1 rstanding of the genetic alterations causing
hereditary forms and the increasing sensitivity of bioch
2 By contrast, in the
hereditary form,
ApoE immunoreactivity occurred on mater
3 Adult presentations of known
hereditary forms are often accompanied by other organ in
4 e chemotactic factor 2 amyloidosis, but rare
hereditary forms can also involve the kidneys.
5 disease phenotype between transmissable and
hereditary forms could result from interactions between
6 In the United States, the
hereditary form disproportionately afflicts black Americ
7 f rickets, other types of rickets, including
hereditary forms,
must be considered in the differential
8 an attempt to clarify the pathology of this
hereditary form of Alzheimer's disease and to determine
9 hyretin familial amyloid polyneuropathy is a
hereditary form of amyloidosis characterized by sensorim
10 Cystatin C amyloids cause a
hereditary form of cerebral amyloid angiopathy whilst cy
11 colorectal cancer (HNPCC) is the most common
hereditary form of colon cancer.
12 observed in tumor cells of patients having a
hereditary form of colon cancer.
13 Lynch syndrome is the most common
hereditary form of colorectal cancer (CRC).
14 gene encoding glucokinase (GCK) cause a mild
hereditary form of diabetes termed maturity-onset diabet
15 The primary or
hereditary form of distal renal tubular acidosis (dRTA),
16 Here, we report a
hereditary form of DSPD associated with a dominant codin
17 CRT-III component) that is associated with a
hereditary form of frontotemporal dementia (FTD3) disrup
18 members, WNK1 and WNK4 have been linked to a
hereditary form of hypertension, pseudohypoaldosteronism
19 ular salt levels and is directly linked to a
hereditary form of hypertension.
20 polyposis coli tumor suppressor gene cause a
hereditary form of intestinal tumorigenesis in both mice
21 is defective in Stargardt disease, a common
hereditary form of macular dystrophy.
22 In contrast to the
hereditary form of medullary thyroid carcinoma (MTC), li
23 Cubulin mutations cause a
hereditary form of megaloblastic anemia secondary to vit
24 fibrils is associated with a rare but fatal
hereditary form of nonneuropathic systemic amyloidosis.
25 The
hereditary form of retinoblastoma (Rb) is associated wit
26 ate into amyloid fibrils observed in a fatal
hereditary form of systemic amyloidosis.
27 ple prostate cancer loci responsible for the
hereditary form of this common and complex disease and t
28 n suggested that known genetic causes of the
hereditary form of this disease account for upwards of 1
29 ncluding Lynch syndrome as the most frequent
hereditary form of this disease.
30 MET is the gene for the
hereditary form of type 1 papillary renal carcinoma and
31 itary leiomyomatosis renal cell carcinoma, a
hereditary form of type 2 papillary renal carcinoma, is
32 The majority of
hereditary forms of breast and ovarian cancer can be acc
33 A1, a tumor suppressor protein implicated in
hereditary forms of breast and ovarian cancer, is transc
34 tumor suppressor that has been implicated in
hereditary forms of breast and ovarian cancer.
35 The common
hereditary forms of breast cancer have been largely attr
36 aling, are responsible for most sporadic and
hereditary forms of colorectal cancer (CRC).
37 nd multiple myosin genes are associated with
hereditary forms of deafness.
38 rom animal studies that attempt to mimic the
hereditary forms of early-onset dementia.
39 Dermatopathology textbooks include
hereditary forms of EB among the "cell-poor" list of sub
40 Hereditary forms of FSGS have been linked to mutations i
41 ibits diurnal variation in both acquired and
hereditary forms of heart disease, but the molecular bas
42 Hereditary forms of human prion disease are linked to sp
43 (ii) human DLG1 mutations may contribute to
hereditary forms of hydronephrosis.
44 toimmune gastritis, Helicobacter pylori, and
hereditary forms of IDA is recommended.
45 s an appropriate target for investigation of
hereditary forms of iminoaciduria in man.
46 patients at-risk for the development of the
hereditary forms of medullary thyroid carcinoma has simp
47 function, including all six genes mutated in
hereditary forms of monogenic type 2 diabetes.
48 finger E3 ubiquitin ligase also involved in
hereditary forms of muscular dystrophy, NPHP7/Glis2 is a
49 yrosine kinase domain of MET in sporadic and
hereditary forms of papillary kidney cancer.
50 derstanding the function of genes mutated in
hereditary forms of Parkinson's disease yields insight i
51 een linked to early onset autosomal dominant
hereditary forms of PD, and have been shown to affect th
52 other familial mutations, indicate that some
hereditary forms of prion disease cannot be rationalized
53 ave been shown recently to co-segregate with
hereditary forms of progressive kidney failure.
54 Hereditary forms of the disease are linked to specific m
55 Two autosomal dominant
hereditary forms of the disease, familial adenomatous po
56 However, the discovery of genes mutated in
hereditary forms of these enigmatic diseases has additio
57 Hereditary forms of Wilms arise from developmentally arr
58 araganglial system, with a high frequency of
hereditary forms or multifocal disease.