strain susceptibility to gonadectomy-induced adrenocortical tumor formation correlates with the expression of GATA-4 and luteinizing hormone receptor. Endocrinology (2003) 1.06

GATA-4 is required for sex steroidogenic cell development in the fetal mouse. Dev Dyn (2007) 1.06

TRAIL regulates normal erythroid maturation through an ERK-dependent pathway. Blood (2003) 1.05

Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome. Aging Cell (2007) 1.05

Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis. Hum Mutat (2010) 1.05

GATA-4, GATA-5, and GATA-6 activate the rat liver fatty acid binding protein gene in concert with HNF-1alpha. Am J Physiol Gastrointest Liver Physiol (2004) 1.04

Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation. Circ Cardiovasc Genet (2012) 1.03

Distinct steps of cross-linking, self-association, and maturation of tropoelastin are necessary for elastic fiber formation. J Mol Biol (2007) 1.02

Deconstruction of lignocellulose into soluble sugars by native and designer cellulosomes. MBio (2012) 1.02

Characterization of the molecular interaction between tropoelastin and DANCE/fibulin-5. J Biochem (2008) 1.01

Purification and characterization of Thermobifida fusca xylanase 10B. Can J Microbiol (2004) 1.01

Assembly of xylanases into designer cellulosomes promotes efficient hydrolysis of the xylan component of a natural recalcitrant cellulosic substrate. MBio (2011) 1.01

Differential expression of GATA-4 and GATA-6 in fetal and adult mouse and human adrenal tissue. Endocrinology (2002) 1.01

Inflammatory destruction of elastic fibers in acquired cutis laxa is associated with missense alleles in the elastin and fibulin-5 genes. J Invest Dermatol (2006) 1.00

Mechanisms of emphysema in autosomal dominant cutis laxa. Matrix Biol (2010) 0.99

Processivity, synergism, and substrate specificity of Thermobifida fusca Cel6B. Appl Environ Microbiol (2009) 0.98

Dyskeratosis congenita and telomerase. Curr Opin Pediatr (2004) 0.98

A tomato endo-beta-1,4-glucanase, SlCel9C1, represents a distinct subclass with a new family of carbohydrate binding modules (CBM49). J Biol Chem (2007) 0.98

GATA-4 regulates Bcl-2 expression in ovarian granulosa cell tumors. Endocrinology (2008) 0.98

GATA-4:FOG interactions regulate gastric epithelial development in the mouse. Dev Dyn (2005) 0.98

The complexity of elastic fibre biogenesis in the skin--a perspective to the clinical heterogeneity of cutis laxa. Exp Dermatol (2012) 0.97

Glycoside hydrolases: catalytic base/nucleophile diversity. Biotechnol Bioeng (2010) 0.97

TINF2 mutations in children with severe aplastic anemia. Pediatr Blood Cancer (2009) 0.97

Gonadotropin-induced adrenocortical neoplasia in NU/J nude mice. Endocrinology (2005) 0.96

Human telomerase RNA mutations and bone marrow failure. Lancet (2003) 0.96

GATA4 deficiency impairs ovarian function in adult mice. Biol Reprod (2011) 0.95

Pilocytic astrocytoma in a child with Noonan syndrome. Pediatr Blood Cancer (2009) 0.95

Cloning, expression and characterization of a family-74 xyloglucanase from Thermobifida fusca. Eur J Biochem (2003) 0.95